ZC3H7A Polyclonal Antibody

For reference only. Please follow the manual included in your kit for instructions.

Catalog Number
RD81267A
Western blot analysis of extracts of various cell lines using ZC3H7A Polyclonal Antibody at dilution of 1:3000.
Western blot analysis of extracts of various cell lines using ZC3H7A Polyclonal Antibody at dilution of 1:3000.
Immunofluorescence analysis of C6 cells using ZC3H7A Polyclonal Antibody at dilution of  1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of C6 cells using ZC3H7A Polyclonal Antibody at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of HeLa cells using ZC3H7A Polyclonal Antibody at dilution of  1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of HeLa cells using ZC3H7A Polyclonal Antibody at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of L929 cells using ZC3H7A Polyclonal Antibody at dilution of  1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of L929 cells using ZC3H7A Polyclonal Antibody at dilution of 1:100. Blue: DAPI for nuclear staining.
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Overview

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Product Name
ZC3H7A Polyclonal Antibody
Catalog Number
RD81267A
Purification Method
Affinity purification
Isotype
IgG
Host
Rabbit

Background

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The zinc finger CCCH domain-containing protein 7A (ZC3H7A), also known as ZC3H7, HSPC055 or ZC3HDC7, is a 971 amino acid protein that contains a C3H1-type zinc finger domain, three C3H1-type zinc fingers and three TPR repeats. Belonging to the ZC3H12 family, ZC3H7A localizes to the nucleus. Existing as two alternatively spliced isoforms, ZC3H7A is encoded by a gene located on human chromosome 16p13.13. Chromosome 16 makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene.

Immunogen Information

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Immunogen
Recombinant fusion protein of human ZC3H7A (NP_054872.2).
Gene ID
29066
Swissprot
Q8IWR0
Synonyms
ZC3H7AHSPC055ZC3H7ZC3HDC7
Calculated MW
19 kDa/110 kDa
Observed MW
120 kDa

Applications

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Reactivity
Human,Mouse,Rat
Tested Applications
WB,IF
Conjugation
Unconjugated
Dilution
WB 1:500-1:2000 IF 1:50-1:200
Concentration
1 mg/mL
Storage Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Storage Instructions
Store at -20°C. Avoid freeze / thaw cycles.

Research Areas

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