your best partner for pet healthcare · 22 | leshimania ab leptospira ab b. abortus ab 23 |...
TRANSCRIPT
No. 206, Biotech Business IC, Dankook Univ., San-29, Anseo-dong, Dongnam, Cheonan, Chungnam 330-714 KoreaTel +82-41-523-8990 Fax +82-41-523-8991 [email protected] www.genbody.co.krCopyright GenBody Inc. 2016 All Rights Reserved.
Your Best Partner For Pet Healthcare
Global Leader of
Animal Diagnostics
2016/17MADE IN KOREA
GenBody, a global leader of animal diagnosisWe bring the innovative technologies to animal health and life!
GenBody Inc. is an R&D-orientated diagnostic company founded in 2012 in South Korea. At GenBody Inc., we
are dedicated to the fields of research, development, and quality control. We are the leading manufacturer
of various in vitro diagnostic products for animals and humans, specializing in various rapid diagnostic tests
(RDTs) and quantitative analyzing systems. We manufacture and supply raw materials and finished
products for RDT and ELISA exclusively in our labs at GenBody Inc., so that we can provide our customers
consistant high quality products and better service. We have recently developed new analyzing machines for
pet diagnosis, the qGB Analyzer and the F-qGB Analyzer, allow for easy and efficient interpretation.
is a biotechnology company manufacturing animal and human diagnostics. Through
in-depth research & development, we produce products of the highest quality.
is the logo of GenBody Inc., designed by the founder of company.
The shape of our logo 'GB' are the initials for 'Genbody'. The Y shape in the center also
symbolizes the antibody the immune system produces.
are the mascots that represent all animal diagnostic products manufactured by GenBody Inc.
Develop differentiated technologies from others.
Manufacture the highest quality products.
Provide the best customer service & satisfaction.
Devote consistent research and development for the improvement of human & animal health.
Our mission
P R O D U C T R A N G E
CONTENTS
05 | CPV Ag CCV Ag
06 | CCV/CPV Ag
07 | CDV Ag
08 | CIV Ag CAV2 Ag
09 | CDV/CIV Ag CDV/CAV2 Ag
10 | CHW Ag
11 | B. canis Ab E. canis Ab
12 | Canine IgE
13 | CPV Ab CDV Ab
14 | FPV Ag FCoV Ag
15 | FHV Ag
16 | FIV Ab FIV Ag/Ab 3.0
17 | FeLV Ag FeLV Ag/FIV Ab
18 | Giardia Ag
19 | Tg Ab Tg IgM/IgG 4.0
20 | cTnI D-Dimer BNP
21 | Rota Ag
22 | Leshimania Ab Leptospira Ab B. abortus Ab
23 | MERS-CoV Ag
24 | Neo Skin Vet
25 | Urine Strips For Veterinary
To
be a
co
mp
an
y to
cre
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a p
len
tifu
l life
Rapid Test for CPV Ag and CCV Ag
GenBody CPV Ag and GenBody CCV Ag is a chromatographic immunoassay kit for rapid detection of canine parvovirus antigen
(CPV Ag) canine coronavirus antigen (CCV Ag) in stool specimen from dogs, respectively.
1. GenBody test device individually
foil-pouched with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
CPV Ag
CCV Ag
Canine parvovirus (CPV) is a highly contagious disease, characterized by bloody diarrhea, which can
be fatal. Parvovirus can overtake a dog within hours of the first symptoms and result in death within
48 -72 hours. Even dogs which have been vaccinated against parvovirus still contact the disease.
CPV is marked by a variety of symptoms which can include severe diarrhea-sometimes dark or
bloody, vomiting, lack of energy, depression, dehydration and fever.
Canine coronavirus (CCV) is a virus of the family Coronaviridae that causes a highly contagious
intestinal disease worldwide in dogs. The virus invades and replicates in the villi of the small
intestine. Intestinal disease may be related to virus-induced apoptosis (programmed cell death) of
cells of the epithelial mucosa of the small intestine. A more serious complication of CCV occurs
when the dog is also infected with canine parvovirus. Coronavirus infection of the intestinal villi
makes the cells more susceptible to parvovirus infection.
GenBody CPV Ag GenBody CCV Ag
Specimen Feces Feces
Diagnostic target Canine parvovirus antigen Canine coronavirus antigen
Sensitivity 99.9% (vs. PCR) 99.0% (vs. PCR)
Specificity 99.0% (vs. PCR) 98.5% (vs. PCR)
Analytical sensitivity 10 HAU/ml 4x103 TCID50/ml
General Information
Material Provided
Ordering Information
C 2 1
C T
CPV Ag C
PV Ag C
P
CPV Ag C
PV Ag C
CPV Ag C
PV Ag C
PCP
CPV Ag C
PV Ag C
CPV Ag C
PV Ag C
C 2 1
C T
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
C 2 1
C T
GenBody CPV Ag or CCV Ag
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
6X
Reading
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
C 2 1
C T
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
C 2 1
C T
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
Negative
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
C 2 1
C T
Positive Invalid
20 Tests/Kit
20
30
2
Canine Parvovirus Antigen (CPV Ag) TestCPV AgOnly for veterinary useStore at 2~30
Rapid detection kit for canine parvovirusantigen (CPV Ag) in stool specimen.
Technologies for nature & human
206, Biotech Biz IC, San-29, Anseo-dong, Dongnam-gu, Cheonan, Chungnam 330-714 KoreaTel :+82-41-523-8990, Fax : +82-41-523-8991, Website: www.genbody.co.kr
Test Procedure & Interpretation
qGB Analyzer
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CPV Ag CPVAG010 Device 1 Test device x 20/kit 24 M
GenBody CCV Ag CCVAG010 Device 1 Test device x 20/kit 24 M
Gen
Bo
dy T
ech
no
log
ies fo
r natu
re &
hu
man
06
GenBody CCV/CPV Ag is a rapid immunochromatographic test for the differential detection of canine coronavirus antigen (CCV
Ag) and canine parvovirus antigen (CPV Ag) in stool specimen from dogs, simultaneously.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
One step combo test for the differential detection of CPV Ag and
CCV Ag in canine feces.
Rapid Test for CPV Ag and CCV Ag
CCV/CPV AgWorld Best Product
GenBody CCV/CPV Ag
Specimen Feces
Diagnostic target Canine parvovirus antigen Canine coronavirus antigen
Sensitivity 99.9% (vs. PCR) 99.0% (vs. PCR)
Specificity 99.0% (vs. PCR) 98.5% (vs. PCR)
Analytical sensitivity 10 HAU/ml 4x103 TCID50/ml
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CCV/CPV AgCCPAG010 Device 1 Test device x 10/kit 24 M
CCPAG020 Device 1 Test device x 20/kit 24 M
General Information
Material Provided
Ordering Information
CPV Ag C
PV Ag C
P
CPV Ag C
PV Ag C
CPV Ag C
PV Ag C
PCP
CPV Ag C
PV Ag C
CPV Ag C
PV Ag C
C 2 1
C T
CP
V A
g C
PV
Ag
CC
PV
Ag
CP
VA
gC
CP
V A
g C
PV
Ag
CCC
PV
Ag
CP
VA
gC
CP
VA
gC
PV
Ag
C
C 2 1
C T
GenBody CCV/CPV Ag
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
6X
Negative PositiveCCV Ag
PositiveCPV Ag
Invalid
Test Procedure & Interpretation
qGB Analyzer
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
Rapid Test for CDV Ag
Canine distemper is a contagious and serious viral illness with no known cure. The
disease affects dogs, and certain species of wildlife, such as raccoons, wolves, foxes,
and skunks. The common house pet, the ferret, is also a carrier of this virus. Canine
distemper belongs to the Morbillivirus class of viruses, and is a relative of the measles
virus, which affects humans, the Rinderpest virus that affects cattle, and the Phocine
virus that causes seal distemper.
All are members of the Paramyxoviridae family. Young, unvaccinated puppies and non-
immunized older dogs tend to be more susceptible to the disease.
CDV AgWorld Best Product
GenBody CDV Ag is a immunochromatographic test for rapid detection of canine distemper virus antigens in secretions of eye
mucus (the conjunctives) and nasal discharge from canine.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
GenBody CDV Ag
Specimen Secretion of eye mucus(the conjunctives) and nasal discharge
Diagnostic target Canine distemper virus antigens
Sensitivity 99.2% (vs. Nested PCR)
Specificity 99.5% (vs. Nested PCR)
Analytical sensitivity 102.3TCID50/ml
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CDV AgCDVAG010 Device 1 Test device x 10/kit 24 M
CDVAG020 Device 1 Test device x 20/kit 24 M
General Information
Material Provided
Test Procedure & Interpretation
Ordering Information
GenBody CDV Ag
CDV Ag
CDV
Ag C
D
CDV Ag
CDV
Ag C
CDV Ag
CDV
Ag C
DCD
CDV Ag
CDV
Ag C
CDV Ag
CDV
Ag C
C 2 1
C T
CD
V A
g C
DV
Ag
C
CD
VA
gC
DV
Ag
CC
DV
Ag
C
DV
Ag
CC
CD
VA
gC
DV
Ag
CC
DV
Ag
CD
VA
gC
C 2
1
C T
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
Negative
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
Positive
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
Invalid
6X
20 Tests/Kit
Canine Distemper Virus Antigen (CDV Ag) TestCDV Ag
Only for veterinary use
Store at 2~30
Rapid detection kit for canine distemper virus
antigen (CDV Ag) in body secretions.
