328000 Sigma-AldrichERK Activation Inhibitor Peptide I, Cell-Permeable - Calbiochem
The ERK Activation Inhibitor Peptide I, Cell-Permeable controls the biological activity of ERK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
More>> The ERK Activation Inhibitor Peptide I, Cell-Permeable controls the biological activity of ERK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Less<<同義語: Ste-MEK1₁₃, Ste-MPKKKPTPIQLNP-NH₂, Erk Inhibitor IV
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概要
| Replacement Information |
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主要スペック表
| Empirical Formula |
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| C₈₆H₁₅₃N₁₉O₁₇S |
価格&在庫状況
| カタログ番号 | 在庫状況 | 包装 | Qty/Pk | 価格 | 数量 | |
|---|---|---|---|---|---|---|
| 328000-1MGCN |
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樹脂アンプル | 1 mg |
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| References | |
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| References | Kelemen, B.R., et al. 2002. J. Biol. Chem. 277, 8741. |
| Product Information | |
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| ATP Competitive | N |
| Form | White lyophilized solid |
| Formulation | Supplied as a trifluoroacetate salt. |
| Hill Formula | C₈₆H₁₅₃N₁₉O₁₇S |
| Chemical formula | C₈₆H₁₅₃N₁₉O₁₇S |
| Hygroscopic | Hygroscopic |
| Reversible | Y |
| Quality Level | MQ100 |
| Applications |
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| Biological Information | |
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| Primary Target | MEK |
| Primary Target IC<sub>50</sub> | 2.5 µM |
| Purity | ≥95% by HPLC |
| Physicochemical Information | |
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| Cell permeable | Y |
| Peptide Sequence | Ste-Met-Pro-Lys-Lys-Lys-Pro-Thr-Pro-Ile-Gln-Leu-Asn-Pro-NH₂ (Ste = stearated) |
| Dimensions |
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| Materials Information |
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| Toxicological Information |
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| Safety Information according to GHS |
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| Safety Information |
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| Product Usage Statements |
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| Packaging Information | |
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| Packaged under inert gas | Packaged under inert gas |
| Transport Information |
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| Supplemental Information |
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| Specifications |
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| Global Trade Item Number | |
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| カタログ番号 | GTIN |
| 328000-1MGCN | 04055977196337 |
Documentation
ERK Activation Inhibitor Peptide I, Cell-Permeable - Calbiochem (M)SDS
| タイトル |
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ERK Activation Inhibitor Peptide I, Cell-Permeable - Calbiochem 試験成績書(CoA)
| タイトル | ロット番号 |
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| 328000 |
参考資料
| 参考資料の概要 |
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| Kelemen, B.R., et al. 2002. J. Biol. Chem. 277, 8741. |



