Answer:It recognizes guinea pig IgG heavy and light chains rather than a specific cellular antigen.
Answer:Horseradish peroxidase produces a detectable signal with a compatible colorimetric or chemiluminescent substrate.
Answer:Cross-adsorption reduces unwanted binding to immunoglobulins from several other species and helps limit background staining.
Abcam Goat Anti-Guinea Pig IgG H&L-HRP Preadsorbed Secondary Antibody enables enzymatic detection of guinea pig primary antibodies in immunoassays. The polyclonal goat antibody recognizes guinea pig immunoglobulin heavy and light chains and carries horseradish peroxidase for colorimetric or chemiluminescent substrate reactions. Preadsorption against several other animal immunoglobulins reduces cross-species background when samples contain mixed antibody components. Suitable research applications include western blotting, ELISA, immunocytochemistry and paraffin-section immunohistochemistry. The 500 µg presentation provides liquid antibody for dilution into a validated assay buffer. Determine the working concentration from the detection platform, membrane or specimen type and expected antigen abundance rather than using a single dilution for every experiment. Block nonspecific binding sites and wash thoroughly between incubations to preserve signal specificity. Select the HRP substrate and development interval to maintain a useful dynamic range. This reagent detects guinea pig immunoglobulins and is not a primary antibody against a specific cellular antigen.
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