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|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + | 
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| 描述 | HSF1A is an activator of Heat shock transcription factor 1 (HSF1). | 
| Concentration | Treated Time | Description | References | |
| Mouse embryonic fibroblasts (MEFs) | 50 μM | HSF1A provided similar protection against TcdB as observed in HeLa cells | Proc Natl Acad Sci U S A. 2018 Sep 18;115(38):9580-9585 | |
| HeLa cells | 50 μM | 90 minutes | HSF1A blocked TcdB-induced cytotoxicity in a concentration-dependent manner, with 50 μM completely blocking it | Proc Natl Acad Sci U S A. 2018 Sep 18;115(38):9580-9585 | 
| Primary neonatal rat ventricular myocytes (NRVMs) | 10 μM | 24 hours | HSF1A significantly enhanced the ability of CHIP-ΔM/U to inhibit IGF-IIR expression, reduce caspase-3 activation and retained cell viability. | Cell Death Dis. 2016 Nov 3;7(11):e2455 | 
| H9c2 cells | 10 μM | 24 hours | HSF1A significantly inhibited DOX-induced IGF-IIR upregulation, caspase-3 cleavage and caspase-3 activity. | Cell Death Dis. 2016 Nov 3;7(11):e2455 | 
| A549 cells | 200 µM | 4 hours | To evaluate the protective effects of HSF1A against PT-induced cell intoxication in A549 cells. Results showed that HSF1A also effectively reduced PT intoxication in A549 cells. | Toxins (Basel). 2024 Jan 10;16(1):36 | 
| CHO cells | 200 µM | 4 hours | To evaluate the protective effects of HSF1A against PT-induced cell intoxication. Results showed that HSF1A effectively reduced the levels of ADP-ribosylated Gαi in PT-treated cells. | Toxins (Basel). 2024 Jan 10;16(1):36 | 
| Administration | Dosage | Frequency | Description | References | ||
| Wistar Kyoto rats (WKY) | DOX-induced cardiomyopathy model | Intraperitoneal injection | 100 mg/kg/day | Once daily for 6 weeks | HSF1A significantly alleviated DOX-induced cardiac dysfunction and minimized cardiac damage, reducing TUNEL-positive cardiomyocytes. | Cell Death Dis. 2016 Nov 3;7(11):e2455 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.44mL 0.49mL 0.24mL | 12.21mL 2.44mL 1.22mL | 24.42mL 4.88mL 2.44mL | |
| CAS号 | 1196723-93-9 | 
| 分子式 | C21H19N3O2S2 | 
| 分子量 | 409.52 | 
| SMILES Code | O=S(C1=CC=C(CC)C=C1)(NC2=CC(C3=CC=CS3)=NN2C4=CC=CC=C4)=O | 
| MDL No. | MFCD22580417 | 
| 别名 | |
| 运输 | 蓝冰 | 
| InChI Key | KJTITGSAONQVPY-UHFFFAOYSA-N | 
| Pubchem ID | 44472508 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry,2-8°C | 
| 溶解方案 | DMSO: 105 mg/mL(256.39 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
 
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