Cell Meter 比色法MTT细胞增殖检测试剂盒 货号22768-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

Cell Meter 比色法MTT细胞增殖检测试剂盒

Cell Meter 比色法MTT细胞增殖检测试剂盒

货号 22768 存储条件 Multiple
规格 1000 Tests 价格 3732
Ex (nm) Em (nm)
分子量 溶剂
产品详细介绍

简要概述

Cell Meter 检测试剂盒是一套用于检测细胞活力的工具。 Cell Meter 比色法MTT细胞增殖检测试剂盒使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物)定量活细胞的数量。水溶性MTT在代谢活性细胞中产生水不溶性紫色甲瓒。产生的甲瓒的数量与活细胞的数量成正比。在560 nm附近测得吸光度增加。与其他需要繁琐的增溶步骤来溶解不溶于水的甲瓒产物的其他商业MTT测定法不同,Cell Meter 比色MTT细胞增殖试剂盒只需极少的人工操作。我们专有的配方消除了费时的增溶步骤。它是确定细胞增殖和细胞毒性测定中活细胞数量的最强大的MTT试验。检测灵敏度比传统的MTT分析高10倍。

产品说明书

样品分析方案

概述

在96孔板中制备细胞(100 µL /孔)
添加MTT工作溶液(140 µL /孔)
在37°C下孵育2-4小时
读取560 nm处的吸光度

注:使用前,请在室温下解冻所有试剂盒组分。

 

工作溶液制备:

通过将4 mL MTT试剂A(组分A)与10 mL MTT试剂B(组分B)(2:5,MTT试剂A:B的体积比)混合,制备所需的MTT工作溶液量,混匀。

注意:14 mL MTT工作溶液足以在96孔板上进行100次测试。实验前准备足够的MTT工作溶液,并及时使用。

 

操作步骤

1.在具有透明底的组织培养孔板中,培养1000至40,000个细胞/孔。
2.将测试化合物添加到细胞中,并在37°C,5%CO2培养箱中孵育所需的时间(例如24、48或96小时)。3.对于空白孔(不含细胞的培养基),添加相同量的测试化合物。对于96孔板,建议的总体积为100 µL,对于384孔板,建议的总体积为25 µL。
注意:应对每个细胞系进行单独评估,以确定增殖或诱导细胞毒性的最佳细胞密度。对于增殖测定,使用较少的细胞;对于细胞毒性测定,请使用更多的细胞作为开始。
4.向每个孔中加入140 µL /孔(96孔板)或35 µL /孔(384孔板)。
5.在37°C下孵育平板2-4小时,避光。
注意:根据不同的细胞类型和使用的细胞浓度,孵育时间可能从2小时到过夜。优化每个实验的孵育时间。
用吸光度板读数器在OD = 562 nm处检测吸光度。

 

图示

Cell Meter 比色法MTT细胞增殖检测试剂盒   货号22768

图1.用Cell Meter 比色法MTT细胞增殖试剂盒确定细胞数。将0至40,000个细胞/孔/ 100 µL的HeLa细胞添加到透明的底部96孔板中过夜。使用SpectraMax读数器(Molecular Devices)在560nm处检测吸光度。

  

参考文献

Novel Dental Poly (Methyl Methacrylate) Containing Phytoncide for Antifungal Effect and Inhibition of Oral Multispecies Biofilm.
Authors: Lee, Myung-Jin and Kim, Min-Ji and Oh, Sang-Hwan and Kwon, Jae-Sung
Journal: Materials (Basel, Switzerland) (2020)

Toxicity of diuron metabolites in human cells.
Authors: Mohammed, Ali Mustafa and Huovinen, Marjo and Vähäkangas, Kirsi H
Journal: Environmental toxicology and pharmacology (2020): 103409

Biological Effect of Modern Fetal Ultrasound Techniques on Human Dermal Fibroblast Cells.
Authors: M, Morshedi and M, Bakhshandeh and A, Piryaei and A, Emami and M, Zangeneh and A, Razzaghdoust and H, Ghadiri and F, Zayeri
Journal: Journal of biomedical physics & engineering (2019): 335-344

