CIRH1A anticorps (AA 497-686)

N° du produit ABIN6138631

Détail du produit anti-CIRH1A anticorps

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

Épitope: AA 497-686

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CIRH1A est non-conjugé

Application: Western Blotting (WB)

Séquence: NWLAASGTSA GVHVYNVKQL KLHCTVPAYN FPVTAMAIAP NTNNLVIAHS DQQVFEYSIP DKQYTDWSRT VQKQGFHHLW LQRDTPITHI SFHPKRPMHI LLHDAYMFCI IDKSLPLPND KTLLYNPFPP TNESDVIRRR TAHAFKISKI YKPLLFMDLL DERTLVAVER PLDDIIAQLP PPIKKKKFGT

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 497-686 of human CIRH1A (NP_116219.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur CIRH1A

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

Autre désignation: CIRH1A (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: 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.,UTP4,CIRH1A,CIRHIN,NAIC,TEX292,Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,CIRH1A

Poids moléculaire: 64 kDa/69 kDa/76 kDa

ID gène: 84916

UniProt: Q969X6