PEX13 rabbit pAb

• Background :

  Peroxisomal biogenesis factor 13 (PEX13) Homo sapiens This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]

• Description :

  Peroxisomal biogenesis factor 13 (PEX13) Homo sapiens This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008],

• UniProt :

  Q92968

• Swiss Prot :

  Q92968

• Reactivity :

  Human; Mouse

• Immunogen :

  Synthesized peptide derived from human protein . at AA range: 290-370

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000 ELISA 1:5000-20000

• Molecular Weight :

  44kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  44kD

• Fragment :

  IgG

• Subcellular Location :

  Peroxisome membrane ; Single-pass membrane protein .

• Gene ID (Human) :

  5194