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- rabbit polyclonal IgG, 200 µg/ml
- epitope corresponding to amino acids 321-395 mapping within an internal region of NFATc3 of mouse origin
- recommended for detection of NFATc3 of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA; also reactive with additional species, including equine, canine and bovine
- TransCruz reagent for Gel Supershift and ChIP applications, sc-8321 X, 200 µg/0.1 ml
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NFATc3 Background Information Members of the NFAT (nuclear factor of activated T cells) family of transcription factors are related to NFkB/Rel proteins and form cooperative complexes with the AP-1 proteins, Fos and Jun, on DNA to regulate cytokine expression in T cells. NFAT proteins are widely expressed and alternatively modified to generate splice variants, and they are localized to both the cytosol (NFATc) and to the nucleus (NFATn). NFAT1, NFAT2 and NFAT4 are predominantly expressed in immune cells, and NFAT2 and NFAT3 are expressed at high levels in cardiac tissues. In addition to activating cytokine gene transcription, NFAT2 is also implicated in cardiac valve development and NFAT3 is involved in cardiac hypertrophy. NFAT5 is detected in both immune and nonimmune cells and, like other NFAT proteins, it contains a highly conserved Rel-like binding domain that mediates NFAT proteins associating with specific consensus sequences on DNA. NFAT proteins are activated by increases in intracellular calcium, which leads to the calmodulin-dependent phosphatase, calcineurin, dephosphorylating NFAT proteins. This activating event induces a conformational change in the protein structure that exposes the nuclear localization signal and facilitates the translocation of NFAT proteins from the cytosol into the nucleus.
| NFATc3 (M-75) Product Citations |
See how others have used NFATc3 (M-75): sc-8321 antibody and or NFATc3 (M-75) antibody conjugates.
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NFATc3 (M-75)
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NFATc3 (M-75): sc-8321. Western blot analysis of NFATc3 isoform expression in Ramos whole cell lysate.
Western blot analysis of NFATc3 phosphorylation in untreated (A,C) and IL-2-treated (B,D) Jurkat whole cell lysates. Antibodies tested include p-NFATc3 (Ser 265): sc-32982- (A,B) and NFATc3 (M-75): sc-8321 (C,D).
Western blot analysis of NFATc3 phosphorylation in untreated (A,B,D,E) and lambda protein phosphatase ( sc-200312A) treated (C,F) Jurkat whole cell lysates (A,C,D,F) and Jurkat nuclear extracts (B,E). Antibodies tested include p-NFATc3 (A-1): sc-365785 (A,B,C) and NFATc3 (M-75): sc-8321 (D,E,F).
Western blot analysis of NFATc3 phosphorylation in untreated (A,B,D,E) and lambda protein phosphatase ( sc-200312A) treated (C,F) Jurkat whole cell lysates (A,C,D,F) and Jurkat nuclear extracts (B,E). Antibodies tested include p-NFATc3 (Ser 344): sc-32983 (A,B,C) and NFATc3 (M-75): sc-8321 (D,E,F).
Western blot analysis of NFATc3 phosphorylation in untreated (A,C) and lambda protein phosphatase ( sc-200312A) treated (B,D) Jurkat whole cell lysates. Antibodies tested include p-NFATc3 (H-2): sc-365883 (A,B) and NFATc3 (M-75): sc-8321 (C,D).
Western blot analysis of NFATc3 phosphorylation in untreated (A,C) and lambda protein phosphatase ( sc-200312A) treated (B,D) Jurkat whole cell lysates. Antibodies tested include p-NFATc3 (Ser 169): sc-68701 (A,B) and NFATc3 (M-75): sc-8321 (C,D).
NFATc3 (M-75): sc-8321. Immunoperoxidase staining of formalin fixed, paraffin-embedded human stomach tissue showing cytoplasmic staining of glandular cells
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