RFT1 rabbit pAb

• Background :

  This gene encodes an enzyme which catalyzes the translocation of the Man (5) GlcNAc (2) -PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]

• Description :

  This gene encodes an enzyme which catalyzes the translocation of the Man (5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In. [provided by RefSeq, Dec 2008],

• UniProt :

  Q96AA3

• Swiss Prot :

  Q96AA3

• Reactivity :

  Human; Mouse

• Immunogen :

  Synthesized peptide derived from human RFT1 AA range: 451-501

• Target :

  RFT1

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000

• Buffer :

  -20°C/1 year

• Storage Conditions :

  -20°C/1 year

• Fragment :

  IgG

• Subcellular Location :

  Membrane ; Multi-pass membrane protein .

• Gene ID (Human) :

  91869