CIRH1A anticorps
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- Antigène Voir toutes CIRH1A Anticorps
- CIRH1A (Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CIRH1A est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human CIRH1A
- Isotype
- IgG
- Top Product
- Discover our top product CIRH1A Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- 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.
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- 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
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Synonyms: CIRH1A,Cirhin,Cirrhosis, autosomal recessive 1A (cirhin),FLJ17146,KIAA1988,NAIC,testis expressed gene 292,TEX292,U3 small nucleolar RNA associated protein 4 homolog,UTP4,UTP4 small subunit (SSU) processome component,UTP4 small subunit (SSU) processome component homolog,UTP4, small subunit processome component
Background: 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.
- Poids moléculaire
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Observed_MW: 77kDa
Calculated_MW: 64kDa/69kDa/76kDa
- ID gène
- 84916
- UniProt
- Q969X6
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