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],

• Gene ID:

  91869

• UniProt:

  Q96AA3

• Cellular Locus:

  Membrane ; Multi-pass membrane protein.

• Host:

  Rabbit

• Species Reactivity:

  Human, Mouse

• Reactivity:

  Human; Mouse

• Immunogen:

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

• Clonality:

  Polyclonal

• Isotype:

  IgG

• Source:

  Rabbit

• Applications:

  WB

• Validated Applications:

  WB

• Stability:

  -20°C/1 year

• Concentration:

  1 mg/mL

• Dilution:

  WB 1: 500-2000

• Storage Conditions:

  PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.

• Subcellular Location:

  Membrane ; Multi-pass membrane protein .

• Gene ID (Human):

  91869

• SwissProt (Human):

  Q96AA3