HSP10 Polyclonal Antibody, 50ul Nucleic Acid Amplification Mutations affecting this gene are

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIG

Inhibition of inositol monophosphate hydroylosis and subsequent depletion of inositol for phosphatidylinositol synthesis may explain the anti-manic and anti-depressive effects of lithium administered to treat bipolar disorder

The protein encoded by this gene is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor and a member of the GDNF receptor family

Once inside the cell

HSP10 Polyclonal Antibody, 50ul Nucleic Acid Amplification Mutations affecting this gene areHSPE1 encodes a major heat shock protein which functions as a chaperonin. Its structure consists of a heptameric ring which binds to another heat shock protein in order to form a symmetric, functional heterodimer which enhances protein folding in an ATP dependent manner. This gene and its co chaperonin, HSPD1, are arranged in a head to head orientation on chromosome 2. Naturally occurring read through transcription occurs between this locus and the