ATP-Red 1; 纯度: ge;98.0%
ATP-Red 1 是一种多位点结合可切换的荧光探针,能够选择性的快速检测活细胞中的 ATP 含量。

ATP-Red 1 Chemical Structure
CAS No. : 1847485-97-5
规格 | 价格 | 是否有货 | 数量 |
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1 mg | ¥3900 | In-stock | |
5 mg | ¥8600 | In-stock | |
10 mg | ¥14000 | In-stock | |
25 mg | ¥24000 | In-stock | |
50 mg | ; | 询价 | ; |
100 mg | ; | 询价 | ; |
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ATP-Red 1 相关产品
bull;相关化合物库:
- Bioactive Compound Library Plus
生物活性 |
ATP-Red 1 is a multisite-binding switchable fluorescent probe, and can selectively and rapidly responds to intracellular concentrations of ATP in living cells. |
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体外研究 (In Vitro) |
ATP-Red 1 is a multisite-binding switchable fluorescent probe, and can selectively and rapidly responds to intracellular concentrations of ATP in living cells. The maximum absorption and emission wavelength of are 570/566 nm and 590/585 nm. ATP-Red 1 has good membrane permeability, and in the presence of 5 mM ATP, the fluorescence intensity of ATP-Red 1 increases 5.6-fold. ATP-Red 1 (2.5 μM, 20 min) shows much weaker fluorescence after KCN-induced inhibition of OXPHOS, which results in reduced mitochondrial ATP levels in OSCC cells[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
561.48 |
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Formula |
C34H36BN3O4 |
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CAS 号 |
1847485-97-5 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4deg;C, protect from light *In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:;
DMSO : 50 mg/mL (89.05 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 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,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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Cell Assay [1] |
OSCC Cells are plated in 96-well flat-bottomed plates at 1×105 cells per well and allowed to grow 3 or 24 h prior to exposure to ATP-Red 1. Then MTT reagent is added for 4 h at 37 °C and DMSO (100 μL/well) is further incubated with cells for 15 min after removing the medium. The absorbance at 570 nm and 690 nm (background signal) is recorded in a Spectra Max M2 microplate reader. The following formula is used to calculate the viability of cell growth: Cell viability (%) = (mean of A value of treatment group / mean of A value of control) × 100[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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参考文献 |
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