Technologies for nature & human
P ki U it Sh lf Lif
Negative Positive Invalid
qGB Analyzer
Canine influenza virus (CIV) is a recently emergent pathogen of dogs that has caused highly
contagious respiratory disease in racing Greyhounds, pet dogs, and shelter animals.
Canine adenovirus type 2 (CAV2) causes respiratory disease in dogs and is one of the
infectious agents commonly associated with canine infectious tracheobronchitis, which is also
known as “kennel cough”. Canine infectious tracheobronchitis is usually spread through
coughing. Dogs that are around other dogs, such as at boarding facilities and dog parks, are at
increased risk for infection.
Rapid Test for CIV Ag and CAV2 Ag
CIV Ag
CAV2 Ag
GenBody CIV Ag is a rapid test for for qualitative detection of canine influenza virus antigens in secretions of eye mucus (the
conjunctives) and nasal discharge from canine. GenBody CAV2 Ag is a rapid test for the detection of canine adenovirus type 2 in
body secretions and nasal specimens from dogs.
1. GenBody test device individually
foil-pouched with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CIV Ag CIVAG010 Device 1 Test device x 10/kit 24 M
GenBody CAV2 Ag CAV2AG10 Device 1 Test device x 10/kit 24 M
General Information
Material Provided
Ordering Information
Gen
Bo
dy T
ech
no
log
ies fo
r natu
re &
hu
man
GenBody CIV Ag GenBody CAV2 Ag
Specimen Secretion of eye mucus(the conjunctives) and nasal discharge
Diagnostic target Canine influenza virus antigens Canine adenovirus 2 antigens
Sensitivity 90.5% (vs. PCR) 97.0% (vs. PCR)
Specificity 99.9% (vs. PCR) 98.0% (vs. PCR)
Analytical sensitivity 16 HAU/ml 1.2 s/CO
GenBody CIV Ag or GenBody CAV2 Ag
CIV A
g C
IV A
g C
IV A
CIV A
g C
IV A
g C
IV
CIV A
g C
IV A
g C
IVCIV
CIV A
g C
IV A
g C
IV
CIV A
g C
IV A
g C
IV
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Negative
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Positive
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Invalid
GenBody CIV Ag
GenBody CAV2 Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
Negative
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
Positive
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
Invalid
Test Procedure & Interpretation
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
One step combo test for the differential detection of CDV Ag, CIV Ag,
and CAV2 Ag in canine.
CDV/CIV Ag
CDV/CAV2 Ag
Rapid Test for CDV/CIV Ag and CDV/CAV2 Ag
GenBody CDV/CIV Ag and CDV/CAV2 Ag is an immunochromatographic test for rapid detection of canine distemper virus
antigens (CDV Ag)/canine influenza virus antigens (CIV Ag) and canine distemper virus antigens (CDV Ag)/canine adenovirus 2
antigens (CAV2 Ag) in secretions of eye mucus (the conjunctives) and nasal discharge from canine, respectively.
GenBody CDV/CIV Ag GenBody CDV/CAV2 Ag
Specimen Secretion of eye mucus(the conjunctives) and nasal discharge
Diagnostic target CDV Ag and CIV Ag CDV Ag and CAV2 Ag
Sensitivity 99.2%/90.5% 99.2%/97.0%
Specificity 99.5%/99.9% 99.5%/98.0%
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CDV/CIV Ag CDIVAG10 Device 1 Test device x 10/kit 24 M
GenBody CDV/CAV2 Ag CDAVAG10 Device 1 Test device x 10/kit 24 M
1. GenBody test device individually
foil-pouched with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
Ordering Information
Test Procedure & Interpretation
Material Provided
General Information
GenBody CDV/CIV Ag or GenBody CDV/CAV2 Ag
CDV Ag
CDV A
g C
D
CDV Ag
CDV A
g C
CDV Ag
CDV A
g C
DCD
CDV Ag
CDV A
g C
CDV Ag
CDV A
g C
C 2 1
C T
CIV A
g C
IV A
g C
IV
CIV A
g C
IV A
g C
IV
CIV A
g C
IV A
g C
IVCIV
CIV A
g C
IV A
g C
IV
CIV A
g C
IV A
g C
IV
C 2 1
C T
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
6X
GenBody CDV/CIV Ag
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Invalid
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
Negative
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
CDV AgPositive
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIVV
CIV
Ag
CIV
Ag
CIV
CIV
Ag
CIV
Ag
CIV
C 2 1
C T
CIV AgPositive
GenBody CDV/CAV2 Ag
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
Invalid
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
Negative
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
CDV AgPositive
CD
V A
g C
DV
Ag
CC
DV
Ag
CD
VA
gC
CD
V A
g C
DV
Ag
CCC
DV
Ag
CD
VA
gC
CD
VA
gC
DV
Ag
C
C 2 1
C T
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Agg
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
CA
V2
Ag
C 2 1
C T
CAV2 AgPositive
Heartworms parasite is that live inside the dog's heart. These types of worms are called
Dirofilaria immitis. Heartworms are transmitted via the mosquito as the carrier host.
Dogs get heartworms when an infected mosquito bites them. Severe infestation can
cause sudden death as heartworms can obstruct the heart and blood vessels leading to
high blood pressure and causing heart failure. The symptoms of heartworms are
coughing, weight loss and apathy.
Rapid Test for CHW Ag
GenBody CHW Ag is a rapid test for for qualitative detection of Dirofilaria immitis antigen in canine whole blood, serum or
plasma.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in dropping bottle
3. Disposable dropper
4. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CHW AgCHWAG010 Device 1 Test device x 10/kit 24 M
CHWAG020 Device 1 Test device x 20/kit 24 M
General Information
Material Provided
Ordering Information
Test Procedure & Interpretation
GenBody CHW Ag
Specimen Whole blood, serum, plasma from dogs
Diagnostic target Dirofilaria immitis antigen
Sensitivity 96.0% (vs. PCR)
Specificity 99.0% (vs. PCR)
Analytical sensitivity 5 ng/ml
Gen
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GenBody CHW Ag
Take a blood sample
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
C 2 1
C T
Load 1 drop (30㎕)of sample solution
5~10minutes
CHW Ag CHW AgCHW Ag CHW AgCHW Ag CHW AgCHW Ag CHW AgCHW Ag CHW Ag
C 2 1
C T
Reading
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
CHW A
g CHW
Ag
C 2 1
C T
Load 2 drops (60㎕)of Assay solution
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
WA
gC
HW
Ag
C 2 1
C T
Negative
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
WA
gC
HW
Ag
C 2 1
C T
Positive
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
WA
gC
HW
Ag
C 2 1
C T
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
W A
g C
HW
Ag
CH
WA
gC
HW
Ag
CH
WA
gC
HW
Ag
C 2 1
C T
Invalid
CHW AgWorld Best Product
qGB Analyzer
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
Canine brucellosis, caused by Brucella canis (B. canis), is an important cause of
reproductive failure, particularly in kennels. This organism causes abortions,
stillbirths, epididymitis, orchitis and sperm abnormalities in dogs. Although
dogs that have been spayed or neutered do not have reproductive signs, they
occasionally develop other conditions such as ocular disease and
discospondylitis.
Ehrlichia canis (E. canis) is an obligate, intracellular bacterium that acts as the
causative agent of Ehrlichiosis, a disease most commonly affecting canine
species. Animals infected with E. canis may experience a combination of signs
including but not limited to: fever, lethargy, weight loss, lymphadenopathy,
edema of the appendages, discharge from nose and eyes, and seizures.
B. canis Ab
E. canis Ab
Rapid Test for B. canis Ab and E. canis Ab
GenBody B. canis Ab and GenBody E. canis Ab is an immunochromatographic test for rapid detection of the antibodies to
Brucella canis and to Ehrlichia canis in the serum, plasma, and whole blood from dogs, respectively.
