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Phospho-FRA1 (Ser265) (D22B1)

Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月25日
  • W
  • H,M,R,Mk,B,Hr
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-FRA1 (Ser265) (D22B1) Rabbit mAb

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Ser265 of human FRA1 protein

    • 应用范围

      W

    • 库存

      大量

    • 适应物种

      H,M,R,Mk,B,Hr

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 保质期

      详见说明书

    • 是否单克隆

      1

    • 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
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  B=Bovine  Hr=Horse
    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) Isotype
    W H M R (Mk) (B) (Hr) Endogenous 40 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Phospho-FRA1 (Ser265) (D22B1) Rabbit mAb recognizes endogenous levels of FRA1 protein only when phosphorylated at Ser265. This antibody may also cross-react with phospho-FRA2, but does not cross-react with phospho-c-Fos or phospho-FosB.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser265 of human FRA1 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells, serum-starved overnight, and either left untreated or treated with TPA #4174 for 4 hours, using Phospho-FRA1 (Ser265) (D22B1) Rabbit mAb #5841 (upper) and FRA1 (D80B4) Rabbit mAb #5281 (lower). Antibody phospho-specificity is shown by treating lysates with λ phosphatase.

    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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    图标文献和实验
    相关实验
    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      :使用 Anti-phospho-Akt (Ser473) Rabbit mAb 对石蜡包埋的人乳腺癌组织进行免疫组织化学分析。(图 A)使用免疫组化试剂盒M&R HRP/DAB Detection IHC Kit,抗体 1:100 稀释;(图 B) 采用普通免疫组化试剂盒,抗体 1:25 稀释。 图 6 免疫组化实验检测 Erk1/2 表达 注:使用 Anti-Erk1/2 Mouse mAb与p44/42 MAPK (Erk1/2)Rabbit mAb 对正常小鼠心脏组织进行免疫

    • Using Phospho‐Motif Antibodies to Determine Kinase Substrates

      ., Graves, D.J., DeMaggio, A.J., Hoekstra, M.F., Blenis, J., Hunter, T., and Cantley, L.C. 1996. A structural basis for substrate specificities of protein Ser/Thr kinases: Primary sequence preference of. casein kinases I and II, NIMA, phosphorylase kinase

    • 【求助】磷酸化的Akt不见了!!

      (Ser473)(193H12)Rabbit mAb,1:300,稀释,二抗是驴抗兔,1:2000,我是实验室的新手,刚呆俩月,受 此挫折,一头雾水,请过来人或者有经验的同学帮忙解答怎样解决,非常感谢! 碧峤 pAkt有两个位点,Ser473和Thr308,其中Ser473相对容易显色。如果显色失败,可能的原因:1 上样量过少,我们一般都是30μg;2 一抗孵育时间过短,我们一般24h~48h;3 一抗是否工作有待排除 米宝

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