CIRH1A polyclonal, anti-human, mouse

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.

Synonyms: UTP4, CIRH1A, CIRHIN, NAIC, TEX292,

Cellular Location: Nucleus nucleolus

Immunogen:
Recombinant protein of human CIRH1A

Gene Symbol: CIRH1A

Gene ID: 84916

Swiss prot: Q969X6

Calculated MW: 77kDa

Recommended dilution:
WB 1:500-2000

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.