适用仪器

样品实验方案

简要概述

1. 在生长培养基中准备细胞
2. 添加Calbryte 590 AM染料加载溶液（对于96孔板为100 µL /孔，对于384孔板为25 µL /孔）
3. 在室温或37°C下孵育45-60分钟
4. 在Ex / Em = 540/590 nm处检测荧光

溶液配制

储备溶液配制

1. Calbryte 590 AM储备溶液：向Calbryte 590 AM（组分A）的小瓶中加入20 µL（#36200）或200 µL（#36201和＃36202）DMSO。 注意：20 µL Calbryte 590 AM储备溶液足以装一板。 未用完的Calbryte 590 AM储备溶液可以等分分装，并在<-20℃下保存。 注意：避光，并避免重复的冻融循环。

2.分析缓冲液（1X）：将9 mL的HHBS（组分C，试剂盒#36202中未包括）与1 mL的10XPluronic®F127 Plus（10X）（组分B）充分混合。

工作溶液配制

Calbryte 590 AM工作溶液：将20 µL Calbryte 590 AM储备溶液添加到10 mL的测定缓冲液（1X）中，并充分混合。 注意：该工作溶液在室温下至少可稳定2小时。 注意：10 mL染料加载溶液足以用于一块96孔板。

实验步骤

1.将100 µL /孔（96孔板）或25 µL /孔（384孔板）的Calbryte 590 AM染料加载溶液添加到细胞板中。

2.在细胞培养箱中将染料加载板孵育60分钟，然后在室温下将板再孵育15-30分钟。 注意：如果测定需要37°C，请立即进行实验，而无需进一步室温孵育。 如果细胞在室温下能长时间正常工作，则在室温下孵育细胞板1小时（建议孵育时间不超过2小时）。

3.用HHBS或所需的缓冲液准备复合板。

4.通过检测Ex / Em = 540/590 nm的荧光强度。

图示

图1.图表说明了信噪比（SNR）x 100％。 使用Screen Quest Calbryte 590无丙磺舒和无洗涤钙测定试剂盒测量CHO-K1细胞中的ATP剂量反应。 将CHO-K1细胞以50,000个细胞/ 100 µL /孔在96孔黑色板上接种过夜。 加入100 µL的染料加载溶液，在37°C下孵育45分钟，在室温下孵育15分钟。 FlexStation 3添加了ATP（50 µL /孔）以达到最终指示的浓度。

相关产品

Calreticulin regulates TGF-β1-induced epithelial mesenchymal transition through modulating Smad signaling and calcium signaling
Authors: Wu, Yanjiao and Xu, Xiaoli and Ma, Lunkun and Yi, Qian and Sun, Weichao and Tang, Liling
Journal: The International Journal of Biochemistry & Cell Biology (2017)

Dexmedetomidine reduces hypoxia/reoxygenation injury by regulating mitochondrial fission in rat hippocampal neurons
Authors: Liu, Jia and Du, Qing and Zhu, He and Li, Yu and Liu, Maodong and Yu, Shoushui and Wang, Shilei
Journal: Int J Clin Exp Med (2017): 6861–6868

Monosialoganglioside 1 may alleviate neurotoxicity induced by propofol combined with remifentanil in neural stem cells
Authors: Lu, Jiang and Yao, Xue-qin and Luo, Xin and Wang, Yu and Chung, Sookja Kim and Tang, He-xin and Cheung, Chi Wai and Wang, Xian-yu and Meng, Chen and Li, Qing and others
Journal: Neural Regeneration Research (2017): 945

Obtaining spontaneously beating cardiomyocyte-like cells from adipose-derived stromal vascular fractions cultured on enzyme-crosslinked gelatin hydrogels
Authors: Yang, Gang and Xiao, Zhenghua and Ren, Xiaomei and Long, Haiyan and Ma, Kunlong and Qian, Hong and Guo, Yingqiang
Journal: Scientific Reports (2017): 41781

Di (2-ethylhexyl) phthalate-induced apoptosis in rat INS-1 cells is dependent on activation of endoplasmic reticulum stress and suppression of antioxidant protection
Authors: Sun, Xia and Lin, Yi and Huang, Qiansheng and Shi, Junpeng and Qiu, Ling and Kang, Mei and Chen, Yajie and Fang, Chao and Ye, Ting and Dong, Sijun
Journal: Journal of cellular and molecular medicine (2015): 581–594

