CLCN1 Polyclonal Antibody, 20ul Drying & Desiccation and is necessary for the

and is necessary for the expression of glucose transporter

Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID)| in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins| whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia

and is induced by transforming growth factor-beta (TGF-beta) to repress TGF-beta receptor II gene expression

This gene encodes a protein that is a member of the dickkopf family

Has narrower substrate selectivity compared to SLC7A5 and SLC7A8 and mainly transports branched-chain amino acids and phenylalanine

CLCN1 Polyclonal Antibody, 20ul Drying & Desiccation and is necessary for theThe CLCN family of voltage dependent chloride channel genes comprises nine members (CLCN1 7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant