ITB8 Polyclonal Antibody, 50ul sgRNA Oligos Defects in this gene could

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

Human natural killer (NK) cells and activated lymphocytes express and store a distinct subset of neutral serine proteases together with proteoglycans and other immune effector molecules in large cytoplasmic granules

Alternatively spliced transcript variants have been found for STAT5A

is involved in controlling a diverse set of essential cellular functions

ITB8 Polyclonal Antibody, 50ul sgRNA Oligos Defects in this gene couldThis gene is a member of the integrin beta chain family and encodes a single pass type I membrane protein with a VWFA domain and four cysteine rich repeats. This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex. In general, integrin complexes mediate cell cell and cell extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation. Alternatively spliced variants which