Development and validation of UPLC method for WST-1 cell viability assay and its application to MCTT HCE™ eye irritation test for colorful substances.
Authors: Joo, Kyung-Mi and Kim, Seolyeong and Koo, Ye Ji and Lee, Miri and Lee, Su-Hyun and Choi, Dalwoong and Lim, Kyung-Min
Journal: Toxicology in vitro : an international journal published in association with BIBRA (2019): 412-419

Effects Of Adenosine On Apoptosis Of Ovarian Cancer A2780 Cells Via ROS And Caspase Pathways.
Authors: Xia, Bing and Wang, Jing
Journal: OncoTargets and therapy (2019): 9473-9480

Evaluation of hepatotoxicity potential of a potent traditional Tibetan medicine Zuotai.
Authors: Zhou, Liang-Liang and Chen, Hai-Juan and He, Qiang-Qiang and Li, Cen and Wei, Li-Xin and Shang, Jing
Journal: Journal of ethnopharmacology (2019): 112-118

[Comparative study on quality of decoction pieces of Saposhnikovia divaricata with different growth patterns and years and thinking of standard of decoction pieces of S. divaricata in Chinese Pharmacopoeia].
Authors: Xue, Xue and Wang, Hao and Jia, Tian-Ying and Qu, Wen-Jia and Wang, Hai-Li and Xin, Jie-Ping and Liu, Meng-Nan and Xiong, Hui and Li, Xiang-Ri
Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica (2019): 4034-4042

Colorimetric method for determining viability of sea urchin sperm applied in toxicity tests.
Authors: Resgalla, Charrid and Máximo, Marcus Vinícius and Brasil, Mirella do Nascimento and Pessatti, Marcos Luiz
Journal: Ecotoxicology (London, England) (2018): 499-504

Development of extremely stable dual functionalized gold nanoparticles for effective colorimetric detection of clenbuterol and ractopamine in human urine samples.
Authors: Simon, Turibius and Shellaiah, Muthaiah and Steffi, Perpectual and Sun, Kien Wen and Ko, Fu-Hsiang
Journal: Analytica chimica acta (2018): 96-104

New platinum (II) and palladium (II) complexes of coumarin-thiazole Schiff base with a fluorescent chemosensor properties: Synthesis, spectroscopic characterization, X-ray structure determination, in vitro anticancer activity on various human carcinoma cell lines and computational studies.
Authors: Şahin, Ömer and Özdemir, Ümmühan Özmen and Seferoğlu, Nurgül and Genc, Zuhal Karagöz and Kaya, Kerem and Aydıner, Burcu and Tekin, Suat and Seferoğlu, Zeynel
Journal: Journal of photochemistry and photobiology. B, Biology (2018): 428-439

说明书
Cell Meter 比色法MTT细胞增殖检测试剂盒.pdf

Cell Meter 比色法MTT细胞增殖检测试剂盒 货号22768-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

Cell Meter 比色法MTT细胞增殖检测试剂盒

Cell Meter 比色法MTT细胞增殖检测试剂盒

货号 22768 存储条件 Multiple
规格 1000 Tests 价格 3732
Ex (nm) Em (nm)
分子量 溶剂
产品详细介绍

简要概述

Cell Meter 检测试剂盒是一套用于检测细胞活力的工具。 Cell Meter 比色法MTT细胞增殖检测试剂盒使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物)定量活细胞的数量。水溶性MTT在代谢活性细胞中产生水不溶性紫色甲瓒。产生的甲瓒的数量与活细胞的数量成正比。在560 nm附近测得吸光度增加。与其他需要繁琐的增溶步骤来溶解不溶于水的甲瓒产物的其他商业MTT测定法不同,Cell Meter 比色MTT细胞增殖试剂盒只需极少的人工操作。我们专有的配方消除了费时的增溶步骤。它是确定细胞增殖和细胞毒性测定中活细胞数量的最强大的MTT试验。检测灵敏度比传统的MTT分析高10倍。

