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CIRH1A antibody (N-Term)
The Rabbit Polyclonal anti-CIRH1A antibody has been validated for WB, FACS and IHC (p). It is suitable to detect CIRH1A in samples from Human.
Quick Overview for CIRH1A antibody (N-Term) (ABIN653909)
Target
See all CIRH1A Antibodies
CIRH1A
(Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
Reactivity
All reactivities for CIRH1A antibodies
Human
Host
All hosts for CIRH1A antibodies
Rabbit
Clonality
All clonalities for CIRH1A antibodies
Polyclonal
Conjugate
All conjugates for CIRH1A antibodies
This CIRH1A antibody is un-conjugated
Application
All applications for CIRH1A antibodies
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Clone
RB23136
Product Details anti-CIRH1A Antibody
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Binding Specificity
All epitopes for CIRH1A antibodies
AA 116-143, N-Term
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.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50
Restrictions
For Research Use only
Handling
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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
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Target
CIRH1A
(Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
Alternative Name
CIRH1A
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
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