SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series also known as AIFM3 (apoptosis-inducing

also known as AIFM3 (apoptosis-inducing factor

Defects in this gene are the cause of LIG4 syndrome

|mass spectrometry: PubMed:10233762|online information:CXCL11 entry|Belongs to the intercrine alpha (chemokine CxC) family

This gene is widely expressed in many tissues

Mutations in this gene are associated with the growth of certain tumors

SIL1 Rabbit Polyclonal Antibody, 100ul PCR Series also known as AIFM3 (apoptosis-inducingThis gene encodes a resident endoplasmic reticulum (ER) N linked glycoprotein with an N terminal ER targeting sequence 2 putative N glycosylation sites and a C terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco Sjogren syndrome. Alternate transcriptional splice variants have been characterized.