Enzyme immunoassay for the detection of antibodies against Human
Hepatitis Virus Type C (HCV) RUO
Hepatitis C virus (HCV), which was formerly described as the
parenterally transmitted form of non-A, non-B hepatitis (NANBH)1, becomes a chronic disease in 50% of the cases.2 HCV can also be transmitted through intravenous drug abuse, and
household contact.3 Hepatitis C virus is a single stranded RNA virus with some
structural relations to the flavivirus family. Nucleic acid
sequences of HCV cDNA clones provided the basis for the
construction of recombinant peptides representing putative
hepatitis C virus proteins.4,5 Anti-hepatitis C virus antibody screening of blood using synthetic
or recombinant proteins, helped to identify apparently healthy
blood donors with anti-HCV antibodies who otherwise might have
transmitted the virus.6
This is an enzyme linked immunosorbent assay using recombinant
proteins derived from core regions of HCV virus to detect the
presence of HCV antibodies in human sera.
Materials provided with the kits:
Item
Description
96T
480T
1
Coating Plate
1
5
2
Negative Control
1ml
5ml
3
Positive Control
1ml
5ml
4
Sample Diluent
12ml
60ml
5
Enzyme Conjugate
12ml
60ml
6
Wash Buffer Concentrate (20x)
30ml
150ml
7
Substrate Solution A
6ml
30ml
8
Substrate Solution B
6ml
30ml
9
Stop Solution
6ml
30ml
10
Plastic Bag
1
5
11
Seal Paper
3
15
12
Manual
1 copy
5 copy
ASSAY PROCEDURE
It is strongly advised to analyze each specimen and controls in
duplicate. All the reagents should equilibrate to room temperature
before use.
Dispense 100ml(or 3 drops) of specimen diluent into individual test
wells.
Dispense 100ml positive control and negative control duplicate into
individual wells.
Add 10ml of each test sample into duplicate test wells; vortex to
mix.
Incubate for 30 minutes at 37°C
Wash each well 5 times by filling each well with diluted wash
buffer, then inverting the plate vigorously to get all water out
and blocking the rim of wells on absorbent paper for a few seconds.
Add 100ml of Enzyme Conjugate to each well. Mix it gently by
swirling the microtiter plate on flat bench for 1 minutes. Do not add Enzyme Conjugate to the blank well.
Incubate for 20 minutes at 37°C
Wash the plate 5 times as step 5.
Add one drop (50ml) of Substrate Solution A (HRP-substrate) to each
well, then add one drop (50ml) of Substrate Solution B (TMB) to
each well. Mix gently and incubate at 37°C for 10 minutes. .
Add one drop (50ml) of Stop Solution to each well to stop the color
reaction. Read the OD value at 450 nm/630 nm with dual filter plate
reader. It is option to read the OD value at 450 nm with single
filter plate reader. (using the OD value of the blank well to
correct all the OD reading from all wells)
Company Profile
Biovantion Inc is independent from international department of
Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro
diagnostic reagents manufacturer engaged in the research,
development, production, and focus on clinical testing for
infectious diseases, such as Hepatitis virus, Noro virus, Parvo
virus test kits, our products include rapid test cassette and Elisa
kits.
All our products have been registered in National Medical Products
Administration of China, in year 2020 we get Certificate of ISO
13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from
SGS. More importantly, we have awarded the registration certificate
from National Medical Products Administration for Diagnostic Kit
for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during
the outbreak in China, and also we developed COVID-19 Antigen test
; Neutralizing Antibody Test, these products selling well all
overthe world