CIRH1A antibody (N-Term)

Catalog No. ABIN653909

Product Details anti-CIRH1A Antibody

Target: CIRH1A (Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))

Binding Specificity: AA 116-143, N-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CIRH1A antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This CIRH1A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 116-143 amino acids from the N-terminal region of human CIRH1A.

Clone: RB23136

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

Target Details for CIRH1A

Target: CIRH1A (Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))

Alternative Name: CIRH1A (CIRH1A Products)

Synonyms: cirhin antibody, Cirhin antibody, Naic antibody, Teg-292 antibody, Tex292 antibody, naic antibody, tex292 antibody, zgc:77199 antibody, wu:fi09g10 antibody, wu:fi37c02 antibody, CIRH1A antibody, CIRHIN antibody, NAIC antibody, TEX292 antibody, UTP4 antibody, UTP4, small subunit processome component antibody, UTP4 small subunit processome component antibody, UTP4 small subunit processome component L homeolog antibody, UTP4 antibody, Utp4 antibody, utp4 antibody, utp4.L antibody

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.

Molecular Weight: 76890

Gene ID: 84916

NCBI Accession: NP_116219

UniProt: Q969X6