GenBody B. canis Ab GenBody E. canis Ab
Specimen Serum, plasma, and whole blood
Diagnostic target B. canis antibodies E. canis antibodies
Sensitivity 98.0% (vs. IFA) 98.0% (vs. IFA)
Specificity 99.9% (vs. IFA) 99.8% (vs. IFA)
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody B.canis Ab BCAAB010 Device 1 Test device x 10/kit 24 M
GenBody E.canis Ab ECAAB010 Device 1 Test device x 10/kit 24 M
1. GenBody test device individually
foil-pouched with a desiccant
2. Assay solution in dropping bottle
3. Disposable 10 capillary tube
4. Instruction manual for use
Ordering Information
Material Provided
General Information
Test Procedure & Interpretation
GenBody B. canis Ab or GenBody E. canis Ab
B. can
is Ab B
. can
is
B. can
is Ab B
. can
is
B. can
is Ab B
. can
isnis
B. can
is Ab B
. can
i
B. can
is Ab B
. can
is
C 2 1
C T
Load 10㎕of specimen
5~10minutes
E. c
anis
Ab
E. c
ani
Eca
nis
Ab
Eca
ni
E. c
anis
Ab
E. c
anii
Eca
nis
Ab
Eca
ni
Eca
nis
Ab
Eca
ni
C 2 1
C T
Reading
GenBody B. canis Ab
B. c
anis
Ab
B. c
anB
can
isA
bB
can
B. c
anis
Ab
B. c
anB
can
isA
bB
can
Bca
nis
Ab
Bca
n
C 2 1
C T
Negative
B. c
anis
Ab
B. c
anB
can
isA
bB
can
B. c
anis
Ab
B. c
anB
can
isA
bB
can
Bca
nis
Ab
Bca
n
C 2 1
C T
B. canis AbPositive
B. c
anis
Ab
B. c
anB
can
isA
bB
can
B. c
anis
Ab
B. c
anB
can
isA
bB
can
Bca
nis
Ab
Bca
n
C 2 1
C T
B. c
anis
Ab
B. c
anB
can
isA
bB
can
B. c
anis
Ab
B. c
anB
can
isA
bB
can
Bca
nis
Ab
Bca
n
C 2 1
C T
Invalid
GenBody E. canis Ab
E. c
anis
Ab
E. c
ani
Eca
nis
Ab
Eca
ni
E. c
anis
Ab
E. c
anii
Eca
nis
Ab
Eca
ni
Eca
nis
Ab
Eca
ni
C 2 1
C T
Negative
E. c
anis
Ab
E. c
ani
Eca
nis
Ab
Eca
ni
E. c
anis
Ab
E. c
anii
Eca
nis
Ab
Eca
ni
Eca
nis
Ab
Eca
ni
C 2 1
C T
E. canis AbPositive
E. c
anis
Ab
E. c
ani
Eca
nis
Ab
Eca
ni
E. c
anis
Ab
E. c
anii
Eca
nis
Ab
Eca
ni
Eca
nis
Ab
Eca
ni
C 2 1
C T
E. c
anis
Ab
E. c
ani
Eca
nis
Ab
Eca
ni
C 2 1
C T
Invalid
Load 3 dropsof Assay solution
B. can
is Ab B
. can
is
B. can
is Ab B
. can
is
B. can
is Ab B
. can
isnis
B. can
is Ab B
. can
i
B. can
is Ab B
. can
is
C 2 1
C T
E. c
anis
Ab
E. c
aan
is A
b
nii
Eca
nis
Ab
Eca
can
isA
bn
iE
can
isA
bE
caca
nis
An
i
C 2 1
CC T
qGB Analyzer
The immune response, which normally protects the dog against infection and
disease, can actually be harmful to the body. The immune reactions involved in
allergies are quite complex. Most reactions involve an antibody in the blood called
“Immunoglobulin E (IgE)”. In an allergic reaction the allergen protein molecules
combine with IgE antibody molecules and attach to a type of cell called “mast
cell”, found in many tissues throughout the body. When these cells are attached
to the allergen, they break up and release potent chemicals such as histamines
that cause local inflammation (redness, welling and itching). This inflammation
cause the various signs associated with an allergic reaction. Therefore, Canine
IgE titers are very important for health prediction in dog.
Canine IgE
Rapid Test for Canine IgE
GenBody IgE is a rapid chromatographic immunoassay kit for detecting the level of IgE in serum and plasma from dog.
1. GenBody test device individually foil-pouched
with a desiccant
2. Disposable 10 capillary tube
3. Disposable dropper
4. Assay solution in tube
5. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody Canine IgE CNIGE010 Device 1 Test device x 10/kit 24 M
CNIGE020 Device 1 Test device x 20/kit 24 M
General Information
Material Provided
Ordering Information
Test Procedure & Interpretation
GenBody Canine IgE
Specimen Serum and plasma from dogs
Diagnostic target Canine Immunoglobulin E (IgE)
Sensitivity 98.0% (vs. ELISA)
Specificity 98.5% (vs. ELISA)
Gen
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Canine
IgE C
anine
Ig
Canine
IgE C
anine
I
Canine
IgE C
anine
Igne
Ig
Canine
IgE C
anine
I
Canine
IgE C
anine
I
GenBody Canine IgE
Add serumor plasma (10㎕) Mixing Add 3 drops
5~10minutes
E. canis Ab E. caniE canis Ab E caniE. canis Ab E. caniiE canis Ab E caniE canis Ab E cani
C 2 1
C T
Reading
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
inee
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
C 2 1
C T
Negative
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
inee
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
C 2 1
C T
Positive
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
inee
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
C 2 1
C T
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
inee
Can
ine
IgE
Can
ine
Can
ine
IgE
Can
ine
C 2 1
C T
InvalidNegative Positive Invalid
qGB Analyzer
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
Canine parvovirus (CPV) is the major viral disease in dogs in the world, which cause
gastroenteritits resulting to severe enteritis and lymphopenia having high motality in dogs.
CPV antibody can give seroprotection against its infection in dogs. Therefore, CPV antibody
titers are very important in the vaccination programs and health prediction in dogs.
Canine distemper virus (CDV) induces a highly contagious, systemic, and often fatal disease
in domestic dogs as well as in a broad, and seemingly expanding, range of wild carnivore
species. Modified live-attenuated CDV vaccines are available for use in dogs and in general,
they efficiently induce protective immunity. However, even in domestic dog populations in
which a broad vaccination coverage is maintained, sporadic cases and outbreaks of canine
distemper occasionally occur. Therefore, the examination of the CDV antibody in dog blood
is very important to determine the ideal time point for vaccination of a pup, to evaluate
vaccination success, and to determine the diagnosis and prognosis of acute CDV infections.
Rapid Test for CPV Ab and CDV Ab
GenBody CPV Ab and GenBody CDV Ab is an immunochromatographic test for rapid & quantitative detection of the antibodies to
canine parvovirus (CPV) and canine distemper virus (CDV) in the serum and plasma from dogs, respectively.
GenBody CPV Ab GenBody CDV Ab
Specimen Serum and plasma
Diagnostic target CPV antibodies CDV antibodies
Analytical sensitivity 1:10 HI 1:16 NA
*HI, hemagglutination inhibition;**NA, neutralization assay
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in dropping bottle
3. Disposable dropper
4. Instruction manual for use
*qGB Analyzer for quantitative reading
*Color Index for semi-quantitative reading
Material Provided
General Information
CPV AbCDV Ab
World First Real Quantitative
CDV Ab CDV Ab CCDV Ab CDV Ab CCDV Ab CDV Ab CCCDV Ab CDV Ab CCDV Ab CDV Ab C
C 2 1
C T
Interpretation Table for CDV Ab
Color ColorIndex
Interpretation Titer of NA*Score
0a No band or trace
No or lessimmunity
1:16
1a1:32
2a
Sero-protective
1:128
3a1:256
b4a 256
b
b
b
b
ColorScore
Interpretation Titer of HI*
No band or trace1:10
1:80
1:320
1:640
1:640
0a
1a
2a
3ab
4ab
b
b
b
Interpretation Table for CPV Ab
ColorIndex
No or lessimmunity
Sero-protective
*HI, haemagglutination inhibition; NA, neutralization assay.
1) Quantitative: qGB Analyzer 2) Semi-quantitative: Color Index
CD
V A
b C
DV
Ab
CC
DV
Ab
CD
VA
bC
CD
V A
b C
DV
Ab
CCC
DV
Ab
CD
VA
bC
CD
VA
bC
DV
Ab
CC
2 1
C T
Reading
GenBody CPV Ab or GenBody CDV Ab
CDV Ab
CDV
Ab C
D
CDV Ab
CDV
Ab C
Load 1 drop (30㎕)of serum or plasma
CDV Ab
CDV
Ab C
D
CDV Ab
CDV
Ab C
CDV Ab
CDV
Ab C
DCD
CDV Ab
CDV
Ab C
CDV Ab
CDV
Ab C
Add 2 drops (60㎕)of serum or plasma
20 minutes
C T
For CPV Ab, CDV Ab, cTnI, D-Dimer, BNP
Acuc
ra t! el bail eR & e
Test Procedure & Interpretation
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody CPV Ab CPVAB010 Device 1 Test device x 10/kit 24 M
GenBody CDV Ab CDVAB010 Device 1 Test device x 10/kit 24 M
GenBody CPV/CDV Ab CPDAB010 Device 1 Test device x 10/kit 24 M
1) Quantitative: qGBqGB Ananalyzelyzer
Ordering Information
Gen
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Panleukopenia due to feline parvovirus (FPV) is one of the most important infectious
diseases of cats in the world. The clinical symdromes are gastroenteritis, manifested as
diarrhea, emesis, anorexia, and abdominal tenderness.
Coronaviruses that infect cats are called 'feline coronaviruses (FCoV). In cats, FCoV
most frequently causes gastrointestinal infections, but in unusual cases (with a mutated
form of the virus) it can spread through the body and cause FIP.
