Sar1B Polyclonal Antibody, 100ul 3D Culture Mutations in this gene have

Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis

The Y-linked genes arose by retrotransposition of an mRNA from this gene

laminin receptor 1

some of which may result in the formation of fusion proteins

ABCC13 is a member of the superfamily of genes encoding ATP-binding cassette (ABC) transporters

Sar1B Polyclonal Antibody, 100ul 3D Culture Mutations in this gene haveThe protein encoded by SAR1B (secretion associated Ras related GTPase 1B) is a small GTPase that acts as a homodimer. The encoded protein is activated by the guanine nucleotide exchange factor PREB and is involved in protein transport from the endoplasmic reticulum to the Golgi. This protein is part of the COPII coat complex. Defects in SAR1B are a cause of chylomicron retention disease (CMRD), also known as Anderson disease (ANDD). Two transcript