B3GT6 Polyclonal Antibody, 20ul Fluorescent Staining Diseases associated with C1R include

Diseases associated with C1R include immunodeficiency due to an early component of complement deficiency and c1r/c1s deficiency

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The protein encoded by this gene forms a tetrameric cation channel that is permeable to calcium| sodium| and potassium and is regulated by free intracellular ADP-ribose

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases

B3GT6 Polyclonal Antibody, 20ul Fluorescent Staining Diseases associated with C1R includeThe enzyme encoded by this intronless gene is a beta 1,3 galactosyltransferase found in the medial Golgi apparatus, where it catalyzes the transfer of galactose from UDP galactose to substrates containing a terminal beta linked galactose moiety. The encoded enzyme has a particular affinity for galactose beta 1,4 xylose found in the linker region of glycosamines. This enzyme is required for glycosaminoglycan synthesis.