Translational Control
| CSTコード |
包装 |
希望納入価格(円) |
国内在庫  |
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| #2317 | 100μL | 46,000 | |
|
推奨プロトコール
最適な結果を得るために:Cell Signaling Technology (CST) 社は、各製品の推奨プロトコールを使用することを強くお薦めいたします。
推奨プロトコールはCST社内試験の徹底的なバリデーションに基づいて作成されておりますので、正確かつ再現性の高い結果が得られます。
注:各製品に最適化されたプロトコールをリンクしています。
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2317:
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Flow
IHC / Paraffin
Immunofluorescence
Immunoprecipitation
Western Blotting
| 用途(希釈倍率) | |
| ウエスタンブロッティング(1:1,000)、免疫沈降(1:100)、免疫組織染色(パラフィン)(1:100)、免疫蛍光細胞染色(IF-IC)(1:25)、フローサイトメトリー(1:25) |
| 種交差性 | |
| ヒト、マウス、ラット、サル、、キイロショウジョウバエ |
| 特異性・感度 | |
| リン酸化に係わらず内在性レベルのS6 Ribosomal Protein を検出します。 |
| 使用抗原 | |
| GST と S6 Ribosomal Protein (full length)の融合タンパク質 |
| ※括弧付きの動物種は配列が100%相同であるため反応すると推定されます。 |
Western Blotting
Western blot analysis of extracts from HeLa, NIH/3T3, PC12 and COS cells, using S6 Ribosomal Protein (54D2) Mouse mAb.
IHC-P (paraffin)
Immunohistochemical analysis of paraffin-embedded human breast carcinoma, showing cytoplasmic localization, using S6 Ribosomal Protein (54D2) Mouse mAb.
IHC-P (paraffin)
Immunohistochemical analysis of paraffin-embedded human colon carcinoma, using S6 Ribosomal Protein (54D2) Mouse mAb.
IHC-P (paraffin)
Immunohistochemical analysis of paraffin-embedded LNCaP cells, using S6 Ribosomal Protein (54D2) Mouse mAb.
IHC-P (paraffin)
Immunohistochemical analysis of paraffin-embedded human lung carcinoma, using S6 Ribosomal Protein (54D2) Mouse mAb.
Flow Cytometry
Flow cytometric analysis of NIH/3T3 cells, using S6 Ribosomal Protein (54D2) Mouse mAb (blue) compared to a nonspecifc negative control antibody (red).
IF-IC
Confocal immunofluorescent images of HeLa cells labeled with S6 Ribosomal Protein (54D2) Mouse mAb (red, left) compared to an isotype control (right). Actin filaments have been labeled with fluorescein phalloidin. Blue pseudocolor = DRAQ5™ (fluorescent DNA dye).
One way that growth factors and mitogens effectively promote sustained cell growth and proliferation is by upregulating mRNA translation (1,2). Growth factors and mitogens induce the activation of p70 S6 kinase and the subsequent phosphorylation of the S6 ribosomal protein. Phosphorylation of S6 ribosomal protein correlates with an increase in translation of mRNA transcripts that contain an oligopyrimidine tract in their 5' untranslated regions (2). These particular mRNA transcripts (5'TOP) encode proteins involved in cell cycle progression as well as ribosomal proteins and elongation factors necessary for translation (2,3). Important S6 ribosomal protein phosphorylation sites include several residues (Ser235, Ser236, Ser240 and Ser244) located within a small, carboxy-terminal region of the S6 protein (4,5).
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Dufner, A. and Thomas, G. (1999)
Exp. Cell Res.
253, 100-109.
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Peterson, R.T. and Schreiber, S.L. (1998)
Curr. Biol.
8, R248-R250.
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Jefferies, H.B. et al. (1997)
EMBO J.
16, 3693-3704.
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Ferrari, S. et al. (1991)
J. Biol. Chem.
266, 22770-22775.
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Flotow, H. and Thomas, G. (1992)
J. Biol. Chem.
267, 3074-3078.