Background

Enables several functions, including phosphatidylinositol-3,4,5-trisphosphate binding activity; protein serine/threonine kinase binding activity; and type I transforming growth factor beta receptor binding activity. Involved in several processes, including cell surface receptor signaling pathway; positive regulation of cellular component biogenesis; and positive regulation of intracellular signal transduction. Acts upstream of or within cell adhesion and protein localization to cell junction. Located in several cellular components, including adherens junction; cytoplasmic side of plasma membrane; and focal adhesion. Biomarker of acute myeloid leukemia.

Images

	Western blotting analysis using anti-FERMT2 antibody (Cat#71114). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-FERMT2 antibody (Cat#71114, 1:5,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
	Western blotting analysis using anti-FERMT2 antibody (Cat#71114). FERMT2 expression in wild type (WT) and FERMT2 knockout (KO) HSHC cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-FERMT2 antibody (Cat#71114, 1:5,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
	Flow cytometric analysis of FERMT2 expression in HepG2 cells using anti-FERMT2 antibody (Cat#71114, 1:2,000). Green, isotype control; red, FERMT2.
	Immunocytochemical staining of HepG2 cells with anti-FERMT2 antibody (Cat#71114, 1:1,000). Nuclei were stained blue with DAPI; FERMT2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Low. Scale bar, 20 μm.