CIR1A rabbit pAb
This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016],
Product Specifications
Background
This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
UniProt
Q969X6
Swiss Prot
Q969X6
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human CIR1A AA range: 313-363
Target
CIR1A
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
Nucleus, nucleolus . Chromosome . Found predominantly at the fibrillar center. .
Gene ID (Human)
84916
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
![Mouse Monoclonal KIR2DL1/KIR2DS5 Antibody (143211) [Janelia Fluor 525]](https://cdn.genprice.uk/genprice/uk/genprice2.webp)
FAB1844JF525 0.1 mL
Mouse Monoclonal KIR2DL1/KIR2DS5 Antibody (143211) [Janelia Fluor 525]
Sign In for Pricing
View Details 