FPV Ag
FCoV Ag
Rapid Test for FPV Ag and FCoV Ag
GenBody IgE is a rapid chromatographic immunoassay kit for detecting the level of IgE in serum and plasma from dog.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
General Information
Material Provided
Test Procedure & Interpretation
Ordering Information
GenBody FPV Ag GenBody FCoV Ag
Specimen Feline feces
Diagnostic target FPV antigens FCoV antigens
Sensitivity 98.0% (vs. PCR) 96.0% (vs. PCR)
Specificity 99.5% (vs. PCR) 99.0% (vs. PCR)
Analytical sensitivity 10 HAU/ml 5x103 TCID50/ml
FP
V A
g F
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
FP
V A
g F
PV
Ag
FPP
FP
VA
gF
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
C 2 1
C T
Negative
FP
V A
g F
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
FP
V A
g F
PV
Ag
FPP
FP
VA
gF
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
C 2 1
C T
Positive
FP
V A
g F
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
FP
V A
g F
PV
Ag
FPP
FP
VA
gF
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
C 2 1
C T
FP
V A
g F
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
FP
V A
g F
PV
Ag
FPP
FP
VA
gF
PV
Ag
FP
FP
VA
gF
PV
Ag
FP
C 2 1
C T
Invalid
GenBody FPV Ag or GenBody FCoV Ag
FPV Ag F
PV Ag F
PV
FPV Ag F
PV Ag F
PV
FPV Ag F
PV Ag F
PVFPV
FPV Ag F
PV Ag F
PV
FPV Ag F
PV Ag F
PV
C 2 1
C T
FPV
Ag
FPV
Ag
FPFP
VA
gFP
VA
gFP
FPV
Ag
FPV
Ag
FPPFP
VA
gFP
VA
gFP
FPV
Ag
FPV
Ag
FP
C 2 1
C T
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
6X
Negative Positive Invalid
qGB Analyzer
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody FPV Ag FPVAG010 Device 1 Test device x 10/kit 24 M
GenBody FCoV Ag FCOAG010 Device 1 Test device x 20/kit 24 M
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
Feline herpesvirus type 1 (FHV1) is an important pathogenic agent that causes
feline viral rhinotracheitis, which is a highly infectious upper respiratory tract
infection of felids. The virus is readily transmitted between cats through:
direct contact (through contact with saliva, ocular or nasal secretions), inhalation
of sneeze droplets, sharing or food bowls and litter trays, and a contaminated
environment (including bedding and grooming aids). This infection is often fatal to
kittens, but adult cats usually survive and exhibit lifelong latency.
Rapid Test for FHV Ag
GenBody FHV Ag is a immunochromatographic test for rapid detection of feline herpes virus antigens in secretion of eye mucus
(the conjunctives) and nasal discharge from canine.
GenBody FHV Ag
Specimen Secretion of eye mucus(the conjunctives) and nasal discharge
Diagnostic target Feline herpes virus antigens
Sensitivity 99.0% (vs. Nested PCR)
Specificity 99.6% (vs. Nested PCR)
*HI, hemagglutination inhibition;**NA, neutralization assay
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
Material Provided
General Information
FHV AgWorld First Product
Ordering Information
FH
V A
g F
HV
Ag
F
FH
VA
gF
HV
Ag
FF
HV
Ag
F
HV
Ag
FF
FH
VA
gF
HV
Ag
FF
HV
Ag
FH
VA
gF
C 2 1
C T
Negative
FH
V A
g F
HV
Ag
F
FH
VA
gF
HV
Ag
FF
HV
Ag
F
HV
Ag
FF
FH
VA
gF
HV
Ag
FF
HV
Ag
FH
VA
gF
C 2 1
C T
Positive
FH
V A
g F
HV
Ag
F
FH
VA
gF
HV
Ag
FF
HV
Ag
F
HV
Ag
FF
FH
VA
gF
HV
Ag
FF
HV
Ag
FH
VA
gF
C 2 1
C T
FH
V A
g F
HV
Ag
F
FH
VA
gF
HV
Ag
FF
HV
Ag
F
HV
Ag
FF
FH
VA
gF
HV
Ag
FF
HV
Ag
FH
VA
gF
C 2 1
C T
Invalid
GenBody FHV Ag
FHV
Ag F
HV Ag
FH
FHV
Ag F
HV Ag
FH
FHV
Ag F
HV Ag
FHFH
FHV
Ag F
HV Ag
FH
FHV
Ag F
HV Ag
FH
C 2 1
C T
FH
V A
g F
HV
Ag
F
FH
VA
gF
HV
Ag
FF
HV
Ag
F
HV
Ag
FF
FH
VA
gF
HV
Ag
FF
HV
Ag
FH
VA
gF
C 2
1
C T
Specimen Mix Take the solution Load 3~4 drops ofsample solution
5~10minutes
Reading
6X
Test Procedure & Interpretation
Negative Positive Invalid
qGB Analyzer
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody FHV AgFHVAG010 Device 1 Test device x 10/kit 24 M
FHVAG020 Device 1 Test device x 20/kit 24 M
Gen
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FIV is a complex retrovirus of the genus Lentivirus. There are at least
five different subtypes (clades; A, B, C, D, E) of FIV found in domestic and
wild felids throughout the world. FIV primarily infects lymphocytes and
integrates its genetic information into the genomic DNA of infected
lymphocytes. Over time, there is a selective and progressive loss of
CD4+ T-helper lymphocytes, which primarily results in impaired cell-
mediated immunity.
Rapid Test for FIV Ag and Ab Combo Test
GenBody FIV Ab is an immunochromatographic test for rapid detection of the antibodies to feline immunodeficiency virus in the
serum, plasma, and whole blood from dogs. GenBody FIV Ag/Ab 3.0 is the world first rapid diagnostic kit for the detection of
antigens and antibodies of feline immunodeficiency virus in the bloods
GenBody FIV Ab GenBody FIV Ag/Ab 3.0
Specimen Serum, plasma, and whole blood from cats
Diagnostic target FIV antibodies FIV antigen and antibodies
Sensitivity 99.5% (vs. ELISA) 95% for Ag and 99.5% for Ab (vs.ELISA)
Specificity 99.9% (vs. ELISA) 99.9% for both (vs. ELISA)
Analytical sensitivity 1.5 s/CO 5 ng/ml and 1.5 s/CO
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody FIV Ab FIVAB010 Device 1 Test device x 10/kit 24 M
GenBody FIV Ag/Ab FIVAGB10 Device 1 Test device x 10/kit 24 M
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in dropping bottle
3. Disposable 10 capillary tube
4. Instruction manual for use
Material Provided
General Information
Ordering Information
FIV AbFIV Ag/Ab 3.0
World First Product
GenBody FIV Ag/Ab 3.0
Negative
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FIV AgPositive
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
Invalid
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
C 2
1
C T
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FIV AbPositive
GenBody FIV Ab
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2 1
C T
Negative
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2 1
C T
Positive
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2 1
C T
FIV
Ag
FIV
Ag
FIV
AF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
AAF
IVA
gF
IVA
gF
IVA
FIV
Ag
FIV
Ag
FIV
A
C 2 1
C T
Invalid
GenBody FIV Ag/Ab
FIV A
b FIV
Ab F
IV A
b
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
bV
Ab
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
C 2 1
C T
FIV A
g FIV
Ag F
IV A
g
FIV A
g FIV
Ag F
IV A
FIV A
g FIV
Ag F
IV A
gV
Ag
FIV A
g FIV
Ag F
IV A
FIV A
g FIV
Ag F
IV A
C 2 1
C T
Load 10㎕of specimen
5~10minutes
FIV Ag FIV Ag FIV AFIV Ag FIV Ag FIV AFIV Ag FIV AgFIV Ag FIV AgFIV Ag FIV Ag
C 2 1
C T
FIV Ab FIV Ab FIV AFIV Ab FIV Ab FIV AFIV Ab FIV AbFIV Ab FIV AbFIV Ab FIV Ab
C 2 1
C T
ReadingLoad 3 dropsof Assay solution
FIV A
b FIV
Ab F
IV A
b
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
bV
Ab
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
C 2 1
C T
FIV A
g FIV
Ag F
IV A
g
FIV A
g FIV
Ag F
IV A
FIV A
g FIV
Ag F
IV A
gV
Ag
FIV A
g FIV
Ag F
IV A
FIV A
g FIV
Ag F
IV A
C 2 1
C T
Test Procedure & Interpretation
FIV
Ag
FIV
Ag
FIV
AF
AF
IVA
gF
IVA
gF
IVA
VA
FIV
Ag
FIV
Ag
FIV
AV
A
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 22
1
CC T
g FIV AAg FIV Ag FIV A
bb FIV AAb FIV Ab FIV A
qGB Analyzer
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
Feline leukemia virus (FeLV) is one of the most important
infectious pathogens that causes death in cats and is broadly
spread worldwide. FeLV was discovered among cats that lived in a
cluster-household where several animals had developed
lymphosarcoma. The virus is an enveloped, positive single-
stranded RNA retrovirus. Cats are usually infected by direct
contact with infected cats, mostly via oronasal exposure to saliva
and nasal secretions containing high levels of the virus especially
through mutual grooming and sharing food dishes or water bowls.
