gp91 ds-tat
Based on 1 publication(s) in Google Scholar
gp91 ds-tat, a biological active peptide, is a NADPH oxidase 2 (Nox2) inhibitor. gp91 ds-tat blocks NADPH oxidase-dependent superoxide production. gp91 ds-tat ameliorates high glucose-induced increase in total ROS, LPOs and iron levels. gp91 ds-tat inhibits homocysteine (Hcy)-induced activation of NLRP3 inflammasomes and restores Hcy-inhibited lysosomal TRPML1 channel activity. gp91 ds-tat improves cerebrovascular and cognitive function in APP/PS1 mice. gp91 ds-tat can be used for the study of Alzheimer’s disease (AD), glomerular inflammation and cardiovascular disease.
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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: 99.00%
- CAS 番号: 329902-61-6
- 分子式: C98H190N50O22S
- 分子量:2452.94
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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)
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生物活性
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化学情報
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溶剤 & 溶解度
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
MedChemExpress（MCE）の使用を引用している文献 gp91 ds-tat
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生物活性
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GPX4 |
gp91 ds-tat (5μM, 96 h) ameliorates high glucose-induced increase in total ROS, LPOs and iron levels, prevents inhibition of GPx4 activity, and attenuates cell death in human retinal endothelial cells[1].
gp91 ds-tat (5μM, 96 h) prevents impairments in mitochondrial membrane potential, decrease in oxygen consumption rate (including basal and maximal respiration rates), and reduction in mtDNA transcription and copy numbers in human retinal endothelial cells[1].
gp91 ds-tat (5 μM, 1 h pretreatment before homocysteine (Hcy) treatment) blocks Hcy-induced superoxide production in mouse podocytes[3].
gp91 ds-tat (5 μM, 1 h pretreatment before Hcy treatment) inhibits Hcy-induced activation of NLRP3 inflammasomes and formation of MVBs containing inflammatory cytokines in mouse podocytes[3].
gp91 ds-tat peptide (5 μM, 1 h pretreatment before Hcy treatment) restores Hcy-inhibited TRPML1 channel activity in mouse podocytes, reduces Hcy-enhanced exosome release from mouse podocytes and reverses the impaired lysosome-MVB interaction induced by Homocysteine in mouse podocytes[3].
gp91 ds-tat (1-3 μM, 2 h pretreatment) significantly inhibits chemerin-induced reactive oxygen species (ROS) production and inhibits chemerin-induced proliferation and migration in rat mesenteric arterial smooth muscle cells (SMCs)[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:mouse podocytes
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Concentration:5 μM
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Incubation Time:1 h pretreatment before Hcy treatment
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Result:Increased colocalization of NLRP3 with ASC and caspase-1 via confocal microscopy.
Enhanced colocalization of Rab7a/VPS16 with IL-1β.
Recovered ML-SA1-induced GCaMP3 fluorescence elevation.
Increased colocalization of Rab7a (MVB marker) and Lamp-1 (lysosome marker).
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:APP/PS1 transgenic mice (10-11 months old, both sexes) were used as a mouse model of Alzheimer's disease[2]
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Dosage:10 mg/kg
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Administration:i.p. every other day for 1 or 2 weeks
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Result:Reduced ROS accumulation and NOX2 mRNA expression in the neocortex of APP/PS1 mice.
Decreased capillary stalling incidence by 67% in APP/PS1 mice after 1 week.
Increased volumetric blood flow and RBC flow speed in penetrating arterioles of APP/PS1 mice.
Improved performance in object displacement and Y-maze tests (short-term and spatial memory) in APP/PS1 mice, with significant effects after 2 weeks.
Reduced GFAP expression in the hippocampus and IBA1 expression in cortex/hippocampus of APP/PS1 mice (neuroinflammation attenuation), without affecting amyloid-β levels.
Downregulated inflammatory and leukocyte adhesion-related pathways in cerebral microvessels of APP/PS1 mice.
Decreased VCAM-1 and ICAM-1 expression in penetrating arterioles and capillaries of APP/PS1 mice.
化学情報
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CAS 番号 329902-61-6
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性状 Solid
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分子量 2452.94
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分子式 C98H190N50O22S
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Color White to off-white
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配列
Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Cys-Ser-Thr-Arg-Ile-Arg-Arg-Gln-Leu-NH2
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シーケンスの短縮
RKKRRQRRRCSTRIRRQL-NH2
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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 (1)
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Journal Impact Factor
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Most Recent
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Rheumatology (Oxford)
Autophagy inhibitors block pathogenic NET release in immune-mediated inflammatory disease without impairing host defence. [Abstract]2025 Aug 13:keaf437. PMID: 40802538
溶剤 & 溶解度
DMSO : 100 mg/mL (40.77 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : ≥ 50 mg/mL (20.38 mM)
* "≥" means soluble, but saturation unknown.
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.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
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.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
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 (283 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Portuguese - PT (252 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Malaviya P, et al. Role of ferroptosis in mitochondrial damage in diabetic retinopathy. Free Radic Biol Med. 2024 Nov 20;225:821-832. [Content Brief]
[2]. Ruiz-Uribe NE, et al. Vascular oxidative stress causes neutrophil arrest in brain capillaries, leading to decreased cerebral blood flow and contributing to memory impairment in a mouse model of Alzheimer’s disease. bioRxiv [Preprint]. 2023 Feb 15:2023.02.15.528710. [Content Brief]
[3]. Li G, et al. Regulation of TRPML1 channel activity and inflammatory exosome release by endogenously produced reactive oxygen species in mouse podocytes. Redox Biol. 2021 Jul;43:102013. [Content Brief]
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 |
|---|---|---|---|---|---|
| H2O / DMSO | 1 mM | 0.4077 mL | 2.0384 mL | 4.0767 mL | 10.1919 mL |
| 5 mM | 0.0815 mL | 0.4077 mL | 0.8153 mL | 2.0384 mL | |
| 10 mM | 0.0408 mL | 0.2038 mL | 0.4077 mL | 1.0192 mL | |
| 15 mM | 0.0272 mL | 0.1359 mL | 0.2718 mL | 0.6795 mL | |
| 20 mM | 0.0204 mL | 0.1019 mL | 0.2038 mL | 0.5096 mL | |
| DMSO | 25 mM | 0.0163 mL | 0.0815 mL | 0.1631 mL | 0.4077 mL |
| 30 mM | 0.0136 mL | 0.0679 mL | 0.1359 mL | 0.3397 mL | |
| 40 mM | 0.0102 mL | 0.0510 mL | 0.1019 mL | 0.2548 mL |
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
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