NDUA5 Polyclonal Antibody, 50ul Insect Expression Defects in CLDN19 are the

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

Defects in this gene are the cause of selective C1s deficiency

induction:Upon B-cell activation

The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity

while its DNase/RNase-free and pyrogen-free properties provide peace of mind

NDUA5 Polyclonal Antibody, 50ul Insect Expression Defects in CLDN19 are theThis nuclear gene encodes a conserved protein that comprises the B13 subunit of complex I of the mitochondrial respiratory chain. The encoded protein localizes to the inner mitochondrial membrane, where it is thought to aid in the transfer of electrons from NADH to ubiquinone. Alternative splicing results in multiple transcript variants. There are numerous pseudogenes of this gene on chromosomes 1, 3, 6, 8, 9, 11, 12, and 16.