FeLV Ag
FeLV Ag/FIV Ab
Rapid Test for FeLV Ag and FIV Ab Combo Test
GenBody FeLV Ag is a rapid chromatographic immunoassay kit for detecting feline leukemia virus antigens in serum, plasma,
and whole blood from dog. GenBody FeLV Ag/FIV Ab is a combo test for detecting FeLV antigens and FIV antibodies in the feline
whole bloods.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in dropping bottle
3. Disposable 10 capillary tube
4. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody FeLV Ag FELAG010 Device 1 Test device x 10/kit 24 M
GenBody FeLV Ag/FIV Ab FELFIV10 Device 1 Test device x 10/kit 24 M
General Information
Material Provided
Test Procedure & Interpretation
Ordering Information
GenBody FeLV Ag GenBody FeLV Ag/FIV Ab
Specimen Serum, plasma, and whole blood from cats
Diagnostic target FeLV antigens FeLV antigens and FIV antibodies
Sensitivity 95.2% (vs. PCR) 95.2% for FeLV Ag and 99.5% for FIV Ab
Specificity 98.0% (vs. PCR) 98.0% for FeLV Ag and 99.9% for FIV Ab
GenBody FeLV Ag
FeL
V A
g F
eLV
Ag
FF
eLV
Ag
FeL
VA
gF
FeL
V A
g F
eLV
Ag
FFF
eLV
Ag
FeL
VA
gF
FeL
VA
gF
eLV
Ag
F
C 2 1
C T
Negative
FeL
V A
g F
eLV
Ag
FF
eLV
Ag
FeL
VA
gF
FeL
V A
g F
eLV
Ag
FFF
eLV
Ag
FeL
VA
gF
FeL
VA
gF
eLV
Ag
F
C 2 1
C T
Positive
FeL
V A
g F
eLV
Ag
FF
eLV
Ag
FeL
VA
gF
FeL
V A
g F
eLV
Ag
FFF
eLV
Ag
FeL
VA
gF
FeL
VA
gF
eLV
Ag
F
C 2 1
C T
FeL
V A
g F
eLV
Ag
FF
eLV
Ag
FeL
VA
gF
FeL
V A
g F
eLV
Ag
FFF
eLV
Ag
FeL
VA
gF
FeL
VA
gF
eLV
Ag
F
C 2 1
C T
Invalid
GenBody FeLV Ag/FIV Ab
Negative
FeL
V A
g F
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
FeL
V A
g F
eLV
Ag
FeLL
FeL
VA
gF
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FeLV AgPositive
FeL
V A
g F
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
FeL
V A
g F
eLV
Ag
FeLL
FeL
VA
gF
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
Invalid
FeL
V A
g F
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
FeL
V A
g F
eLV
Ag
FeLL
FeL
VA
gF
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FeL
V A
g F
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
FeL
V A
g F
eLV
Ag
FeLL
FeL
VA
gF
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
C 2
1
C T
FeL
V A
g F
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
FeL
V A
g F
eLV
Ag
FeLL
FeL
VA
gF
eLV
Ag
FeL
FeL
VA
gF
eLV
Ag
FeL
C 2
1
C T
FIV
Ab
FIV
Ab
FIV
AF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
AAF
IVA
bF
IVA
bF
IVA
FIV
Ab
FIV
Ab
FIV
A
C 2
1
C T
FIV AbPositive
GenBody FeLV Ag/FIV Ab
5~10minutes
FeLV Ag FeLV Ag FFeLV Ag FeLV Ag FFeLV Ag FeLVFeLV Ag FeLVFeLV Ag FeLV
C 2 1
C T
FIV Ab FIV Ab FIV AFIV Ab FIV Ab FIV AFIV Ab FIV AbFIV Ab FIV AbFIV Ab FIV Ab
C 2 1
C T
Reading
FIV A
b FIV
Ab F
IV A
b
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
bV
Ab
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
C 2 1
C T
FeLV A
g FeL
V Ag F
eL
FeLV A
g FeL
V Ag F
e
FeLV A
g FeL
V Ag F
eFe
FeLV A
g FeL
V Ag F
FeLV A
g FeL
V Ag F
e
C 2 1
C T
Load 10㎕of specimen
Load 3 dropsof Assay solution
FIV A
b FIV
Ab F
IV A
b
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
bV
Ab
FIV A
b FIV
Ab F
IV A
FIV A
b FIV
Ab F
IV A
C 2 1
C T
FeLV A
g FeL
V Ag F
eL
FeLV A
g FeL
V Ag F
e
FeLV A
g FeL
V Ag F
eFe
FeLV A
g FeL
V Ag F
FeLV A
g FeL
V Ag F
e
C 2 1
C T
C
Ab
FIV
AV
Ab
FIV
Ab
FIV
AA
Ab
FIV
AV
Ab
FIV
AF
IVA
bF
IVA
VA
bF
IVA
FIV
CC
V Ag FFV Ag FV Ag F
b FIV AAb FIV AFIV Ab FIV AA
qGB Analyzer
Gen
Bo
dy T
ech
no
log
ies fo
r natu
re &
hu
man
Giardia is a single-celled protozoan parasite that causes intestinal infections
in both dogs and cats. Dogs become infected when they ingest Giardia cysts
that may be present in water or other areas of the environment that have
been contaminated with feces.
Symptoms are more visible in puppies and younger dogs than in older dogs
and can be acute, transient, intermittent, or chronic in nature. In some cases,
dogs will exhibit diarrhea that is soft, frothy, greasy, and with a strong odor or
excessive mucus.
Rapid Test for Giardia Ag
GenBody Giardia Ag is an immunochromatographic test for rapid detection of Giardia cyst antigens in stool specimens from
dogs or cats.
GenBody Giardia Ag
Specimen Feces
Diagnostic target Giardia cyst antigens
Analytical sensitivity 100~200 cysts/100 ml
Diagnostic target 99.0% (vs. PCR)
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody Giardia AgGIAAG010 Device 1 Test device x 10/kit 24 M
GIAAG020 Device 1 Test device x 20/kit 24 M
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
Material Provided
General Information
Test Procedure & Interpretation
Ordering Information
Giardia AgC
2 1
C T
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Agg
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Negative
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Agg
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
C 2 1
C T
Positive
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Agg
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
C 2 1
C T
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Agg
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
Gia
rdia
Ag
C 2 1
C T
Invalid
GenBody Giardia Ag
Giardia
Ag Giar
dia Ag
Giardia
Ag Giar
diaA
Giardia
Ag Giar
dia A
ia A
Giardia
Ag Giar
diaA
Giardia
Ag Giar
diaA
C 2 1
C T
Gia
rdia
Ag
Gia
rdia
G
iard
iaA
gG
iard
iaG
iard
ia A
g G
iard
ia
Gia
rdia
Ag
Gia
rdia
Gia
rdia
Ag
Gia
rdia
C 2 1
C T
5~10minutes
Specimen Mix Take the solution Load 3~4 drops ofsample solution Reading
6X
Toxoplasmosis is an infection caused by the Toxoplasma gondii (T.
gondii) parasite. It is one of the most common parasitic diseases and
is known to affect nearly all warm-blooded animals and humans, but
cats are the primary living host. This parasite completes its life cycle
in cats, and they are the only mammals in which this parasite is
passed through the feces and into the environment as part of the life
cycle. However, contact with raw meat and unwashed produce is also
a very significant and well known source of human infection. Both
acute and chronic forms of toxoplasmosis exist, where the chronic
form is usually a low-grade disease without any clinical symptoms,
and the acute form is more symptomatic.