产品说明书

样品分析方案

概述

在96孔板中制备细胞(100 µL /孔)
添加MTT工作溶液(140 µL /孔)
在37°C下孵育2-4小时
读取560 nm处的吸光度

注:使用前,请在室温下解冻所有试剂盒组分。

 

工作溶液制备:

通过将4 mL MTT试剂A(组分A)与10 mL MTT试剂B(组分B)(2:5,MTT试剂A:B的体积比)混合,制备所需的MTT工作溶液量,混匀。

注意:14 mL MTT工作溶液足以在96孔板上进行100次测试。实验前准备足够的MTT工作溶液,并及时使用。

 

操作步骤

1.在具有透明底的组织培养孔板中,培养1000至40,000个细胞/孔。
2.将测试化合物添加到细胞中,并在37°C,5%CO2培养箱中孵育所需的时间(例如24、48或96小时)。3.对于空白孔(不含细胞的培养基),添加相同量的测试化合物。对于96孔板,建议的总体积为100 µL,对于384孔板,建议的总体积为25 µL。
注意:应对每个细胞系进行单独评估,以确定增殖或诱导细胞毒性的最佳细胞密度。对于增殖测定,使用较少的细胞;对于细胞毒性测定,请使用更多的细胞作为开始。
4.向每个孔中加入140 µL /孔(96孔板)或35 µL /孔(384孔板)。
5.在37°C下孵育平板2-4小时,避光。
注意:根据不同的细胞类型和使用的细胞浓度,孵育时间可能从2小时到过夜。优化每个实验的孵育时间。
用吸光度板读数器在OD = 562 nm处检测吸光度。

 

图示

Cell Meter 比色法MTT细胞增殖检测试剂盒   货号22768

图1.用Cell Meter 比色法MTT细胞增殖试剂盒确定细胞数。将0至40,000个细胞/孔/ 100 µL的HeLa细胞添加到透明的底部96孔板中过夜。使用SpectraMax读数器(Molecular Devices)在560nm处检测吸光度。

  

参考文献

Novel Dental Poly (Methyl Methacrylate) Containing Phytoncide for Antifungal Effect and Inhibition of Oral Multispecies Biofilm.
Authors: Lee, Myung-Jin and Kim, Min-Ji and Oh, Sang-Hwan and Kwon, Jae-Sung
Journal: Materials (Basel, Switzerland) (2020)

Toxicity of diuron metabolites in human cells.
Authors: Mohammed, Ali Mustafa and Huovinen, Marjo and Vähäkangas, Kirsi H
Journal: Environmental toxicology and pharmacology (2020): 103409

Biological Effect of Modern Fetal Ultrasound Techniques on Human Dermal Fibroblast Cells.
Authors: M, Morshedi and M, Bakhshandeh and A, Piryaei and A, Emami and M, Zangeneh and A, Razzaghdoust and H, Ghadiri and F, Zayeri
Journal: Journal of biomedical physics & engineering (2019): 335-344

Development and validation of UPLC method for WST-1 cell viability assay and its application to MCTT HCE™ eye irritation test for colorful substances.
Authors: Joo, Kyung-Mi and Kim, Seolyeong and Koo, Ye Ji and Lee, Miri and Lee, Su-Hyun and Choi, Dalwoong and Lim, Kyung-Min
Journal: Toxicology in vitro : an international journal published in association with BIBRA (2019): 412-419

Effects Of Adenosine On Apoptosis Of Ovarian Cancer A2780 Cells Via ROS And Caspase Pathways.
Authors: Xia, Bing and Wang, Jing
Journal: OncoTargets and therapy (2019): 9473-9480

Evaluation of hepatotoxicity potential of a potent traditional Tibetan medicine Zuotai.
Authors: Zhou, Liang-Liang and Chen, Hai-Juan and He, Qiang-Qiang and Li, Cen and Wei, Li-Xin and Shang, Jing
Journal: Journal of ethnopharmacology (2019): 112-118

