CIRH1A anticorps (N-Term)

N° du produit ABIN951532

Détail du produit anti-CIRH1A anticorps

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

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CIRH1A est non-conjugé

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

Specificité: This antibody reacts to CIRH1A.

Réactivité croisée (Details): Species reactivity (tested):Human.

Purification: Affinity chromatography on Protein A

Immunogène: KLH conjugated synthetic peptide selected from the N-terminal region of human CIRH1A

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS, 0.09 % (W/V) sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur CIRH1A

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

Autre désignation: Cirhin (CIRH1A Produits)

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

Sujet: 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.Synonyms: CIRH1A, KIAA1988

Poids moléculaire: 76890 Da

ID gène: 84916

NCBI Accession: NP_116219