SHRM3 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Defects in this gene could

Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

and sterile packaging to ensure purity and accuracy

Three alternatively spliced transcript variants encoding different isoforms have been found for this gene

Activates the Arp2/3 complex to induce branched actin filament networks

and a conserved C-terminal SH2 domain

SHRM3 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Defects in this gene couldThis gene encodes a PDZ domain containing protein that belongs to a family of Shroom related proteins. This protein may be involved in regulating cell shape in certain tissues. A similar protein in mice is required for proper neurulation.