Anti-HTLV Type I gp46 Clone 67/5.5.13.1 (100 µg)

Determine the presence of Human T-Lymphotropic Virus (HTLV) Type I protein

This murine monoclonal antibody reacts with Human T-Lymphotropic Virus Type I (HTLV-I) surface protein, gp46. The antibody was raised by immunizing BALB/c mice with purified HTLV-I lysate. The epitope is located between amino acids 210-306 of the viral env gene. Cross-reactivity with the surface protein of HTLV-II (MoT) has been observed. The antibody is of the IgG1 subclass and has been purified from serum-free culture supernatant by concentration and ammonium sulfate precipitation. The antibody is greater than 85% pure as determined using SDS polyacrylamide gel electrophoresis. Anti-HTLV-I gp46 Clone 67/5.5.13.1 exhibits reactivity with viral lysates using solid-phase enzyme immunoassay and immunoblotting. It also reacts with HTLV-I infected cell lines using indirect immunofluorescence. The antibody immunoprecipitates gp46 surface protein from radiolabeled cell lysates, as well as viral precursor protein.

The antibody is used to detect HTLV-I surface protein and its precursor in lysates prepared from virions or infected cells. Using immunoblotting and/or radioimmunoprecipitation analysis, the biosynthesis and metabolism of viral surface protein may be studied. Antibody dilutions should be prepared using buffers containing suitable protein in order to stabilize antibody activity. Optimal dilution of antibody must be determined experimentally by the investigator.

What's included: One 100 µg vial of Anti-HTLV-I gp46 (clone 67/5.5.13.1) in phosphate-buffered saline (PBS). Supplier Certificate of Analysis (CoA) is included with product shipment.

• 100 µg vial of Anti-HTLV-I gp46 (clone 67/5.5.13.1)

• Antibody in phosphate-buffered saline (PBS) matrix

• Store at -10°C or below

The antibody is used to detect HTLV-I surface protein and its precursor in lysates prepared from virions or infected cells. Using immunoblotting and/or radioimmunoprecipitation analysis, the biosynthesis and metabolism of viral surface protein may be studied. Antibody dilutions should be prepared using buffers containing suitable protein in order to stabilize antibody activity. Optimal dilution of antibody must be determined experimentally by the investigator.

• ENGLISH (PI)
• ENGLISH (SDS)

These products are supplied for research purposes only. It is not intended for use in the diagnosis or prognosis of disease, or for screening and may not be used as a confirmatory test in diagnostic situations. Propagation or commercialization are prohibited without prior written consent from Antylia Scientific.

The suitability and performance characteristics should be determined by your laboratory for each intended usage.