CIRH1A Antibody (N-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP9951a
Background:
CIRH1A 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.
Other Names:
Cirhin, CIRH1A, KIAA1988, UTP4
Gene Name: UTP4 (HGNC:1983)
Gene ID: 84916
Primary Accession: Q969X6
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
CIRH1A 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.
Other Names:
Cirhin, CIRH1A, KIAA1988, UTP4
Gene Name: UTP4 (HGNC:1983)
Gene ID: 84916
Primary Accession: Q969X6
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
| Is Featured? | No |
|---|
Write Your Own Review