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cirrhosis, autosomal recessive 1A (cirhin), Mouse, Polyclonal Antibody, Abnova™
Shop All Abnova Corporation ProductsDescription
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. [provided by RefSeq
Specifications
Specifications
| Antigen | cirrhosis, autosomal recessive 1A (cirhin) |
| Applications | ELISA, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a partial recombinant CIRH1A. |
| Formulation | 50% glycerol |
| Gene | CIRH1A |
| Gene Accession No. | NM_032830 |
| Gene Alias | CIRHIN/FLJ14728/FLJ17146/KIAA1988/NAIC/TEX292 |
| Gene Symbols | CIRH1A |
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