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CIR1A rabbit pAb

CAT: 0855-ES17452-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES17452-01Size:50 µL
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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]
Description
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