The effect of mitochondrial calcium uniporter on mitochondrial fission in hippocampus cells ischemia/reperfusion injury
Authors: Zhao, Lantao and Li, Shuhong and Wang, Shilei and Yu, Ning and Liu, Jia
Journal: Biochemical and biophysical research communications (2015): 537–542

Fungus induces the release of IL-8 in human corneal epithelial cells, via Dectin-1-mediated protein kinase C pathways.
Authors: Peng, Xu-Dong and Zhao, Gui-Qiu and Lin, Jing and Jiang, Nan and Xu, Qiang and Zhu, Cheng-Cheng and Qu, Jain-Qiu and Cong, Lin and Li, Hui
Journal: International journal of ophthalmology (2014): 441–447

Propofol and remifentanil at moderate and high concentrations affect proliferation and differentiation of neural stem/progenitor cells
Authors: Li, Qing and Lu, Jiang and Wang, Xianyu and others
Journal: Neural regeneration research (2014): 2002

Role of mitochondrial calcium uniporter in regulating mitochondrial fission in the cerebral cortexes of living rats
Authors: Liang, Nan and Wang, Peng and Wang, Shilei and Li, Shuhong and Li, Yu and Wang, Jinying and Wang, Min
Journal: Journal of Neural Transmission (2014): 593–600

Increased expression of cell adhesion molecule 1 by mast cells as a cause of enhanced nerve–mast cell interaction in a hapten-induced mouse model of atopic dermatitis
Authors: Hagiyama, M and Inoue, T and Furuno, T and Iino, T and Itami, S and Nakanishi, M and Asada, H and Hosokawa, Y and Ito, A
Journal: British Journal of Dermatology (2013): 771–778

点击查看光谱

适用仪器

样品实验方案

简要概述

1. 在生长培养基中准备细胞
2. 添加Calbryte 590 AM染料加载溶液（对于96孔板为100 µL /孔，对于384孔板为25 µL /孔）
3. 在室温或37°C下孵育45-60分钟
4. 在Ex / Em = 540/590 nm处检测荧光

溶液配制

储备溶液配制

1. Calbryte 590 AM储备溶液：向Calbryte 590 AM（组分A）的小瓶中加入20 µL（#36200）或200 µL（#36201和＃36202）DMSO。 注意：20 µL Calbryte 590 AM储备溶液足以装一板。 未用完的Calbryte 590 AM储备溶液可以等分分装，并在<-20℃下保存。 注意：避光，并避免重复的冻融循环。

2.分析缓冲液（1X）：将9 mL的HHBS（组分C，试剂盒#36202中未包括）与1 mL的10XPluronic®F127 Plus（10X）（组分B）充分混合。

工作溶液配制

Calbryte 590 AM工作溶液：将20 µL Calbryte 590 AM储备溶液添加到10 mL的测定缓冲液（1X）中，并充分混合。 注意：该工作溶液在室温下至少可稳定2小时。 注意：10 mL染料加载溶液足以用于一块96孔板。

实验步骤

1.将100 µL /孔（96孔板）或25 µL /孔（384孔板）的Calbryte 590 AM染料加载溶液添加到细胞板中。

2.在细胞培养箱中将染料加载板孵育60分钟，然后在室温下将板再孵育15-30分钟。 注意：如果测定需要37°C，请立即进行实验，而无需进一步室温孵育。 如果细胞在室温下能长时间正常工作，则在室温下孵育细胞板1小时（建议孵育时间不超过2小时）。

3.用HHBS或所需的缓冲液准备复合板。

4.通过检测Ex / Em = 540/590 nm的荧光强度。
 

图示

图1.图表说明了信噪比（SNR）x 100％。 使用Screen Quest Calbryte 590无丙磺舒和无洗涤钙测定试剂盒测量CHO-K1细胞中的ATP剂量反应。 将CHO-K1细胞以50,000个细胞/ 100 µL /孔在96孔黑色板上接种过夜。 加入100 µL的染料加载溶液，在37°C下孵育45分钟，在室温下孵育15分钟。 FlexStation 3添加了ATP（50 µL /孔）以达到最终指示的浓度。

相关产品

Calreticulin regulates TGF-β1-induced epithelial mesenchymal transition through modulating Smad signaling and calcium signaling
Authors: Wu, Yanjiao and Xu, Xiaoli and Ma, Lunkun and Yi, Qian and Sun, Weichao and Tang, Liling
Journal: The International Journal of Biochemistry & Cell Biology (2017)

