MAP Kinase Signaling
p44/42 MAPK (Erk1/2) (L34F12) Mouse mAb
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| CSTコード |
包装 |
希望納入価格 (円) |
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| #4696S | 100 μL | 46,000 | |
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MAPK抗体製品一覧
4696 の推奨プロトコール
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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4696:
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Flow
IHC / Paraffin
Immunofluorescence
Western Blotting
下記ステップについては、データシートの右側もあわせてご参照ください。
IHC-P: 抗体希釈液 / 抗原賦活化
| 用途(希釈倍率) | |
| ウェスタンブロッティング(1:2,000)、免疫組織染色(パラフィン)(1:500)、免疫蛍光細胞染色(IF-IC)(1:50)、フローサイトメトリー(1:200) |
| 種交差性 | |
| ヒト、マウス、ラット、サル、ミンク、ブタ、ゼブラフィッシュ |
| 特異性・感度 | |
| 内在性レベルのp44/42 MAP Kinase を検出します。いくつかの手法ではp44/42 MAP Kinase より簡単にp42/Erk2 を認識します。JNK/SAPK および p38 MAP Kinase とは交差しません。 |
| 検出タンパク質の分子量 | |
| 42 kDa、44 kDa |
| 使用抗原 | |
| ラットのp44/42 MAP Kinase の配列(合成ペプチド) |
Western Blotting

Western blot analysis of extracts from NIH/3T3, PC12 and COS cells, using p44/42 MAP Kinase (L34F12) Mouse mAb.
IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using p44/42 MAP Kinase (L34F12) Mouse mAb in the presence of control peptide (left) or p44/42 MAP Kinase Blocking Peptide (#4696 Specific) #1245 (right).
IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human colon carcinoma, showing cytoplasmic and nuclear localization, using p44/42 MAP Kinase (L34F12) Mouse mAb.
Flow Cytometry

Flow cytometric analysis of Jurkat cells, U0126-treated (blue) or PMA-treated (green), using p44/42 MAP Kinase (L34F12) Mouse mAb compared to a nonspecific negative control antibody (red).
IF-IC

Confocal immunofluorescent analysis of NIH/3T3 cells, either U0126-treated (#9903, 10 μM, 2 hour, left) or PDGF-treated (#9909, 100 ng/ml, 20 min, right), using p44/42 MAP Kinase (L34F12) Mouse mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red).
Mitogen-activated protein kinases (MAPKs) are a widely conserved family of serine/threonine protein kinases involved in many cellular programs such as cell proliferation, differentiation, motility, and death. The p44/42 MAPK (Erk1/2) signaling pathway can be activated in response to a diverse range of extracellular stimuli including mitogens, growth factors, and cytokines (1-3) and is an important target in the diagnosis and treatment of cancer (4). Upon stimulation, a sequential three-part protein kinase cascade is initiated, consisting of a MAP kinase kinase kinase (MAPKKK or MAP3K), a MAP kinase kinase (MAPKK or MAP2K), and a MAP kinase (MAPK). Multiple p44/42 MAP3Ks have been identified, including members of the Raf family as well as Mos and Tpl2/Cot. MEK1 and MEK2 are the primary MAPKKs in this pathway (5,6). MEK1 and MEK2 activate p44 and p42 through phosphorylation of activation loop residues Thr202/Tyr204 and Thr185/Tyr187, respectively. Several downstream targets of p44/42 have been identified, including p90RSK (7) and the transcription factor Elk-1 (8,9). p44/42 are negatively regulated by a family of dual-specificity (Thr/Tyr) MAPK phosphatases, known as DUSPs or MKPs (10), along with MEK inhibitors such as U0126 and PD98059.
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Roux, P.P. and Blenis, J. (2004) Microbiol Mol Biol Rev 68, 320-44.
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Baccarini, M. (2005) FEBS Lett 579, 3271-7.
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Meloche, S. and Pouysségur, J. (2007) Oncogene 26, 3227-39.
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Roberts, P.J. and Der, C.J. (2007) Oncogene 26, 3291-310.
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Rubinfeld, H. and Seger, R. (2005) Mol Biotechnol 31, 151-74.
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Murphy, L.O. and Blenis, J. (2006) Trends Biochem Sci 31, 268-75.
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Dalby, K.N. et al. (1998) J Biol Chem 273, 1496-505.
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Marais, R. et al. (1993) Cell 73, 381-93.
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Kortenjann, M. et al. (1994) Mol Cell Biol 14, 4815-24.
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Owens, D.M. and Keyse, S.M. (2007) Oncogene 26, 3203-13.