phospho-MLKL (S358) mouse Monoclonal Antibody(6B4), 50ul Syringe Filter Mutations in this gene cause

Mutations in this gene cause congenital heart defects| multiple types| 2 (CHTD2)

The protein encoded by this gene is localized to the nucleus and cytoplasm of fetal germ cells and to the cytoplasm of developing oocytes

VIM (vimentin) encodes a member of the intermediate filament family

This gene encodes a member of the 17beta-hydroxysteroid dehydrogenase family of short-chain dehydrogenases/reductases

• Adjustable rotational mixing speed

phospho-MLKL (S358) mouse Monoclonal Antibody(6B4), 50ul Syringe Filter Mutations in this gene causeThis gene belongs to the protein kinase superfamily. The encoded protein contains a protein kinase like domain however, is thought to be inactive because it lacks several residues required for activity. This protein plays a critical role in tumor necrosis factor (TNF) induced necroptosis, a programmed cell death process, via interaction with receptor interacting protein 3 (RIP3), which is a key signaling molecule in necroptosis pathway. Inhibitor