| 生物活性： |
背景说明：MTT是一种广泛用于测量细胞增殖的比色剂。
生物活性：MTT是一种广泛用于测量细胞增殖的比色剂。 MTT在活细胞中从黄色还原为紫色。
In Vitro：MTT与罗丹明B联合使用以测量线粒体膜电位。 MTT-formazan在线粒体中产生，作为罗丹明的荧光猝灭剂，根据膜电位分布在活细胞膜上。在没有mPMS的情况下，MTT的细胞减少很强。当MTT掺入大的单层脂质体中时，它是不透膜的，因此它通过内吞作用被细胞摄取[1]。
数据来源文献：[1]. Berridge MV， et al. Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction. Biotechnol Annu Rev. 2005;11:127-52.
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| 其它标识： |
EC：EINECS 206-069-5
MDL：MFCD00011964
SMILES：CC1=C(C)N=C(N2N=C(C3=CC=CC=C3)N=[N+]2C4=CC=CC=C4)S1.[Br-]
InChIKey：AZKSAVLVSZKNRD-UHFFFAOYSA-M
InChI：InChI=1S/C18H16N5S.BrH/c1-13-14(2)24-18(19-13)23-21-17(15-9-5-3-6-10-15)20-22(23)16-11-7-4-8-12-16;/h3-12H,1-2H3;1H/q+1;/p-1
PubChem CID：64965
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| 基本信息： |
CAS：298-93-1
中文名称：噻唑蓝
英文名称：MTT
别名：Thiazolyl Blue;Thiazolyl Blue Tetrazolium bromide;Methylthiazolyldiphenyl-tetrazolium bromide;3-(4, 5-Dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide
分子式：C18H16BrN5S
分子量：414.32
规格：10mM*1mL in Water ; 10mM*1mL in DMSO ; 5mg/mL*1mL in Water ; 1g ; 200mg ; 500mg
溶解性：Soluble in Water/DMSO
纯度：≥98%
外观(性状)：Light yellow to yellow Solid
储存条件：Powder:2-8℃，2 years;Insolvent(母液):-20℃，6 months;-80℃，1 year
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产品详情
MTT是一种广泛用于测量细胞增殖的比色剂。MTT可以被线粒体内的一些脱氢酶还原生成结晶状的深紫色产物formazan，可以被DMSO完全溶解，然后通过酶标仪可以测定490nm波长附近的吸光度。细胞增殖越多越快，则吸光度越高；细胞毒性越大，则吸光度越低。
注意事项：MTT溶液需避光保存，长时间光照会导致失效。当颜色变为灰绿色时，请勿使用。
使用说明（仅供参考）
1.收集对数期细胞，根据自己的实验需求，培养细胞。
2.小心吸去上清，加入90μL新鲜培养基，再加入10μL MTT溶液，继续培养4 h。
3.然后吸掉上清，每孔加入110μL DMSO，置摇床上低速振荡10 min，使结晶物充分溶解。
4.在酶联免疫检测仪490 nm处测量各孔的吸光值。
注：MTT溶液浓度一般的常用浓度为0.5%（仅供参考），实验者也可根据自己的实验需求进行调整。
使用本产品的应用案例（仅供参考）
In Vitro
Cell （HEK-293 cells，37 °C ，4 h，490nm）
Cell viability was determined by a quantitative colorimetric assay with MTT. To screen the pre-protection of SDAP1 and SDAP2, cells were pretreated with SDAP1 and SDAP2 (0.25, 0.5, 0.75, 1, 1.25, 1.5 mg/mL) before administration of GM (3 mg/mL) for 24 h. HEK-293 cells were dispensed in 96-well plates at a density of 8,000 cells/well and cultured at 37 °C for 24 h. Afer 24 h incubation, cells were treated with various concentrations of SDAP1 and SDAP2 (0.25, 0.5, 0.75, 1, 1.25 and 1 mg/mL) at 24 h, and aferwards exposed to GM (3 mg/mL) for 24 h. Next, afer 24 h of GM treatment, the MTT solution was added to each well, and incubated at 37 °C for 4 h. Te medium was removed, and 150 μL of dimethylsulfoxide (Solarbio, China) was added to each well. Finally, the optical density was detected with a microplate reader at 490 nm.
来源文献：Wang Z, Wang L, Wang J, Luo J, Ruan H, Zhang J. Purified Sika deer antler protein attenuates GM-induced nephrotoxicity by activating Nrf2 pathway and inhibiting NF-κB pathway. Sci Rep. 2020 Sep 24;10(1):15601. doi: 10.1038/s41598-020-71943-6. PMID: 32973191; PMCID: PMC7518274.
Cell（HepG2 Cell，5 mg/mL MTT，4h, 570nm）
Methylthiazole tetrazolium (MTT) assay was applied to measure the cell viability of Up-3, Up-4, and Up-5. Briefly, after incubation, the cells was washed with PBS, and incubated with 10 µL of MTT (5 mg/mL) for 4 hours. The supernatants was mixed with 100 µL of DMSO and then the absorbance was measured at 570 nm with a microplate reader. The absorbance of the untreated cells (Normal group) was considered as 100%.
来源文献：Zhong QW, Zhou TS, Qiu WH, Wang YK, Xu QL, Ke SZ, Wang SJ, Jin WH, Chen JW, Zhang HW, Wei B, Wang H. Characterization and hypoglycemic effects of sulfated polysaccharides derived from brown seaweed Undaria pinnatifida. Food Chem. 2021 Mar 30;341(Pt 1):128148. doi: 10.1016/j.foodchem.2020.128148. Epub 2020 Sep 22. PMID: 33038776.
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