Formalin-fixed and paraffin-embedded human Lymph reacted with IGHA1 Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Western blot of IGHA1 antibody in CEM cell line lysates (35 ug/lane). IGHA1 (arrow) was detected using the purified antibody.
Flow cytometric of CEM cells using IGHA1 Antibody (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.