CYFIP2抗体 [N2C1], Internal

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.

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 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data are based on Human Protein Atlas program.

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.

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.