Untreated (–) and treated (+) A431 whole cell extract (30 μg) were separated by 5% SDS-PAGE, and the membranes were blotted with EGFR (phospho Tyr1086) antibody [HL3284] (GTX640938) diluted at 1:200000 and competitor's antibody (Highly Cited Competitor) diluted at 1:200000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

*The competitor is not affiliated with GeneTex and does not endorse this product.

EGFR (phospho Tyr1086) antibody [HL3284] detects EGFR (phospho Tyr1086) protein by immunofluorescent analysis.
Sample: Mock and treated A431 cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: EGFR (phospho Tyr1086) stained by EGFR (phospho Tyr1086) antibody [HL3284] (GTX640938) diluted at 1:500.
Blue: Fluoroshield with DAPI (GTX30920).

Specificity test was performed by coating the plate with EGFR peptide and EGFR (phospho Tyr1086) peptide (15.63 ng/mL). Coated peptides were probed with EGFR (phospho Tyr1086) antibody [HL3284] (GTX640938) (1 μg/mL). Goat anti-rabbit IgG antibody (HRP) (GTX213110-01) (1:10000) was used to detect the bound primary antibody.