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 a conserved C-terminal SH2 domain

and studies in mice show that overexpression of this gene may be relevant to the pathogenesis of Alzheimer disease

and sterile packaging to ensure purity and accuracy

as well as in the testicular and epididymal spermatozoa suggesting an important role in late spermatogenesis

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.