[Comparative study on quality of decoction pieces of Saposhnikovia divaricata with different growth patterns and years and thinking of standard of decoction pieces of S. divaricata in Chinese Pharmacopoeia].
Authors: Xue, Xue and Wang, Hao and Jia, Tian-Ying and Qu, Wen-Jia and Wang, Hai-Li and Xin, Jie-Ping and Liu, Meng-Nan and Xiong, Hui and Li, Xiang-Ri
Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica (2019): 4034-4042

Colorimetric method for determining viability of sea urchin sperm applied in toxicity tests.
Authors: Resgalla, Charrid and Máximo, Marcus Vinícius and Brasil, Mirella do Nascimento and Pessatti, Marcos Luiz
Journal: Ecotoxicology (London, England) (2018): 499-504

Development of extremely stable dual functionalized gold nanoparticles for effective colorimetric detection of clenbuterol and ractopamine in human urine samples.
Authors: Simon, Turibius and Shellaiah, Muthaiah and Steffi, Perpectual and Sun, Kien Wen and Ko, Fu-Hsiang
Journal: Analytica chimica acta (2018): 96-104

New platinum (II) and palladium (II) complexes of coumarin-thiazole Schiff base with a fluorescent chemosensor properties: Synthesis, spectroscopic characterization, X-ray structure determination, in vitro anticancer activity on various human carcinoma cell lines and computational studies.
Authors: Şahin, Ömer and Özdemir, Ümmühan Özmen and Seferoğlu, Nurgül and Genc, Zuhal Karagöz and Kaya, Kerem and Aydıner, Burcu and Tekin, Suat and Seferoğlu, Zeynel
Journal: Journal of photochemistry and photobiology. B, Biology (2018): 428-439

说明书
Cell Meter 比色法MTT细胞增殖检测试剂盒.pdf

Cell Meter 比色法MTT细胞增殖检测试剂盒 货号22769-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

Cell Meter 比色法MTT细胞增殖检测试剂盒

Cell Meter 比色法MTT细胞增殖检测试剂盒

货号 22769 存储条件 Multiple
规格 5000 Tests 价格 9468
Ex (nm) Em (nm)
分子量 溶剂
产品详细介绍

简要概述

Cell Meter 检测试剂盒是一套用于检测细胞活力的工具。 Cell Meter 比色法MTT细胞增殖检测试剂盒使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物)定量活细胞的数量。水溶性MTT在代谢活性细胞中产生水不溶性紫色甲瓒。产生的甲瓒的数量与活细胞的数量成正比。在560 nm附近测得吸光度增加。与其他需要繁琐的增溶步骤来溶解不溶于水的甲瓒产物的其他商业MTT测定法不同,Cell Meter 比色MTT细胞增殖试剂盒只需极少的人工操作。我们专有的配方消除了费时的增溶步骤。它是确定细胞增殖和细胞毒性测定中活细胞数量的最强大的MTT试验。检测灵敏度比传统的MTT分析高10倍。

产品说明书

样品分析方案

概述

在96孔板中制备细胞(100 µL /孔)
添加MTT工作溶液(140 µL /孔)
在37°C下孵育2-4小时
读取560 nm处的吸光度

注:使用前,请在室温下解冻所有试剂盒组分。

 

工作溶液制备:

通过将4 mL MTT试剂A(组分A)与10 mL MTT试剂B(组分B)(2:5,MTT试剂A:B的体积比)混合,制备所需的MTT工作溶液量,混匀。

注意:14 mL MTT工作溶液足以在96孔板上进行100次测试。实验前准备足够的MTT工作溶液,并及时使用。

 

