RFT1 rabbit pAb
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],
Product Specifications
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]
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
Available Sizes
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