abinScience secondary antibodies are optimized for Western blot, IHC/IF, ELISA and flow cytometry. Choose cross-adsorbed and highly cross-adsorbed specificities to minimize species cross-reactivity, Fc-specific or H+L binding for assay needs, and F(ab')2 fragments for FcR-rich tissues. Conjugates include HRP/AP, Alexa Fluor 488/555/594/647, FITC, PE, APC and biotin. Each lot provides recommended dilutions, application images and CoA for consistent performance. RUO
H+L recognizes both heavy and light chains for robust detection; Fc-specific avoids light-chain cross-reactivity (e.g., when multiple primaries share light chains) and reduces background in certain assays.
Use F(ab')2 in IHC/IF when Fc receptor–bearing cells (e.g., macrophages) cause background, or when better tissue penetration is desired.
Secondary antibodies are adsorbed against serum proteins from non-target species to minimize cross-reactivity; “highly cross-adsorbed” further reduces off-target binding in multi-species samples.
Match lasers/filters (e.g., AF488 for 488 nm, AF647 for 633–640 nm); consider dye brightness and panel spillover to maintain resolution.
Yes—include a no-primary/secondary-only control to assess non-specific binding and set gates/background.
All antibodies are for Research Use Only and not for diagnostic procedures.

ELISA
Goat
IgG
HRP
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