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PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are
PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are
PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are
PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are

PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are

SKU: 66340739947

4.9
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PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are

Store: jftbasic.com · Domain: jftbasic.com

Description

Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

This gene encodes an epsilon subunit

The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities

also referred to as Ullrich scleroatonic muscular dystrophy

The canonical alpha isoform of the encoded protein is a disulfide-linked homodimer whose activity is mediated by a G-protein-coupled phosphatidylinositol-calcium second messenger system

PRR22 Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Defects in this gene are

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