Cell Signaling Technology

Product Pathways - Nuclear Receptor Signaling

Phospho-Progesterone Receptor (Ser190) Antibody #3171


No. Size Price
3171S 100 µl ( 10 western blots ) ¥4,050.00 现货查询 购买询价 防伪查询
3171 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human, Endogenous 90, 118 Rabbit
IP 1:50

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation,

Specificity / Sensitivity

Phospho-Progesterone Receptor (Ser190) Antibody detects endogenous levels of both progesterone receptor B and A forms only when phosphorylated at serine 190 and serine 26, respectively. This antibody does not cross-react with other PR family members.只有当丝氨酸(190和26位)磷酸化时,Phospho-Progesterone Receptor (Ser190) Antibody能够分别检测内源性水平的孕酮受体B和A亚型蛋白。该抗体不与其他孕酮受体家族成员发生交叉反应。

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser190 of human progesterone receptor. Antibodies are purified by protein A and peptide affinity chromatography.该多克隆抗体通过用合成磷酸肽免疫动物制备,该合成磷酸肽是人孕酮受体丝氨酸(190位)附近的残基。抗体由蛋白A和肽亲和层析纯化。

Western Blotting

Western Blotting

Western blot analysis of extracts from T47D cells, untreated or stimulated with 100 nM promegestone (R5020) for 1 hour, using Phospho-Progesterone Receptor (Ser190) Antibody (upper) and control Progesterone Receptor Antibody #3172 (lower).Western blot方法检测T47D细胞提取物,细胞不处理或用100 nM普美孕酮(R5020)刺激处理1小时,使用的抗体为Phospho-Progesterone Receptor (Ser190) Antibody (上图)和control Progesterone Receptor Antibody #3172 (下图).


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.人孕酮受体(PR)表现为两种形式:全长的孕酮受体B和短的孕酮受体A。PR A缺少PR B的第164个氨基酸残基(1,2)。PR A和PR B都是配体激活,但其激活靶基因转录的相对能力是不同的(3,4)。PR的活性受磷酸化调节。在其氨基末端区域,至少有七个丝氨酸残基被磷酸化。丝氨酸三个位点(81,102,162位)是全长PR特有的,而其他丝氨酸位点(190,294,345和400位)是两个亚型所共有的(5)。PR B丝氨酸(190位)(相当于PR A丝氨酸(26位))的磷酸化是由CDK2催化的(6)。丝氨酸(190位)的突变导致PR活性降低(7),这表明丝氨酸(190位)的磷酸化对其生物功能来说是至关重要的。

  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

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