Hcv Recombinant Antigen

INTENDED USE

The HCV Gold Rapid Screen Test (RST) is a Chromatographic immunoassay (CIA) for direct qualitative detection of antibodies to

Hepatitis C type virus (HCV) in human serum/ plasma and whole blood.

PRINCIPLE

HCV RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HCV in human serum/plasma and whole blood. HCV recombinant antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HCV recombinant antigens. If antibodies to HCV present, a pink colored band will develop on the membrane in proportion to the amount of HCV antibodies present in the specimen .Absence of this pink colored band in the test region suggests a negative result. To serve as a procedural control, a purple colored band in the control region will always appear regardless the presence of antibodies to HCV.

REAGENTS AND MATERIALS PROVIDED

1. One pouched cassette with desiccant.

2. Blood diluent in a dropper bottle, stored at 4-30°C.

3. One piece of operating instruction.

WARNING AND PRECAUTIONS

1. For in vitro diagnostic uses only.

2. All patient samples should be treated as if capable of transmitting diseases.

3. Do not interchange reagents from different lots or use test kit beyond expiration date.

4. Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.

STORAGE

The kits should be stored at temperature 4-30°C, the sealed pouch for the duration of the shelf life (24 months).

INTENDED USE

The HCV Gold Rapid Screen Test (RST) is a Chromatographic immunoassay (CIA) for direct qualitative detection of antibodies to

Hepatitis C type virus (HCV) in human serum/ plasma and whole blood.

PRINCIPLE

HCV RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HCV in human serum/plasma and whole blood. HCV recombinant antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HCV recombinant antigens. If antibodies to HCV present, a pink colored band will develop on the membrane in proportion to the amount of HCV antibodies present in the specimen .Absence of this pink colored band in the test region suggests a negative result. To serve as a procedural control, a purple colored band in the control region will always appear regardless the presence of antibodies to HCV.

REAGENTS AND MATERIALS PROVIDED

1. One pouched cassette with desiccant.

2. Blood diluent in a dropper bottle, stored at 4-30°C.

3. One piece of operating instruction.

WARNING AND PRECAUTIONS

1. For in vitro diagnostic uses only.

2. All patient samples should be treated as if capable of transmitting diseases.

3. Do not interchange reagents from different lots or use test kit beyond expiration date.

4. Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.

STORAGE

The kits should be stored at temperature 4-30°C, the sealed pouch for the duration of the shelf life (24 months).

INTENDED USE

The HCV Gold Rapid Screen Test (RST) is a Chromatographic immunoassay (CIA) for direct qualitative detection of antibodies to

Hepatitis C type virus (HCV) in human serum/ plasma and whole blood.

PRINCIPLE

HCV RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HCV in human serum/plasma and whole blood. HCV recombinant antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HCV recombinant antigens. If antibodies to HCV present, a pink colored band will develop on the membrane in proportion to the amount of HCV antibodies present in the specimen .Absence of this pink colored band in the test region suggests a negative result. To serve as a procedural control, a purple colored band in the control region will always appear regardless the presence of antibodies to HCV.

REAGENTS AND MATERIALS PROVIDED

1. One pouched cassette with desiccant.

2. Blood diluent in a dropper bottle, stored at 4-30°C.

3. One piece of operating instruction.

WARNING AND PRECAUTIONS

1. For in vitro diagnostic uses only.

2. All patient samples should be treated as if capable of transmitting diseases.

3. Do not interchange reagents from different lots or use test kit beyond expiration date.

4. Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.

STORAGE

The kits should be stored at temperature 4-30°C, the sealed pouch for the duration of the shelf life (24 months).

Product Details:

Number of Reactions(Preps)/Kit 96 Wells
Brand CTK BioTech
Sample serum or plasma
Storage 2 - 8 C
Cat No : AE0510
INTENDED USE:
The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of IgG to Hepatitis C virus (HCV) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HCV. Any reactive specimen with the TRUSTwell HCV IgG ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.

TEST PRINCIPLE:

The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the indirect EIA technique for the detection of the IgG to HCV in human serum or plasma. The TRUSTwell HCV IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with recombinant HCV antigens; 2) Liquid conjugates composed of mouse anti-human IgG conjugated with horse radish peroxidase (HRP-anti Human IgG conjugates). During the assay, the test specimen is first incubated with the coated microwells. The IgG anti HCV, if present in the specimen, bind to the antigens coated on the microwell surface. In the second incubation with the HRP-anti-human IgG conjugates, the IgG antibodies absorbed on the surface of microwell react to the HRP-anti-human IgG conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.

Clinical Performance:

A total of 1108 patient specimens from susceptible subjects were tested by the TRUSTwell HCV IgG ELISA Kit.

Relative Sensitivity:100%,
Relative Specificity:99.81%,
Overall Agreement:99.82%.

HIV Antigen/antibody for ELISA

recombinant antigen
HIV-1 gp41+gp120
HIV-1 gp41
HIV-2 gp36
HIV-1+2 gp41+gp120+gp36
HIV-1 P24
HIV-1 gp41+gp120-HRP conjugate
HIV-2 gp36-HRP conjugate

antibody
Monoclonal Anti-HIV P24
Polyclonal Anti-HIV P24 Biotin

HIV Antigen/antibody for Rapid test

recombinant antigen
HIV-1 gp41+120
HIV-2 gp36
HIV-1+2 gp41+36+120

antibody
Monoclonal Anti-HIV P24
Polyclonal Anti-HIV P24


Fapon Biotech provide gene engineering recombinant antigens and antibodys of HIV type 1¿¬¿«2 and group O, which can be used in ELISA and Rapid Test Kit, with high sensitive specific and stability.

General Information
One-Step HCV Rapid Test is to detect the antibodies to HCV in human serum, plasma or whole blood.
Applied highly purified recombinant proteins : Core,NS3,NS4,NS5
Method; Double Antigens Sandwich Method, the 4th generation Rapid Tests
Sensitivity : 100%, Specificity : 100%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min.

Viral Transport Kit

Innolab200600002PS-Semi-Auto Biochemistry Analyzer