FCG3A Polyclonal Antibody, 50ul Microplate Mixer Mutations in SMC1A result in

Mutations in SMC1A result in Cornelia de Lange syndrome

Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist: one composed of multiple subunits| the other| a single subunit

This gene encodes a member of the lysophosphatidic acid receptor family

Receptor for eicosanoids and polyunsaturated fatty acids such as 5-oxo-6E

This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination

FCG3A Polyclonal Antibody, 50ul Microplate Mixer Mutations in SMC1A result inThis gene encodes a receptor for the Fc portion of immunoglobulin G, and it is involved in the removal of antigen antibody complexes from the circulation, as well as other other antibody dependent responses. This gene (FCGR3A) is highly similar to another nearby gene (FCGR3B) located on chromosome 1. The receptor encoded by this gene is expressed on natural killer (NK) cells as an integral membrane glycoprotein anchored through a transmembrane