Dexmedetomidine reduces hypoxia/reoxygenation injury by regulating mitochondrial fission in rat hippocampal neurons
Authors: Liu, Jia and Du, Qing and Zhu, He and Li, Yu and Liu, Maodong and Yu, Shoushui and Wang, Shilei
Journal: Int J Clin Exp Med (2017): 6861–6868

Monosialoganglioside 1 may alleviate neurotoxicity induced by propofol combined with remifentanil in neural stem cells
Authors: Lu, Jiang and Yao, Xue-qin and Luo, Xin and Wang, Yu and Chung, Sookja Kim and Tang, He-xin and Cheung, Chi Wai and Wang, Xian-yu and Meng, Chen and Li, Qing and others
Journal: Neural Regeneration Research (2017): 945

Obtaining spontaneously beating cardiomyocyte-like cells from adipose-derived stromal vascular fractions cultured on enzyme-crosslinked gelatin hydrogels
Authors: Yang, Gang and Xiao, Zhenghua and Ren, Xiaomei and Long, Haiyan and Ma, Kunlong and Qian, Hong and Guo, Yingqiang
Journal: Scientific Reports (2017): 41781

Di (2-ethylhexyl) phthalate-induced apoptosis in rat INS-1 cells is dependent on activation of endoplasmic reticulum stress and suppression of antioxidant protection
Authors: Sun, Xia and Lin, Yi and Huang, Qiansheng and Shi, Junpeng and Qiu, Ling and Kang, Mei and Chen, Yajie and Fang, Chao and Ye, Ting and Dong, Sijun
Journal: Journal of cellular and molecular medicine (2015): 581–594

The effect of mitochondrial calcium uniporter on mitochondrial fission in hippocampus cells ischemia/reperfusion injury
Authors: Zhao, Lantao and Li, Shuhong and Wang, Shilei and Yu, Ning and Liu, Jia
Journal: Biochemical and biophysical research communications (2015): 537–542

Fungus induces the release of IL-8 in human corneal epithelial cells, via Dectin-1-mediated protein kinase C pathways.
Authors: Peng, Xu-Dong and Zhao, Gui-Qiu and Lin, Jing and Jiang, Nan and Xu, Qiang and Zhu, Cheng-Cheng and Qu, Jain-Qiu and Cong, Lin and Li, Hui
Journal: International journal of ophthalmology (2014): 441–447

Propofol and remifentanil at moderate and high concentrations affect proliferation and differentiation of neural stem/progenitor cells
Authors: Li, Qing and Lu, Jiang and Wang, Xianyu and others
Journal: Neural regeneration research (2014): 2002

Role of mitochondrial calcium uniporter in regulating mitochondrial fission in the cerebral cortexes of living rats
Authors: Liang, Nan and Wang, Peng and Wang, Shilei and Li, Shuhong and Li, Yu and Wang, Jinying and Wang, Min
Journal: Journal of Neural Transmission (2014): 593–600

Increased expression of cell adhesion molecule 1 by mast cells as a cause of enhanced nerve–mast cell interaction in a hapten-induced mouse model of atopic dermatitis
Authors: Hagiyama, M and Inoue, T and Furuno, T and Iino, T and Itami, S and Nakanishi, M and Asada, H and Hosokawa, Y and Ito, A
Journal: British Journal of Dermatology (2013): 771–778

点击查看光谱

适用仪器

样品实验方案

简要概述

1. 在生长培养基中准备细胞
2. 添加Calbryte 590 AM染料加载溶液（对于96孔板为100 µL /孔，对于384孔板为25 µL /孔）
3. 在室温或37°C下孵育45-60分钟
4. 在Ex / Em = 540/590 nm处检测荧光

溶液配制

储备溶液配制

1. Calbryte 590 AM储备溶液：向Calbryte 590 AM（组分A）的小瓶中加入20 µL（#36200）或200 µL（#36201和＃36202）DMSO。 注意：20 µL Calbryte 590 AM储备溶液足以装一板。 未用完的Calbryte 590 AM储备溶液可以等分分装，并在<-20℃下保存。 注意：避光，并避免重复的冻融循环。

2.分析缓冲液（1X）：将9 mL的HHBS（组分C，试剂盒#36202中未包括）与1 mL的10XPluronic®F127 Plus（10X）（组分B）充分混合。

