mSIRK
Based on 2 publication(s) in Google Scholar
mSIRK (G-Protein βγ Binding Peptide) is an cell-permeable activator of ERK1/2, with EC50 of 2.5-5 μM. mSIRK disrupts the interaction between α and βγ subunits and promotes α subunit dissociation without stimulating nucleotide exchange.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.54%
- CAS 番号: 593267-11-9
- 分子式: C93H150N20O25
- 分子量:1948.31
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保管条件:
Sealed storage, away from moisture.
Powder -80°C, 2 years , -20°C, 1 year* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
MedChemExpress(MCE)の使用を引用している文献 mSIRK
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WB
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Cell Proliferation/Viability Assay
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Cell Migration/Invasion Assay
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WB
生物活性
mSIRK (1.2-30 μM, 1-30 min) can rapidly activate extracellular signal-regulated kinases 1/2, stimulates the phosphorylation of Jun N-terminal kinase, the phosphorylation of p38 mitogen-activated protein kinase and the activity of phospholipase C, and leads to the internal storage and release of Ca2+[1].
mSIRK (10 μM, 24 h) rescues the inhibitory effect on cell proliferation and migration induced by Y27632 (HY-10071)[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:RASM, ddtMF2, MDA, Rat2, HEK293, COS7
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Concentration:1.2, 2.5, 5, 10, 30 μM
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Incubation Time:1, 2, 5, 10, 15, 30 min
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Result:Led to rapid and dose-dependent activation of ERK1/2.
Reached full activation after 1 minute of application and weakens within 30 minutes.
The phosphorylation of p38 MAP kinase and Jun kinase increased.
The activation degree of ERK1/2 depends on the cell type.
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Cell Line:SCC9 cell
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Concentration:10 μM
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Incubation Time:24 h
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Result:Partially rescued the inhibitory effect on cell proliferation and migration induced by Y27632.
化学情報
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CAS 番号 593267-11-9
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性状 Solid
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分子量 1948.31
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分子式 C93H150N20O25
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Color White to off-white
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配列
{Myr}-Ser-Ile-Arg-Lys-Ala-Leu-Asn-Ile-Leu-Gly-Tyr-Pro-Asp-Tyr-Asp
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シーケンスの短縮
{Myr}-SIRKALNILGYPDYD
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Sealed storage, away from moisture
Powder -80°C 2 years -20°C 1 year * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Publications (2)
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Journal Impact Factor
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Most Recent
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Int Immunopharmacol
Novel analgesic peptide derived from Cinobufacini injection suppressing inflammation and pain via ERK1/2/COX-2 pathway. [Abstract]2024 Nov 15:141:112918. PMID: 39159558
mSIRK purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2024 Nov 15:141:112918. [Abstract]
Western Blotting images of Rac-2, ERK 1/2, p-ERK 1/2 and COX-2 proteins in mSIRK (5 μM; 3 h then further co-cultured with CI5 for another 12 h) TFA-treated RAW264.7 macrophages treated with different concentration (100, 150 and 200 μg/mL) of CI5 for 12 h.
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mSIRK purchased from MedChemExpress. Usage Cited in: Oncologie. 2024 Oct 11;26(6).
CCK8 was performed to detect the cell viability of SCC9 cells treated with Y27632, ERK/JNK inhibitors (mSIRK (10 μM), ect.) or in combination for 72 h.
mSIRK purchased from MedChemExpress. Usage Cited in: Oncologie. 2024 Oct 11;26(6).
Wound healing assay of cells with treatment of Y27632, ERK/JNK inhibitors (mSIRK (10 μM), ect.) or in combination. Scale bar: 20 μm.
mSIRK purchased from MedChemExpress. Usage Cited in: Oncologie. 2024 Oct 11;26(6).
Western blot analysis of indicated protein level in mutp53 SCC9 cells treated with Y27632, mSIRK (24 h) (ERK activator, 10 μM) or Anisomycin (JNK activator, 10 μM).
溶剤 & 溶解度
DMSO : 100 mg/mL (51.33 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
純度とドキュメンテーション
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データシート (276 KB)
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SDS (252 KB)
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- Français - FR (252 KB)
- Deutsch - DE (252 KB)
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- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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取扱説明書 (2659 KB)
参考文献
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 0.5133 mL | 2.5663 mL | 5.1327 mL | 12.8316 mL |
| 5 mM | 0.1027 mL | 0.5133 mL | 1.0265 mL | 2.5663 mL | |
| 10 mM | 0.0513 mL | 0.2566 mL | 0.5133 mL | 1.2832 mL | |
| 15 mM | 0.0342 mL | 0.1711 mL | 0.3422 mL | 0.8554 mL | |
| 20 mM | 0.0257 mL | 0.1283 mL | 0.2566 mL | 0.6416 mL | |
| 25 mM | 0.0205 mL | 0.1027 mL | 0.2053 mL | 0.5133 mL | |
| 30 mM | 0.0171 mL | 0.0855 mL | 0.1711 mL | 0.4277 mL | |
| 40 mM | 0.0128 mL | 0.0642 mL | 0.1283 mL | 0.3208 mL | |
| 50 mM | 0.0103 mL | 0.0513 mL | 0.1027 mL | 0.2566 mL |