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NSJ Bioreagents

SKU:V9472-20UG

ZC3H7A Antibody, 20 ug

ZC3H7A Antibody, 20 ug

Regular price $259.00 USD
Regular price Sale price $259.00 USD
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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.

Specifications

Catalog No V9472-20UG
Family Primary antibody
Qty 20 ug
Formulation 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
Format Purified
Clone PCRP-ZC3H7A-1D6
Host Animal Mouse
Clonality Monoclonal (mouse origin)
Isotype Mouse IgG1
Species Reactivity Human
Application ELISA, FACS, IF
Application Details ELISA (order BSA-free format for coating),Flow cytometry: 1-2ug/million cells,Immunofluorescence: 1-2ug/ml
Application Note Optimal dilution of the ZC3H7A antibody should be determined by the researcher.
Localization Nucleus, cytoplasm
Immunogen Recombinant full-length human ZC3H7A protein was used as the immunogen for the ZC3H7A antibody.
Purity Protein A/G affinity
Storage Aliquot the ZC3H7A antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Limitation This ZC3H7A antibody is available for research use only.
Uniprot # Q8IWR0
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/zc3h7a-antibody-pcrp-zc3h7a-1d6-v9472
Title ZC3H7A Antibody
Description 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.
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