工作溶液配制

Calbryte 590 AM工作溶液：将20 µL Calbryte 590 AM储备溶液添加到10 mL的测定缓冲液（1X）中，并充分混合。 注意：该工作溶液在室温下至少可稳定2小时。 注意：10 mL染料加载溶液足以用于一块96孔板。

实验步骤

1.将100 µL /孔（96孔板）或25 µL /孔（384孔板）的Calbryte 590 AM染料加载溶液添加到细胞板中。

2.在细胞培养箱中将染料加载板孵育60分钟，然后在室温下将板再孵育15-30分钟。 注意：如果测定需要37°C，请立即进行实验，而无需进一步室温孵育。 如果细胞在室温下能长时间正常工作，则在室温下孵育细胞板1小时（建议孵育时间不超过2小时）。

3.用HHBS或所需的缓冲液准备复合板。

4.通过检测Ex / Em = 540/590 nm的荧光强度。

图示

图1.图表说明了信噪比（SNR）x 100％。 使用Screen Quest Calbryte 590无丙磺舒和无洗涤钙测定试剂盒测量CHO-K1细胞中的ATP剂量反应。 将CHO-K1细胞以50,000个细胞/ 100 µL /孔在96孔黑色板上接种过夜。 加入100 µL的染料加载溶液，在37°C下孵育45分钟，在室温下孵育15分钟。 FlexStation 3添加了ATP（50 µL /孔）以达到最终指示的浓度。

相关产品

Calreticulin regulates TGF-β1-induced epithelial mesenchymal transition through modulating Smad signaling and calcium signaling
Authors: Wu, Yanjiao and Xu, Xiaoli and Ma, Lunkun and Yi, Qian and Sun, Weichao and Tang, Liling
Journal: The International Journal of Biochemistry & Cell Biology (2017)

Dexmedetomidine reduces hypoxia/reoxygenation injury by regulating mitochondrial fission in rat hippocampal neurons
Authors: Liu, Jia and Du, Qing and Zhu, He and Li, Yu and Liu, Maodong and Yu, Shoushui and Wang, Shilei
Journal: Int J Clin Exp Med (2017): 6861–6868

Monosialoganglioside 1 may alleviate neurotoxicity induced by propofol combined with remifentanil in neural stem cells
Authors: Lu, Jiang and Yao, Xue-qin and Luo, Xin and Wang, Yu and Chung, Sookja Kim and Tang, He-xin and Cheung, Chi Wai and Wang, Xian-yu and Meng, Chen and Li, Qing and others
Journal: Neural Regeneration Research (2017): 945

Obtaining spontaneously beating cardiomyocyte-like cells from adipose-derived stromal vascular fractions cultured on enzyme-crosslinked gelatin hydrogels
Authors: Yang, Gang and Xiao, Zhenghua and Ren, Xiaomei and Long, Haiyan and Ma, Kunlong and Qian, Hong and Guo, Yingqiang
Journal: Scientific Reports (2017): 41781

Di (2-ethylhexyl) phthalate-induced apoptosis in rat INS-1 cells is dependent on activation of endoplasmic reticulum stress and suppression of antioxidant protection
Authors: Sun, Xia and Lin, Yi and Huang, Qiansheng and Shi, Junpeng and Qiu, Ling and Kang, Mei and Chen, Yajie and Fang, Chao and Ye, Ting and Dong, Sijun
Journal: Journal of cellular and molecular medicine (2015): 581–594

The effect of mitochondrial calcium uniporter on mitochondrial fission in hippocampus cells ischemia/reperfusion injury
Authors: Zhao, Lantao and Li, Shuhong and Wang, Shilei and Yu, Ning and Liu, Jia
Journal: Biochemical and biophysical research communications (2015): 537–542

Fungus induces the release of IL-8 in human corneal epithelial cells, via Dectin-1-mediated protein kinase C pathways.
Authors: Peng, Xu-Dong and Zhao, Gui-Qiu and Lin, Jing and Jiang, Nan and Xu, Qiang and Zhu, Cheng-Cheng and Qu, Jain-Qiu and Cong, Lin and Li, Hui
Journal: International journal of ophthalmology (2014): 441–447

Propofol and remifentanil at moderate and high concentrations affect proliferation and differentiation of neural stem/progenitor cells
Authors: Li, Qing and Lu, Jiang and Wang, Xianyu and others
Journal: Neural regeneration research (2014): 2002