操作步骤

1.在具有透明底的组织培养孔板中,培养1000至40,000个细胞/孔。
2.将测试化合物添加到细胞中,并在37°C,5%CO2培养箱中孵育所需的时间(例如24、48或96小时)。3.对于空白孔(不含细胞的培养基),添加相同量的测试化合物。对于96孔板,建议的总体积为100 µL,对于384孔板,建议的总体积为25 µL。
注意:应对每个细胞系进行单独评估,以确定增殖或诱导细胞毒性的最佳细胞密度。对于增殖测定,使用较少的细胞;对于细胞毒性测定,请使用更多的细胞作为开始。
4.向每个孔中加入140 µL /孔(96孔板)或35 µL /孔(384孔板)。
5.在37°C下孵育平板2-4小时,避光。
注意:根据不同的细胞类型和使用的细胞浓度,孵育时间可能从2小时到过夜。优化每个实验的孵育时间。
用吸光度板读数器在OD = 562 nm处检测吸光度。

 

图示

Cell Meter 比色法MTT细胞增殖检测试剂盒   货号22769

图1.用Cell Meter 比色法MTT细胞增殖试剂盒确定细胞数。将0至40,000个细胞/孔/ 100 µL的HeLa细胞添加到透明的底部96孔板中过夜。使用SpectraMax读数器(Molecular Devices)在560nm处检测吸光度。

  

参考文献

Novel Dental Poly (Methyl Methacrylate) Containing Phytoncide for Antifungal Effect and Inhibition of Oral Multispecies Biofilm.
Authors: Lee, Myung-Jin and Kim, Min-Ji and Oh, Sang-Hwan and Kwon, Jae-Sung
Journal: Materials (Basel, Switzerland) (2020)

Toxicity of diuron metabolites in human cells.
Authors: Mohammed, Ali Mustafa and Huovinen, Marjo and Vähäkangas, Kirsi H
Journal: Environmental toxicology and pharmacology (2020): 103409

Biological Effect of Modern Fetal Ultrasound Techniques on Human Dermal Fibroblast Cells.
Authors: M, Morshedi and M, Bakhshandeh and A, Piryaei and A, Emami and M, Zangeneh and A, Razzaghdoust and H, Ghadiri and F, Zayeri
Journal: Journal of biomedical physics & engineering (2019): 335-344

Development and validation of UPLC method for WST-1 cell viability assay and its application to MCTT HCE™ eye irritation test for colorful substances.
Authors: Joo, Kyung-Mi and Kim, Seolyeong and Koo, Ye Ji and Lee, Miri and Lee, Su-Hyun and Choi, Dalwoong and Lim, Kyung-Min
Journal: Toxicology in vitro : an international journal published in association with BIBRA (2019): 412-419

Effects Of Adenosine On Apoptosis Of Ovarian Cancer A2780 Cells Via ROS And Caspase Pathways.
Authors: Xia, Bing and Wang, Jing
Journal: OncoTargets and therapy (2019): 9473-9480

Evaluation of hepatotoxicity potential of a potent traditional Tibetan medicine Zuotai.
Authors: Zhou, Liang-Liang and Chen, Hai-Juan and He, Qiang-Qiang and Li, Cen and Wei, Li-Xin and Shang, Jing
Journal: Journal of ethnopharmacology (2019): 112-118

[Comparative study on quality of decoction pieces of Saposhnikovia divaricata with different growth patterns and years and thinking of standard of decoction pieces of S. divaricata in Chinese Pharmacopoeia].
Authors: Xue, Xue and Wang, Hao and Jia, Tian-Ying and Qu, Wen-Jia and Wang, Hai-Li and Xin, Jie-Ping and Liu, Meng-Nan and Xiong, Hui and Li, Xiang-Ri
Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica (2019): 4034-4042

Colorimetric method for determining viability of sea urchin sperm applied in toxicity tests.
Authors: Resgalla, Charrid and Máximo, Marcus Vinícius and Brasil, Mirella do Nascimento and Pessatti, Marcos Luiz
Journal: Ecotoxicology (London, England) (2018): 499-504

Development of extremely stable dual functionalized gold nanoparticles for effective colorimetric detection of clenbuterol and ractopamine in human urine samples.
Authors: Simon, Turibius and Shellaiah, Muthaiah and Steffi, Perpectual and Sun, Kien Wen and Ko, Fu-Hsiang
Journal: Analytica chimica acta (2018): 96-104