Rapid Test for FeLV Ag and FIV Ab Combo Test
GenBody Tg Ab is a rapid test for for qualitative detection of all antibodies (IgG, IgM, IgA) against T. gondii in the bloods from
cats, dogs or swine. GenBody Tg IgM/IgG 4.0 is a rapid test for the differential detection of feline IgM (T1), canine IgM (T2), and
total IgG (T3) in the bloods from cats or dogs.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in dropping bottle
3. Disposable 10 capillary tube
4. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody Tg Ab TGAB0010 Device 1 Test device x 10/kit 24 M
GenBody Tg IgM/IgG 4.0 TGMG4010 Device 1 Test device x 10/kit 24 M
General Information
Material Provided
Ordering Information
GenBody Tg Ab GenBody Tg IgM/IgG 4.0
Specimen Serum, plasma, and whole blood from cats
Diagnostic target T. gondii antibodies cat IgM, dog IgM and total IgG against T. gondii
Sensitivity 99.5% (vs. ELISA) 98% / 98% / 98%
Specificity 99.5% (vs. ELISA) 99% / 99% / 99.9%
Analytical sensitivity 0.8 s/CO 1,0/1,0/0.8 s/CO
Tg Ab
Tg IgM/IgG 4.0World First Product
To
be a
co
mp
an
y to
cre
ate
a p
len
tifu
l life
GenBody Tg Ab
GenBody Tg IgM/IgG 4.0
Tg
Ab
Tg
Ab
Tg
Ab
TT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
TTT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
T
C 2 1
C T
Negative
Tg
Ab
Tg
Ab
Tg
Ab
TT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
TTT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
T
C 2 1
C T
Positive
Tg
Ab
Tg
Ab
Tg
Ab
TT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
TTT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
T
C 2 1
C T
Tg
Ab
Tg
Ab
Tg
Ab
TT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
TTT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
T
C 2 1
C T
Invalid
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
Negative
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
Cat IgMPositive
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
Dog IgMPositive
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
IgGPositive
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgGG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
Tg
IgM
IgG
C 2 1
C T
Invalid
GenBody Tg Ab or GenBody Tg IgM/IgG 4.0
TgAb
TgAb
TgAb
Tg
TgAb
TgAb
TgAb
T
TgAb
TgAb
TgAb
Tgb
Tg
TgAb
TgAb
TgAb
T
TgAb
TgAb
TgAb
T
C 2 1
C T
Using capillary pipette provided,add 10㎕ of serum, plasma or
whole blood into the sample well (S)
Tg
Ab
Tg
Ab
Tg
Ab
TT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
TTT
gA
bT
gA
bT
gA
bT
Tg
Ab
Tg
Ab
Tg
Ab
T
C 2
1
C T
TgAb
TgAb
TgAb
Tg
TgAb
TgAb
TgAb
T
TgAb
TgAb
TgAb
Tgb
Tg
TgAb
TgAb
TgAb
T
TgAb
TgAb
TgAb
T
C 2 1
C T
10㎕
Dispense 3 dropsof Assay solution
5~10minutes
Reading
Test Procedure & Interpretation
Gen
Bo
dy T
ech
no
log
ies fo
r natu
re &
hu
man
Cardiac troponin I (cTnI) is a thin filament-associated regulatory protein of the heart muscle and
uniquely expressed in the myocardium. cTnI is a very sensitive serum marker of physical or
metabolic myocardial injury, myocardial ischemia, or necrosis with a cardiac specificity of 100%.
cTnI is approximately 95% of total structural agreement between mammals. In normal dogs and
cats, cTnI in serum is less than 0.5 ng/ml, which is to be cut off value of the diagnostic kit, with a
different level of human cTnI (2.0 ng/ml).
D-dimer is a degradation product of cross-linked fibrin formed during activation of the
coagulation system. It is commonly used to diagnose thromboembolic disease in outpatients
suspected of having deep venous thrombosis (DVT) and pulmonary embolism (PE). By providing a
quick, non-invasive alternative to costly imaging, D-dimer has demonstrated to aid in the
detection of venous thromboembolism (VTE) in outpatients. In normal dogs and cats, D-dimer in
serum is less than 300 ng/ml, which is to be cut-off value of the diagnostic kit.
Rapid Test for cTnI, D-Dimer, and BNP
GenBody cTnI, GenBody D-Dimer, and GenBody BNP are rapid tests for the detection of cardiac troponin I (cTnI), d-dimer, and
BNP in the serum, plasma, and whole blood from dogs and cats, respectively.
GenBody cTnI GenBody D-Dimer GenBody BNP
Specimen Serum, plasma, and whole blood
Diagnostic target Cardiac troponin I D-dimer BNP
Cut off 0.5 ng/ml 100 ng/ml 0.1 ng/ml
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody cTnI/D-Dimer TNIDDM10 Device 1 Test device x 10/kit 24 M
GenBody cTnI/BNP TNIBNP10 Device 1 Test device x 10/kit 24 M
GenBody cTnI CTNI0010 Device 1 Test device x 10/kit 24 M
General Information
cTnID-DimerBNP
cTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTn
C 2 1
C T
ColorScore
Interpretation cTnI Conc. (ng/ml)
No band or trace 0 or 0.5
0.5 ~ 1.0
0a
1234
b
1.1 ~ 10.010.1 ~ 25.0
25.0
Interpretation Table for cTnIColorIndex
ColorScore
Interpretation D-Dimer Conc. (ng/ml)
No band or trace 0 or 300
301 ~ 1,000
0a
1234
b
1,001 ~ 3,0003,001 ~ 7,000
7,000
Interpretation Table for D-DimerColorIndex
Negative
Positive
Negative
Positive
Negative
Positive
ColorScore
Interpretation BNP Conc. (ng/ml)
No band or trace 0 or 0.1
0.1 ~ 2.0
0a
1234
b
2.1 ~ 10.010.1 ~ 25.0
25.0
Interpretation Table for BNPColorIndex
GenBody cTnI, GenBody D-Dimer, and GenBody BNP
1) Quantitative: qGB Analyzer 2) Semi-quantitative: Color Index
cTnl
cTnl
cTnl
cTnl
c
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
c
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
cTnl
C 2 1
C T
Load 3 drops of specimen
cTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTncTnl cTnl cTnl cTn
C 2 1
C T
Reading20 minutes
For CPV Ab, CDV Ab, cTnI, D-Dimer, BNP
Acuc
ra t! el bai leR & e
1) Quantuantitatitative:ive: qGBqGB AnaAnalyzelyzerr
1. GenBody test device individually
foil-pouched with a desiccant
2. Disposable dropper
3. Instruction manual for use
Material Provided
* qGB Analyzer for quantitative reading
* Color Index for semi-quantitative reading
Ordering Information
Test Procedure & Interpretation
Rotavirus is the most common causative virus of acute gastroenteritis and
diarrhea in canine, porcine, and bovine. Among several groups of rotavirus group A
is most prevalent and clinically important.
Rapid Test for Rotavirus Ag
GenBody Rota Ag is a rapid chromatographic immunoassay kit for detecting the rotavirus antigen in the stool specimen from
animals.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody Rota AgROTAG010 Device 1 Test device x 10/kit 24 M
ROTAG020 Device 1 Test device x 20/kit 24 M
General Information
Material Provided
Test Procedure & Interpretation
Ordering Information
GenBody Rota Ag
Specimen Feces
Diagnostic target Group A rotavirus antigen
Sensitivity 99.0% (vs. PCR)
Specificity 98.5% (vs. PCR)
Analytical sensitvity 103.5 TCID50/ml
Rota Ag
To
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GenBody Rota Ag
Specimen Take the solution
Rota
Ag Rot
a Ag
Rot
Rota
Ag Rot
a Ag
Ro
Rota
Ag Rot
a Ag
RoRo
Rota
Ag Rot
a Ag
R
Rota
Ag Rot
a Ag
Ro
C 2 1
C T
Load 3~4 drops ofsample solution
5~10minutes
Ro
ta A
g R
ota
Ag
RR
ota
Ag
Ro
taA
gR
Ro
ta A
g R
ota
Ag
RRR
ota
Ag
Ro
taA
gR
Ro
taA
gR
ota
Ag
R
C 2
1
C T
ReadingMix
6X
Ro
ta A
g R
ota
Ag
RR
ota
Ag
Ro
taA
gR
Ro
ta A
g R
ota
Ag
RRR
ota
Ag
Ro
taA
gR
Ro
taA
gR
ota
Ag
R
C 2 1
C T
Negative
Ro
ta A
g R
ota
Ag
RR
ota
Ag
Ro
taA
gR
Ro
ta A
g R
ota
Ag
RRR
ota
Ag
Ro
taA
gR
Ro
taA
gR
ota
Ag
R
C 2 1
C T
Positive
Ro
ta A
g R
ota
Ag
RR
ota
Ag
Ro
taA
gR
Ro
ta A
g R
ota
Ag
RRR
ota
Ag
Ro
taA
gR
Ro
taA
gR
ota
Ag
R
C 2 1
C T
Ro
ta A
g R
ota
Ag
RR
ota
Ag
Ro
taA
gR
Ro
ta A
g R
ota
Ag
RRR
ota
Ag
Ro
taA
gR
Ro
taA
gR
ota
Ag
R
C 2 1
C T
InvalidNegative Positive Invalid
qGB Analyzer
Gen
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hu
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Leishmania infantum is the most common and important cause of canine
leishmaniasis worldwide. Skin lesions are the most common sign associated with
clinical leishmaniasis in endemic areas and may include regional (often facial)
alopecia and non-pruritic, ulcerative, nodular, or papular dermatitis.
Canine leptospirosis, “lepto” for short, is an infection caused by at least four species
of Leptospira bacteria, or serovars. Leptospira bacteria are transmitted through
urine that contaminates water sources and can remain infectious in soil for up to
six months.
When symptoms do occur they usually appear between 4 and 12 days after
exposure to the bacteria, and can include fever, muscle pain, vomiting and diarrhea,
loss of appetite, lethargy, depression, and blood in the urine.
Rapid Test for Leishmania Ab and Leptospira Ab
GenBody Leishmania Ab and GenBody Leptospira Ab are the immunochromatographic tests for rapid detection of the antibodies
to Leshimania and to Leptospira in the serum, plasma, and whole blood from dogs, respectively. GenBody B. abortus Ab is a
rapid immunochromatographic assay kit for detecting the antibodies to B. abortus in serum, milk, and whole blood from cows.