Role of mitochondrial calcium uniporter in regulating mitochondrial fission in the cerebral cortexes of living rats
Authors: Liang, Nan and Wang, Peng and Wang, Shilei and Li, Shuhong and Li, Yu and Wang, Jinying and Wang, Min
Journal: Journal of Neural Transmission (2014): 593–600

Increased expression of cell adhesion molecule 1 by mast cells as a cause of enhanced nerve–mast cell interaction in a hapten-induced mouse model of atopic dermatitis
Authors: Hagiyama, M and Inoue, T and Furuno, T and Iino, T and Itami, S and Nakanishi, M and Asada, H and Hosokawa, Y and Ito, A
Journal: British Journal of Dermatology (2013): 771–778

适用仪器

Screen Quest Fluo-8钙检测试剂盒是美国AAT Bioquest生产的钙检测试剂盒，钙通量测定是用于筛选G蛋白偶联受体（GPCR）的药物发现中的优选方法。 Screen Quest Fluo-8 NW钙测定试剂盒提供均匀的荧光测定，用于检测细胞内钙动员。表达感兴趣的GPCR的细胞通过钙预先加载我们专有的Fluo-8 NW，其可以穿过细胞膜。 Fluo-8 NW是可用于HTS筛选的最亮钙指示剂。一旦进入细胞内，Fluo-8 NW的亲脂性阻断基团被非特异性细胞酯酶切割，产生带负电荷的荧光染料，其停留在细胞内，并且在与钙结合时其荧光大大增强。当用筛选化合物刺激细胞时，该受体表明细胞内钙的释放，这极大地增加了Fluo-8 NW的荧光。其长波长，高灵敏度和100-250倍荧光增加的特性（当它与钙形成复合物时）使Fluo-8 NW成为测量细胞钙的理想指标。这个Screen Quest Fluo-8 NW钙测定试剂盒提供了一种优化的检测方法，用于监测G蛋白偶联受体（GPCR）和钙通道。该测定可以以方便的96孔或384孔微量滴定板形式进行，并且易于适应自动化。金畔生物是AAT Bioquest的中国代理商，为您提供最优质的Screen Quest Fluo-8 去除培养基钙检测试剂盒*适合于难检测细胞系*。 

点击查看光谱

样品实验方案

简要概述

1.准备细胞
2.去除生长培养基
3.添加Fluo-8 NW染料工作溶液
4.在室温下孵育1小时
5.监测Ex / Em = 490 / 525nm处的荧光强度

溶液配制

1.储存溶液配制

除非另有说明，否则所有未使用的储备溶液应分成一次性等分试样，并在制备后储存在-20°C。 避免反复冻融循环。
1.1 Fluo-8 NW配制：
对于Cat No.36307，将10μLDMSO加入Fluo-8 NW（组分A）中，并充分混合。
对于Cat No.36308和36309，将100μLDMSO加入Fluo-8 NW（组分A）中，并充分混合。 注意：10μLFluo-8 NW原液足以容纳1个平板。

1.2分析缓冲液储备液（1X）：
对于Cat No.36307和36308，将9mL HHBS（组分C）加入10X Pluronic F127 Plus（1mL，组分B）中并充分混合。
对于Cat No.36309，将整瓶10XPluronic®F127Plus（10 mL，组分B）加入90 mL HHBS缓冲液（不包括在试剂盒中）中并充分混合。 注意：对于一个平板，10 mL的1X分析缓冲液就足够了。

2.工作溶液配制

将10μLFluo-8 NW DMSO储备溶液加入10mL 1X测定缓冲液中并充分混合。 该工作溶液在室温下稳定至少2小时。

操作步骤

1.有关细胞样品制备的指南，请点击查看。

2.从细胞板上除去生长培养基。注意：重要的是去除生长培养基，以最大限度地减少背景荧光和化合物对血清或培养基的干扰。注意：或者，在含有0.5％至1％FBS的生长培养基中培养细胞，以避免培养基去除步骤。在这种情况下，需要在HHBS缓冲液中加入2X染料。 [我们为那些在生长培养基中使用0.5％至1％FBS以避免培养基去除步骤的人提供2个独立的无洗涤钙测定试剂盒（目录号36315和目录号36316）。

