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