GenBody Leishmania Ab GenBody Leptospira Ab GenBody B. abortus Ab
Specimen Serum, plasma, and whole blood
Diagnostic target Leishmania antibodies Leptospira antibodies B. abortus antibodies
Sensitivity 99.5% (vs. ELISA) 99.6% (vs. ELISA) 99.5% (vs. ELISA)
Specificity 99.8% (vs. ELISA) 99.8% (vs. ELISA) 99.8% (vs. ELISA)
Analytical sensitivity 1.2 s/CO 1.1 s/CO 1.0 s/CO
1. GenBody test device individually
foil-pouched with a desiccant
2. Assay solution in dropping bottle
3. Disposable 10 capillary tube
4. Instruction manual for use
Material Provided
General Information
Test Procedure & Interpretation
Ordering Information
Leishmania AbLeptospira AbB. abortus Ab
World Best Product
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eis
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eiL
eish
man
iaA
bL
eis
C 2 1
C T
Negative
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eis
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eiL
eish
man
iaA
bL
eis
C 2 1
C T
Positive
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eis
Lei
shm
ania
Ab
Lei
sL
eish
man
iaA
bL
eiL
eish
man
iaA
bL
eis
C 2 1
C T
Les
him
ania
Ab
Les
Les
him
ania
Ab
Les
Les
him
ania
Ab
Less
Les
him
ania
Ab
Les
Les
him
ania
Ab
Les
C 2 1
C T
Invalid
GenBody Leishmania Ab / GenBody Leptospira AbGenBody B. abortus Ab
Leish
man
ia Ab L
eish
Leish
man
ia Ab L
eis
Leish
man
ia Ab L
eish
eish
Leish
man
ia Ab L
eis
Leish
man
ia Ab L
eis
C 2 1
C T
Load 10 ㎕ of specimen
5~10minutes
Leishmania Ab LeisLeishmania Ab LeisLeishmania Ab LeisLeishmania Ab LeiLeishmania Ab Leis
Reading
Load 3 dropsof Assay solution
Leish
man
ia Ab L
eish
Leish
man
ia Ab L
eis
Leish
man
ia Ab L
eish
eish
Leish
man
ia Ab L
eis
Leish
man
ia Ab L
eis
C 2 1
C T
Negative Positive Invalid
qGB Analyzer
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody Leishmania Ab LEISAB10 Device 1 Test device x 10/kit 24 M
GenBody Leptospira Ab LEPTAB10 Device 1 Test device x 10/kit 24 M
GenBody B. abortus Ab BABOAB10 Device 1 Test device x 10/kit 24 M
Middle East respiratory syndrome (MERS) is a viral respiratory disease caused by
a coronavirus (MERS-CoV) that was first identified in Saudi Arabia in 2012.A typical
case of MERS includes of fever, cough, and/or shortness of breath. Pneumonia is
a common finding on examination.
Gastrointestinal symptoms, including diarrhoea, have also been reported.
*(Previous page) Brucellosis in cattle is a disease caused by Brucella abortus (B.
abortus), a facultative, intracellular bacterium. The major mode of disease
transmission is ingestion of B. abortus organisms that may be present in tissues
of aborted fetuses, fetal membranes and uterine fluids. Abortion is the outstanding
clinical feature of the disease. If the carrier state develops in a majority of infected
cows in a herd, the clinical manifestations may be reduced milk production, dead
calves at term and a higher frequency of retained placentas.
Rapid Test for B. abortus Ab and MERS-CoV Ag
GenBody MERS-CoV Ag is a assay kit for MERS coronavirus antigens in sputum specimens from camel or human.
1. GenBody test device individually foil-pouched
with a desiccant
2. Assay solution in tube
3. Disposable dropper
4. Sterilized swab
5. Instruction manual for use
General Information
Material Provided
Ordering Information
GenBody MERS Ag
Specimen Nasal swab
Diagnostic target MERS CoV antigens
Sensitivity
Specificity
Analytical sensitivity 4x10 pfu/ml
MERS-CoV AgWorld First Product
To
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ME
RS
-Co
V A
g M
EM
ER
S-C
oV
Ag
ME
ME
RS
-Co
V A
g M
EEM
ER
S-C
oV
Ag
ME
ME
RS
-Co
VA
gM
E
C 2 1
C T
Negative
ME
RS
-Co
V A
g M
EM
ER
S-C
oV
Ag
ME
ME
RS
-Co
V A
g M
EEM
ER
S-C
oV
Ag
ME
ME
RS
-Co
VA
gM
E
C 2 1
C T
Positive
ME
RS
-Co
V A
g M
EM
ER
S-C
oV
Ag
ME
ME
RS
-Co
V A
g M
EEM
ER
S-C
oV
Ag
ME
ME
RS
-Co
VA
gM
E
C 2 1
C T
ME
RS
-Co
V A
g M
EM
ER
S-C
oV
Ag
ME
ME
RS
-Co
V A
g M
EEM
ER
S-C
oV
Ag
ME
ME
RS
-Co
VA
gM
E
C 2 1
C T
Invalid
GenBody MERS-CoV Ag
Specimen Take the solution
MERS-C
oV A
g M
ERS
MERS-C
oV A
g M
ER
MERS-C
oV A
g M
ERM
ER
MERS-C
oV A
g M
ER
MERS-C
oV A
g M
ER
C 2 1
C T
Load 3~4 drops ofsample solution
5~10minutes
ME
RS
-Co
V A
g M
ER
ME
RS
-Co
VA
gM
ER
ME
RS
-Co
V A
g M
ERR
ME
RS
-Co
VA
gM
ER
ME
RS
-Co
VA
gM
ER
C 2
1
C T
ReadingMix
6X
Test Procedure & Interpretation
Negative Positive Invalid
qGB Analyzer
Product Name Cat. No. Type Packing Unit Shelf Life
GenBody MERS-CoV Ag MERSAG10 Device 1 Test device x 10/kit 24 M
MERSAG20 Device 1 Test device x 20/kit 24 M
Gen
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Wound dressing device
The main protein components of the Extracellular Matrix (ECM) are collagen, elastin, and hyaluronic acid. The cells in the
wound are necessary to proliferate the base matrix. When the wound occurs, many proteases are secreted around the wound.
Wound healing needs rapid ECM (extracellular matrix) proliferation but the combination with main protein and proteases
makes the creation of ECM is slowly created.
There are a lot of proteases, bacteria, and dead cells around the wound area. Neo Skin Vet causes the osmotic pressure with
body fluids instantly then makes clean wound because of isolating substances that interfere with the wound healing. Herbal
extract in the Neo Skin Vet are caught proteases and bacteria and allow a wound to be rapidly healed. NDA(NSV) covers the
wound completely and degrades cycloxygenase then relieves pain instantly.
Neo Skin Vet (NSV)
Product function Adhesive transparent wound dressing prosthesis
Applications Surgical wound, bed sore, ulcer, burns
KFDA registration no. Medical device 11-504
KQIA registration no. Veterinary Medical device, No. 084-001
Product Name Cat. No. Type Packing Unit Shelf Life
Neo Skin Vet(Wound dressing)
NSV0010 Gel 1g x 5 ea/box 36 M
NSV0030 Gel 3g x 1 ea/box 36 M
NSV0050 Gel 5g x 1 ea/box 36 M
1. Before use, read carefully and understand well the manual.
2. Clean the wound area.
* To the clean wound: disinfect the area
* To the dirty wound: disinfect after removing the pus or body secretions
3. Apply 1 gram (g) of NSV onto the wound area.
* When use the pumping style of product, press slowly to pump.
* 1 g can cover 7 cm x 7 cm of the area.
4. Spread carefully the NSV using the sterilized swab (not provided).
1. Keep at room temperature
2. Before the applied product to be dry, you should avoid the water from the wound.
3. Do not inhale the contents consciously.
4. Do not use NSV to person who uses other external therapeutic agents for bed sore.
5. If container is damaged or validate is expired, do not use it.
* Storage : Room temperature, sealed & light protected
Procedure to use
Precautions
General Information
Ordering Information
To promote the wound healing, regeneration and pain relief at the
same time! Neo Skin Vet for animal use and Neo Dermal Activator
for human use.
The world first wound dressing prosthesis from natural ingredient.
New mechanism for fast wound healing and pain relief.
Neo Skin Vet(NSV)
World First Product
NanpSign Urine Strips are dip-and-read test strips for In Vitro Diagnostic
Use only for testing above items in urine. Test result may provide information
regarding the status of carbohydrate metabolism, kidney and liver function,
acid-base balance, and urinary tract infection. It is measured by comparison
of test paper attached to a plastic strip with the color chart blocks printed on
the vial label. The strips may be read visually. They can also be read
instrumentally, using urine chemistry analyzers.
Veterinary Urine Test
GenBody Urine Strip is for the rapid determination of Urobilinogen, Glucose, Bilirubin, Ketones (Acetoacetic Acid), Specific
Gravity, Blood, pH, Protein, Nitrite, Leukocytes and Ascorbic Acid in urine.
