SSA27 Polyclonal Antibody, 50ul Measuring Instruments Disruption of this gene is

Disruption of this gene is associated with focal epilepsy and speech disorder with or without mental retardation

This gene encodes an integral membrane protein which is classified as a member of the metalloproteinase family

Homotetramers consisting of the intact protein| or type C subunit| exhibit high affinity for heparin and are anchored to the ECM

and overexpression of this gene in primary tumors is linked to the repression of let-7 family of microRNAs and derepression of let-7 targets

and mediate the signal transduction from various receptors of the TNFR superfamily

SSA27 Polyclonal Antibody, 50ul Measuring Instruments Disruption of this gene isThis antigen is recognized by a subset of anti centromere antibodies from patients with scleroderma and or Sjogren's syndrome. Subcellular localization has not yet been established.