New platinum (II) and palladium (II) complexes of coumarin-thiazole Schiff base with a fluorescent chemosensor properties: Synthesis, spectroscopic characterization, X-ray structure determination, in vitro anticancer activity on various human carcinoma cell lines and computational studies.
Authors: Şahin, Ömer and Özdemir, Ümmühan Özmen and Seferoğlu, Nurgül and Genc, Zuhal Karagöz and Kaya, Kerem and Aydıner, Burcu and Tekin, Suat and Seferoğlu, Zeynel
Journal: Journal of photochemistry and photobiology. B, Biology (2018): 428-439

说明书
Cell Meter 比色法MTT细胞增殖检测试剂盒.pdf

Cell Meter 比色法MTT细胞增殖检测试剂盒 货号22769-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

Cell Meter 比色法MTT细胞增殖检测试剂盒

Cell Meter 比色法MTT细胞增殖检测试剂盒

货号 22769 存储条件 Multiple
规格 5000 Tests 价格 9468
Ex (nm) Em (nm)
分子量 溶剂
产品详细介绍

简要概述

Cell Meter 检测试剂盒是一套用于检测细胞活力的工具。 Cell Meter 比色法MTT细胞增殖检测试剂盒使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物)定量活细胞的数量。水溶性MTT在代谢活性细胞中产生水不溶性紫色甲瓒。产生的甲瓒的数量与活细胞的数量成正比。在560 nm附近测得吸光度增加。与其他需要繁琐的增溶步骤来溶解不溶于水的甲瓒产物的其他商业MTT测定法不同,Cell Meter 比色MTT细胞增殖试剂盒只需极少的人工操作。我们专有的配方消除了费时的增溶步骤。它是确定细胞增殖和细胞毒性测定中活细胞数量的最强大的MTT试验。检测灵敏度比传统的MTT分析高10倍。

产品说明书

样品分析方案

概述

在96孔板中制备细胞(100 µL /孔)
添加MTT工作溶液(140 µL /孔)
在37°C下孵育2-4小时
读取560 nm处的吸光度

注:使用前,请在室温下解冻所有试剂盒组分。

 

工作溶液制备:

通过将4 mL MTT试剂A(组分A)与10 mL MTT试剂B(组分B)(2:5,MTT试剂A:B的体积比)混合,制备所需的MTT工作溶液量,混匀。

注意:14 mL MTT工作溶液足以在96孔板上进行100次测试。实验前准备足够的MTT工作溶液,并及时使用。

 

操作步骤

1.在具有透明底的组织培养孔板中,培养1000至40,000个细胞/孔。
2.将测试化合物添加到细胞中,并在37°C,5%CO2培养箱中孵育所需的时间(例如24、48或96小时)。3.对于空白孔(不含细胞的培养基),添加相同量的测试化合物。对于96孔板,建议的总体积为100 µL,对于384孔板,建议的总体积为25 µL。
注意:应对每个细胞系进行单独评估,以确定增殖或诱导细胞毒性的最佳细胞密度。对于增殖测定,使用较少的细胞;对于细胞毒性测定,请使用更多的细胞作为开始。
4.向每个孔中加入140 µL /孔(96孔板)或35 µL /孔(384孔板)。
5.在37°C下孵育平板2-4小时,避光。
注意:根据不同的细胞类型和使用的细胞浓度,孵育时间可能从2小时到过夜。优化每个实验的孵育时间。
用吸光度板读数器在OD = 562 nm处检测吸光度。

 

图示

Cell Meter 比色法MTT细胞增殖检测试剂盒   货号22769

图1.用Cell Meter 比色法MTT细胞增殖试剂盒确定细胞数。将0至40,000个细胞/孔/ 100 µL的HeLa细胞添加到透明的底部96孔板中过夜。使用SpectraMax读数器(Molecular Devices)在560nm处检测吸光度。

  

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说明书
Cell Meter 比色法MTT细胞增殖检测试剂盒.pdf