FosB Antibody

FosB Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年09月05日
  • W, IP, IF-IC
  • Rabbit
  • H,M,R
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    • 详细信息
    • 技术资料
    • 抗体英文名

      FosB Antibody

    • 抗原

      synthetic peptide corresponding to the sequence of human FosB

    • 应用范围

      W, IP, IF-IC

    • 宿主

      Rabbit

    • 适应物种

      H,M,R

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 供应商

      CST

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation  IF-IC=Immunofluorescence (Immunocytochemistry)
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W IP IF-IC H M R Endogenous 38 FosB2. 48 FosB. Rabbit
    Protocols
    Specificity / Sensitivity

    This antibody detects endogenous levels of total FosB protein (both FosB and FosB2 isoforms). The antibody does not cross-react with other Fos proteins, including c-fos, FRA1 and FRA2.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human FosB. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells serum-starved overnight and TPA-stimulated for 4 hours or NIH/3T3 cells serum-starved overnight and serum-stimulated for 4 hours, using FosB Antibody.

    IF-IC

    IF-IC

    Immunofluorescent analysis of paraformaldehyde-fixed HeLa cells starved overnight (left panels) and stimulated for 4 hours with TPA (right panels). Cells were stained with DAPI (upper panels) and analyzed by IF using FosB Antibody (lower panels).

    Background

    The Fos family of nuclear oncogenes includes c-Fos, FosB, Fos-related antigen 1 (FRA1), and Fos-related antigen 2 (FRA2) (1). While most Fos proteins exist as a single isoform, the FosB protein exists as two isoforms: full-length FosB and a shorter form, FosB2 (Delta FosB), that lacks the carboxy-terminal 101 amino acids (1-3). The expression of Fos proteins is rapidly and transiently induced by a variety of extracellular stimuli including growth factors, cytokines, neurotransmitters, polypeptide hormones, and stress. Fos proteins dimerize with Jun proteins (c-Jun, JunB, and JunD) to form Activator Protein-1 (AP-1), a transcription factor that binds to TRE/AP-1 elements and activates transcription. Fos and Jun proteins contain the leucine-zipper motif that mediates dimerization and an adjacent basic domain that binds to DNA. The various Fos/Jun heterodimers differ in their ability to transactivate AP-1 dependent genes. In addition to increased expression, phosphorylation of Fos proteins by Erk kinases in response to extracellular stimuli may further increase transcriptional activity (4-6). Phosphorylation of c-Fos at Ser32 and Thr232 by Erk5 increases protein stability and nuclear localization (5). Phosphorylation of FRA1 at Ser252 and Ser265 by Erk1/2 increases protein stability and leads to overexpression of FRA1 in cancer cells (6). Following growth factor stimulation, expression of FosB and c-Fos in quiescent fibroblasts is immediate, but very short-lived, with protein levels dissipating after several hours (7). FRA1 and FRA2 expression persists longer, and appreciable levels can be detected in asynchronously growing cells (8). Deregulated expression of c-Fos, FosB, or FRA2 can result in neoplastic cellular transformation; however, Delta FosB lacks the ability to transform cells (2,3).

    1. Tulchinsky, E. (2000) Histol. Histopathol. 15, 921-928.
    2. Dobrzanski, P. et al. (1991) Mol. Cell. Biol. 11, 5470-5478.
    3. Nakabeppu, Y. and Nathans, D. (1991) Cell 64, 751-759.
    4. Rosenberger, S.F. et al. (1999) J. Biol. Chem. 274, 1124-1130.
    5. Sasaki, T. et al. (2006) Mol. Cell 24, 63-75.
    6. Basbous, J. et al. (2007) Mol. Cell. Biol. 27, 3936-3950.
    7. Kovary, K. and Bravo, R. (1991) Mol. Cell. Biol. 11, 2451-2459.
    8. Kovary, K. and Bravo, R. (1992) Mol. Cell. Biol. 12, 5015-5023.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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