GenBody Urine Strip & Reader
Product Name Cat. No. Parameter Type Packing Unit Shelf Life
GenBody UriVET-10P
USVET10A Glu, Pro, pH, Blood, Ke, Bil, Uro, Nit, Specific, Gravity, Leu
Strip 50 strip/vial 24 M
USVET10B Strip 100 strip/vial 24 M
GenBody UriVET-11P
USVET11A Glu, Pro, pH, Blood, Ke, Bil, Uro, Nit, Specific, Gravity, Leu, As Acid
Strip 50 strip/vial 24 M
USVET11B Strip 100 strip/vial 24 M
General Information
Material Provided
Test Procedure
Ordering Information
Sensitivity
Occult Blood 10 RBC/
Bilirubin 0.5 mg/dL
Urobilinogen 2 mg/dL
Ketones 5 mg/dL
Protein 15 mg/dL
Glucose 100 mg/dL
Leukocyte 15-25 WBC/
Ascorbic acid 10 mg/dL
Urine Strip
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uVET AS720 AS300
Gen
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BS, Body Secretions; S, Serum; P, Plasma; WB, Whole Blood; Q, Quantitative
Group Product Name Cat. No. Description SpecimenPackage
(/Kit)
Shelf Life
(month)
Sensitivity
(%)
Speficifity
(%)
Analytical
SensitivityComments
Dogs
GenBody CPV Ag CPVAG010 Canine parvovirus antigen test Feces 1Tx20 24 99.9 99.0 10 HAU/ml
GenBody CCV Ag CCVAG010 Canine coronavirus antigen test Feces 1Tx20 24 99.0 98.5 4x103 TCID50/ml
GenBody CCV/CPV AgCCPAG010
Canine coronavirus/parvovirus antigen test Feces1Tx10
24 99.0/ 99.9 98.5/99.0 -CCPAG020 1Tx20
GenBody CDV AgCDVAG010
Canine distemper virus antigen test BS1Tx10
24 99.2 99.5 102.3 TCID50/mlCDVAG020 1Tx20
GenBody CIV Ag CIVAG010 Canine influenza virus antigen test BS 1Tx10 24 90.5 99.9 16 HAU/ml
GenBody CAV2 Ag CAV2AG10 Canine adenovirus 2 antigen test BS 1Tx10 24 97.0 98.0 1.2 s/CO
GenBody CDV Ag/CIV Ag combo CDIVAG10 Canine distemper virus antigen /
canine influenza virus antigen combo test BS 1Tx10 24 99.2/90.5 99.5/99.9 -
GenBody CDV Ag/CAV2 Ag combo CDAVAG10 Canine distemper virus antigen /
canine adenovirus 2 antigen combo test BS 1Tx10 24 99.2/97.0 99.5/98.0 -
GenBody CHW AgCHWAG010
Canine heartworm antigen test S/P/WB1Tx10
24 95.0 99.0 5 ng/mlCHWAG020 1Tx20
GenBody B.canis Ab BCAAB010 Canine Brucella (B. canis) antibody test S/P/WB 1Tx10 24 98.0 99.9 -
GenBody E.canis Ab ECAAB010 Canine Ehrlichia (E. canis) antibody test S/P/WB 1Tx10 24 98.0 99.8 -
GenBody Canine IgECNIGE010
Canine total IgE test S/P1Tx10
24 98.0 98.5 -CNIGE020 1Tx20
GenBody CPV Ab CPVAB010 Canine parvovirus antibody test S/P 1Tx10 24 Q Q 1:10 HI
GenBody CDV Ab CDVAB010 Canine distemper virus antibody test S/P 1Tx10 24 Q Q 1:16 NA
GenBody CPV/CDV Ab CPDAB010 Canine CPV/CDV antibody combo test S/P 1Tx10 24 Q Q -
Cats
GenBody FPV Ag FPVAG010 Feline parvovirus antigen test Feces 1Tx10 24 98.0 99.5 10 HAU/ml
GenBody FCoV Ag FCOAG010 Feline corona virus antigen test Feces 1Tx10 24 96.0 99.0 5x103 TCID50/ml
GenBody FHV Ag FHVAG010 Feline herpes virus antigen test B/S 1Tx10 24 98.0 99.5 -
GenBody FHV Ag/Ab FHVGB010 Feline herpes virus antigen / antibody test B/S 1Tx10 24 98.0/99.0 99.5/99.5 -
GenBody FIV Ab FIVAB010 Feline immunodeficiency virus antibody test S/P/WB 1Tx10 24 99.5 99.9 1.5 s/CO
GenBody FIV Ag/Ab combo FIVAGB10 Feline immunodeficiency virus antigen / antibody combo test S/P/WB 1Tx10 24 95.0/99.5 99.9/99.9 5 ng/ml for Ag
1.5 s/CO for Ab
GenBody FeLV Ag FELAG010 Feline leukemia virus antigen test S/P/WB 1Tx10 24 95.2 98.0 2 ng/ml
GenBody FeLV Ag/FIV Ab combo FELFIV10 Feline immunodeficiency virus antibody /
leukemia virus antigen combo test S/P/WB 1Tx10 24 95.2/99.5 98.0/99.9 2 ng/ml for FeLV 1.5 s/CO for FIV
WORLD BEST RAPID TEST FOR SMALL PETS
World Best
World Best
World Best
World First
World First
World First
World First
World First
To
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co
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an
y to
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Group Product Name Cat. No. Description SpecimenPackage
(/Kit)
Shelf Life
(month)
Sensitivity
(%)
Speficifity
(%)
Analytical
SensitivityComments
Cats
&
Dogs
GenBody Giardia Ag GIAAG010 Giarida antigen test Feces 1Tx10 24 - 99.0 100~200 cysts/100ml
GenBody Tg Ab TGAB0010 Toxoplasma gondii antibody test S/P/WB 1Tx10 24 99.9 99.0 0.8 s/CO
GenBody Tg IgM/IgG 4.0 TGMG4010 Toxoplasma canine IgM/feline IgM / total IgG combo test S/P/WB 1Tx10 24 98.0/98.0/99.0 99.0/99.0/99.9 1.0/1.0/0.8 s/CO
GenBody Leishmania Ab LEISAB10 Leishmania antibody test S/P/WB 1Tx10 24 99.5 99.6 1.2 s/CO
GenBody Leptospira Ab LEPTAB10 Leptospira antibody test S/P/WB 1Tx10 24 99.6 99.8 1.1 s/CO
GenBody cTnI CTNI0010 Small animal cardiac troponin I test S/P/WB 1Tx10 24 Q Q 0.5 ng/ml
GenBody D-Dimer DDIM0010 Small animal d-dimer test S/P/WB 1Tx10 24 Q Q 100 ng/ml
GenBody cTnI/D-dimer Combo TNIDDM10 Small animal cardiac troponin I /
D-dimer combo test S/P/WB 1Tx10 24 Q Q 0.5 ng/ml / 100 ng/ml
GenBody cTnI/BNP Combo TNIBNP10 Small animal cardiac troponin I /
BNP combo test S/P/WB 1Tx10 24 Q Q 0.5 ng/ml / 0.1 ng/ml
GenBody Rota AgROTAG010
Rotavirus antigen test Feces1Tx10
24 99.0 98.5 103.5 TCIDTCID50/ml
ROTAG020 1Tx20
Others
GenBody B.abortus Ab BABOAB10 Bovine Brucella (B. abortus) antibody test S/P/WB 1Tx10 24 99.5 99.8 1.0 s/CO
GenBody MERS-CoV Ag MERSAG10 Middle East Respiratory Syndrome (MERS) corona virus antigen test
Nasal Swab 1Tx10 24 - - 4 x 10 pfu/ml
RDT
MachineGenBody qGB Analyzer QGB0010 Quantitative analyzing machine for GenBody veterinary
rapid diagnostic test 1 Unit -
Urine
strip
&
Analyzer
GenBody UriVET-10PUSVET10A Urobilinogen, Glucose, Bilirubin, Ketone,
Specific Gravity, Blood, pH, Protein, Nitrite, Leukocyte
Urine50T/Kit
24 Q QNote the insert
USVET10B 100T/Kit Note the insert
GenBody UriVET-11PUSVET11A Urobilinogen, Glucose, Bilirubin, Ketone,
Specific Gravity, Blood, pH, Protein, Creatinine, Nitrite, Leukocyte
Urine50T/Kit
24 Q QNote the insert
USVET11B 100T/Kit Note the insert
GenBody Uri-BHB (Milk) USBHB10 -Hydroxybutyrate (BHB Milk) Milk 50T/Kit 24 Q Q
GenBody Uri-LDH (Milk) USLDH10 Lactate Dehydrogenase (LDH Milk) Milk 50T/Kit 24 Q Q
GenBody uVET Analyzer UVET010 45 Tests(Max 120 Tests)/Hour, LCD Touch Screen, No Built-in Printer, PC user software 1 Unit -
GenBody mCOW Analyzer MCOW010 45 Tests(Max 120 Tests)/Hour, LCD Touch Screen, No Built-in Printer, PC user software 1 Unit -
External Printer UGBEP10 External printer for EXCLUSIVE use with uVET Analyzer or mCOW Analyzer 1 Unit -
Medical
deviceNeo Skin Vet
NSV0010
Medical device for fast wound healing & pain relief
1g
36 -NSV0030 3g
NSV0050 5g
World First
World First
World First