RRBP1 rabbit pAb
This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012],
Product Specifications
Background
UniProt
Q9P2E9
Swiss Prot
Q9P2E9
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human protein . at AA range: 1120-1200
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Molecular Weight
155kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
155kD
Fragment
IgG
Subcellular Location
Endoplasmic reticulum membrane ; Single-pass type III membrane protein .
Gene ID (Human)
6238
Available Sizes
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