PRPF39 Polyclonal Antibody, 20ul Metabolic enzymes Defects in CLDN19 are the

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

The expression of ADH7 is much more abundant in stomach than liver

Specifically binds to the 5-TCAT-3 DNA sequence (By similarity)

Interleukin-31 receptor subunit alpha encoded by IL31RA belongs to the type I cytokine receptor family

Made with durable and sterile PP material

PRPF39 Polyclonal Antibody, 20ul Metabolic enzymes Defects in CLDN19 are thePRPF39 also termed as Pre mRNA processing factor 39 or PRP39 homolog is a 669 amino acid protein, which contains 7 HAT repeats and belongs to the PRP39 family. PRPF39 localizes in nucleus and may play a role in mRNA splicing.