Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with CYFIP2 antibody [N2C1], Internal (GTX110897) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with CYFIP2 antibody [N2C1], Internal (GTX110897) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with CYFIP2 antibody [N2C1], Internal (GTX110897) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.

CYFIP2 antibody [N2C1], Internal detects CYFIP2 protein at cytoplasm and nucleus by immunohistochemical analysis.
Sample: Paraffin-embedded mouse duodenum.
CYFIP2 stained by CYFIP2 antibody [N2C1], Internal (GTX110897) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with CYFIP2 antibody [N2C1], Internal (GTX110897) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.