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AR (Acetyl Lys632) Rabbit Polyclonal Antibody, 50ul Recombinant Ab Production Heterozygous loss-of-function mutations in KLF1

SKU: 63872142209

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AR (Acetyl Lys632) Rabbit Polyclonal Antibody, 50ul Recombinant Ab Production Heterozygous loss-of-function mutations in KLF1disease: Defects in AR are the cause of androgen insensitivity syndrome (AIS)

Store: aashay.com.au · Domain: aashay.com.au

Description

Heterozygous loss-of-function mutations in KLF1 result in the dominant In (Lu) blood phenotype

Catalytic activity:Acyl-CoA + NADP(+) = trans-2

Defects in PEX5 are a cause of neonatal adrenoleukodystrophy (NALD)

suggesting a role in tumor development and metastasis

This gene encodes a DEAD box protein| which is an antigen recognized by autoimmune antibodies from a patient with watermelon stomach disease

AR (Acetyl Lys632) Rabbit Polyclonal Antibody, 50ul Recombinant Ab Production Heterozygous loss-of-function mutations in KLF1disease: Defects in AR are the cause of androgen insensitivity syndrome (AIS)

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