Target：GAS3

Gene Name：PMP22

Protein Name：Peripheral myelin protein 22

Human Gene Id：5376

Human Swiss Prot No：Q01453

Mouse Gene Id：18858

Mouse Swiss Prot No：P16646

Rat Gene Id：24660

Rat Swiss Prot No：P25094

Immunogen：The antiserum was produced against synthesized peptide derived from human PMP22. AA range:111-160

Specificity：GAS3 Polyclonal Antibody detects endogenous levels of GAS3 protein.

Formulation：Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source：Polyclonal, Rabbit,IgG

Dilution：WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Purification：The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration：1 mg/ml

Storage Stability：-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name：PMP22;GAS3;Peripheral myelin protein 22;PMP-22;Growth arrest-specific protein 3;GAS-3

Observed Band(KD)：22kD

Background： This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],

Function：disease:Defects in PMP22 are a cause of Dejerine-Sottas syndrome (DSS) [MIM:145900]; also known as Dejerine-Sottas neuropathy (DSN) or hereditary motor and sensory neuropathy III (HMSN3). DSS is a severe degenerating neuropathy of the demyelinating Charcot-Marie-Tooth disease category, with onset by age 2 years. DSS is characterized by motor and sensory neuropathy with very slow nerve conduction velocities, increased cerebrospinal fluid protein concentrations, hypertrophic nerve changes, delayed age of walking as well as areflexia. There are both autosomal dominant and autosomal recessive forms of Dejerine-Sottas syndrome.,disease:Defects in PMP22 are a cause of hereditary neuropathy with liability to pressure palsies (HNPP) [MIM:162500]; an autosomal dominant disorder characterized by transient episodes of decreased perception or peripheral nerve palsies after slight traction, compressi

Subcellular Location：Cell membrane ; Multi-pass membrane protein .

Expression： Fetal fibroblast,Kidney,Peripheral blood,Peripheral blood leukocyte,Spinal