MAP Kinase Signaling
MEK1/2 (L38C12) Mouse mAb |
イイネ!(0) |
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| CSTコード | 包装 | 希望納入価格 (円) |
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|---|---|---|---|---|
| #4694S | 100 μL | 46,000 | ログインすると国内在庫状況がご確認いただけます。
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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(1:1,000)、免疫組織染色(パラフィン)(1:25)、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 |
| 特異性・感度 | |
|---|---|
| 内在性レベルのMEK1/2 タンパク質を検出します。 |
| 検出タンパク質の分子量 | |
|---|---|
| 45 kDa |
| 使用抗原 | |
|---|---|
| 全長MEK1/2 タンパク質 |
| 抗体の由来 | |
|---|---|
| マウス |
| 貯法 | |
|---|---|
| -20℃ |
| 社内データ |
|---|
Western Blotting

Western blot analysis of extracts from NIH/3T3, PC12 and COS cells, using MEK1/2 (L38C12) Mouse mAb.
IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, showing cytoplasmic localization using MEK1/2 (L38C12) Mouse mAb.
IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human colon carcinoma, using MEK1/2 (L38C12) Mouse mAb.
IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human prostate carcinoma, using MEK1/2 (L38C12) Mouse mAb.
Flow Cytometry

Flow cytometric analysis of Jurkat cells, U0126-treated (blue) or PMA-treated (green), using MEK1/2 (L38C12) Mouse mAb compared to a nonspecific negative control antibody (red).
IF-IC

Confocal immunofluorescence images of untreated HeLa cells labeled with MEK1/2 (L38C12) Mouse mAb (red, left) compared to an isotype control (right). Actin filaments have been labeled with fluorescein phalloidin. Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).
| バックグラウンド |
|---|
MEK1 and MEK2, also called MAPK or Erk kinases, are dual-specificity protein kinases that function in a mitogen activated protein kinase cascade controlling cell growth and differentiation (1-3). Activation of MEK1 and MEK2 occurs through phosphorylation of two serine residues at positions 217 and 221, located in the activation loop of subdomain VIII, by Raf-like molecules. MEK1/2 is activated by a wide variety of growth factors and cytokines and also by membrane depolarization and calcium influx (1-4). Constitutively active forms of MEK1/2 are sufficient for the transformation of NIH/3T3 cells or the differentiation of PC-12 cells (4). MEK activates p44 and p42 MAP kinase by phosphorylating both threonine and tyrosine residues at sites located within the activation loop of kinase subdomain VIII.
| 使用例 | |
|---|---|
| 製品をご使用いただいて研究を発表されましたら、ぜひお知らせください。 |
本製品は試験研究用です。
