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Progesterone Receptor A/B (C89

F7) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月27日
  • W, IHC-P
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Progesterone Receptor A/B (C89F7) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues surrounding Tyr541 of human progesterone receptor

    • 应用范围

      W, IHC-P

    • 适应物种

      H

    • 供应商

      CST

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 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  IHC-P=Immunohistochemistry (Paraffin)
    Reactivity Key:  H=Human
    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 IHC-P H Endogenous 90 (PR-A) and 118 (PR-B) Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Progesterone Receptor A/B (C89F7) Rabbit mAb detects endogenous levels of total progesterone receptor A and B proteins. This antibody does not cross-react with other PR family members.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Tyr541 of human progesterone receptor.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from T47D cells using Progesterone Receptor A/B (C89F7) Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Progesterone Receptor A/B (C89F1) Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded T47D cells (positive, left) and MDA-MB-231 cells (negative, right) using Progesterone Receptor A/B (C89F1) Rabbit mAb.


    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Progesterone Receptor A/B (C89F1) Rabbit mAb in the presence of control peptide (left) or antigen-specific peptide (right).

    Background

    Human progesterone receptor (PR) is expressed as two forms: the full length PR B and the short form PR A. PR A lacks the first 164 amino acid residues of PR B (1,2). Both PR A and PR B are ligand activated but differ in their relative ability to activate target gene transcription (3,4). The activity of PR is regulated by phosphorylation; at least seven serine residues are phosphorylated in its amino-terminal domain. Three sites (Ser81, Ser102 and Ser162) are unique to full length PR B while other sites (Ser190, Ser294, Ser345 and Ser400) are shared by both isoforms (5). Phosphorylation of PR B at Ser190 (equivalent to Ser26 of PR A) is catalyzed by CDK2 (6). Mutation of Ser190 results in decreased activity of PR (7), suggesting that the phosphorylation of Ser190 may be critical to its biological function.

    1. Evans, R.M. (1988) Science 240, 889-895.
    2. Kastner, P. et al. (1990) EMBO J. 112, 1603-1614.
    3. Giangrande, P.H. et al. (2000) Mol. Cell. Biol. 20, 3102-3115.
    4. Wen, D.X. et al. (1994) Mol. Cell. Biol. 14, 8356-8364.
    5. Clemm, D.L. et al. (2000) Mol. Endocrinol. 14, 52-65.
    6. Zhang, Y. et al. (1997) Mol. Endocrinol. 11, 823-832.
    7. Takimoto, G.S. et al. (1996) J. Biol. Chem. 271, 13308-13316.
    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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