Item-specific tested applications, recommended dilutions, incubation times, and positive controls are not specified for Ab219251; refer to the CoA/Spec Sheet. The following are general, literature-based starting points for HRP-conjugated anti-GAPDH antibodies and should be optimized by the user:
- Western blot (general):
- Sample: denatured whole-cell lysates (10–30 µg/lane).
- Membrane: PVDF or nitrocellulose; block 1 h in 5% milk/BSA in TBS-T.
- Antibody incubation: HRP-conjugated primary 1 h RT or overnight 4°C in blocking buffer; wash 3–5× with TBS-T.
- Detection: chemiluminescent HRP substrate; image within minutes of development.
- ELISA (general):
- Coat plates with antigen or capture antibody, block with protein blocker, incubate with HRP-conjugated antibody, develop with TMB, stop with acid, read at 450 nm.
- IHC/ICC (general):
- Fix with PFA; optional antigen retrieval; block endogenous peroxidase with H2O2 (if chromogenic); incubate with HRP-conjugated antibody; develop with DAB; counterstain.
Controls (general): Include no-primary and isotype controls; verify band at ~36–38 kDa (GAPDH) in WB.
Note: Avoid azide in detection steps due to HRP inhibition. These guidelines are not product-specific instructions.