CLH2 Rabbit Polyclonal Antibody, 50ul ssDNA Synthesis ensuring the highest level of

ensuring the highest level of accuracy and purity

Pseudogenes of this gene are present on chromosomes 4 and 17

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Defects in CLDN19 are the cause of hypomagnesemia renal with ocular involvement (HOMGO)

CLH2 Rabbit Polyclonal Antibody, 50ul ssDNA Synthesis ensuring the highest level ofThis gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma DiGeorge syndrome and velo cardio facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene.