Anti-ZC3H7A Antibody B-3 è un monoclonale di topo IgG1 κ ZC3H7A antibody, citato in 1 pubblicazioni, fornito in 200 µg/ml
generato contro gli amminoacidi 885-948 mappati vicino al C-terminus di ZC3H7A di origine human
ZC3H7A Antibody (B-3) é raccomandato per il rilevamento di ZC3H7A di origine mouse, rat e human in WB, IP, IF e ELISA
ZC3H7A Antibody (B-3) é disponibile coniugato con agarose per IP; HRP per WB, IHC(P) ed ELISA; sia con phycoerythrin o FITC per IF, IHC(P) e FCM
disponibile anche coniugato con Alexa Fluor® 488, Alexa Fluor® 546; Alexa Fluor® 594 o Alexa Fluor® 647 per IF, IHC (P) e FCM
disponibile anche coniugato con Alexa Fluor® 680 o Alexa Fluor® 790 per WB (NIR), IF e FCM
Contattaci per ricevere un FREE 10 µg sample di ZC3H7A (B-3): sc-398981.
m-IgG1 BP-HRP (mouse IgG1 binding protein-HRP) is the preferred secondary detection reagent for ZC3H7A Antibody (B-3) for WB applications. This reagent is now offered in a bundle with ZC3H7A Antibody (B-3) (see ordering information below).
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Ships via FedEx Ground to Contiguous US, Alaska, Canada, Monday through Friday. This method is used for less temperature sensitive items such as lab ware and animal
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Labware ships FedEx Ground free of charge to the contiguous US
ZC3H7A Antibody (B-3) is a high quality monoclonal ZC3H7A antibody (also designated ZC3H7A antibody) suitable for the detection of the ZC3H7A protein of mouse, rat and human origin. ZC3H7A Antibody (B-3) is available as both the non-conjugated anti-ZC3H7A antibody form, as well as multiple conjugated forms of anti-ZC3H7A antibody, including agarose, HRP, PE, FITC and multiple Alexa Fluor® conjugates. 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.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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