Invitrogen™ Goat anti-Syrian Hamster IgG (H+L) Secondary Antibody, FITC, eBioscience™

Description

Description: This antibody reacts with the heavy chains on Syrian hamster IgG and with light chains common to most Syrian hamster immunoglobulins. Reactions to non-immunoglobulin hamster proteins have not been detected. Applications Reported: This polyclonal antibody can be used for detection of purified Syrian hamster immunoglobulins (IgG) in flow cytometry. At high concentrations, cross-reaction to Armenian hamster IgG has been observed. Applications Tested: FITC Anti-Syrian Hamster IgG has been tested by flow cytometric analysis to detect purified Syrian hamster monoclonal antibodies. This can be used at less than or equal to 0.5 μg per test. A test is defined as the amount (μg) of antibody that will stain a cell sample in a final volume of 100 μL. Cell number should be determined empirically but can range from 10^5 to 10^8 cells/test. It is recommended that the antibody be carefully titrated for optimal performance in the assay of interest. In addition, it has been adsorbed and tested by ELISA to ensure minimal cross reaction to human, bovine, horse, rabbit, rat, and mouse serum proteins, but may cross-react with immunoglobμLins from other species. Excitation: 488 nm; Emission: 520 nm; Laser: Blue Laser. Filtration: 0.2 μm post-manufacturing filtered.

Anti-Hamster secondary antibodies are affinity-purified antibodies with well-characterized specificity for hamster immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.