3.将100μL/孔（96孔板）或25μL/孔（384孔板）的Fluo-8NW染料工作溶液加入到细胞板中。

4.将染料加载板在细胞培养箱中孵育30分钟，然后在室温下将板孵育另外30分钟。注意：如果测定需要37°C，立即进行实验，无需进一步室温孵育。注意：如果细胞在室温下运行时间较长，可在室温下孵育细胞培养板1-2小时（建议培养时间不超过2小时。）

5.用HHBS或所需缓冲液制备复合板。

6.通过监测Ex / Em = 490 / 525nm处的荧光强度来进行钙通量测定。注意：在实验之前运行信号测试很重要。不同的仪器有自己的强度范围。将信号测试强度调整到最大强度计数的10％至15％的水平。例如，FLIPR-384的最大荧光强度计数为65,000，因此应调整仪器设置以使其信号测试强度在7,000到10,000左右。

数据分析

        从空白标准孔获得的读数（RFU（Max-Min））用作阴性对照。 从其他标准的读数中减去该值，以获得基线校正值。 然后，绘制标准读数以获得标准曲线和方程。 该等式可用于计算卡巴胆碱剂量样品。 

参考文献

2-OMe-lysophosphatidylcholine analogues are GPR119 ligands and activate insulin secretion from βTC-3 pancreatic cells: Evaluation of structure-dependent biological activity
Authors: Anna Drzazga, Agata Sowińska, Agnieszka Krzemińska, Andrzej Okruszek, Piotr Paneth, Maria Koziolkiewicz, Edyta Gendaszewska-Darmach
Journal: Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids (2017)

A new electro-optical approach for conductance measurement: an assay for the study of drugs acting on ligand-gated ion channels
Authors: A Menegon, S Pitassi, N Mazzocchi, L Redaelli, R Rizzetto, JF Rolland, C Poli, M Imberti, A Lanati, F Grohovaz
Journal: Scientific Reports (2017)

Altered spontaneous calcium signaling of in situ chondrocytes in human osteoarthritic cartilage
Authors: Xiaoyuan Gong, Wenbin Xie, Bin Wang, Lingchuan Gu, Fuyou Wang, Xiang Ren, Cheng Chen, Liu Yang
Journal: Scientific reports (2017): 17093

Analysis of Ca2+ response of osteocyte network by three-dimensional time-lapse imaging in living bone
Authors: Tomoyo Tanaka, Mitsuhiro Hoshijima, Junko Sunaga, Takashi Nishida, Mana Hashimoto, Naoya Odagaki, Ryuta Osumi, Taiji Aadachi, Hiroshi Kamioka
Journal: Journal of Bone and Mineral Metabolism (2017): 1–10

Aryl-and alkyl-phosphorus-containing flame retardants induced mitochondrial impairment and cell death in Chinese hamster ovary (CHO-k1) cells
Authors: Chao Huang, Na Li, Shengwu Yuan, Xiaoya Ji, Mei Ma, Kaifeng Rao, Zijian Wang
Journal: Environmental Pollution (2017): 775–786

Bystander effects elicited by single-cell photo-oxidative blue-light stimulation in retinal pigment epithelium cell networks
Authors: Masaaki Ishii, Bärbel Rohrer
Journal: Cell Death Discovery (2017): 16071

Ca 2+ signals initiate at immobile IP 3 receptors adjacent to ER-plasma membrane junctions
Authors: Nagendra Babu Thillaiappan, Alap P Chavda, Stephen C Tovey, David L Prole, Colin W Taylor
Journal: Nature Communications (2017): 1505

Cells smell on a CMOS: A portable odorant detection system using cell-laden collagen pillars
Authors: Yusuke Hirata, Yuya Morimoto, Eunryel Nam, Shotaro Yoshida, Shoji Takeuchi
Journal: (2017): 13–16

Ex vivo replication of phenotypic functions of osteocytes through biomimetic 3D bone tissue construction
Authors: Qiaoling Sun, Saba Choudhary, Ciaran Mannion, Yair Kissin, Jenny Zilberberg, Woo Y Lee
Journal: Bone (2017)

High Glucose Enhances Isoflurane-Induced Neurotoxicity by Regulating TRPC-Dependent Calcium Influx
Authors: ZhongJie Liu, ChangQing Ma, Wei Zhao, QingGuo Zhang, Rui Xu, HongFei Zhang, HongYi Lei, ShiYuan Xu
Journal: Neurochemical Research (2017): 1–14

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