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
Gene ID
84916
UniProt
Q969X6
Cellular Locus
Nucleus, nucleolus. Chromosome. Found predominantly at the fibrillar center..
Host
Rabbit
Species Reactivity
Human,Mouse
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human CIR1A AA range: 313-363
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.
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES17452-1.pdf
Subcellular Location
Nucleus, nucleolus . Chromosome . Found predominantly at the fibrillar center. .
Gene ID (Human)
84916
SwissProt (Human)
Q969X6
Available Sizes
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