keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
1) Non-toxicity: The unique oiliness and high molecular weight characteristics of CelRed prevent it from penetrating cell membranes into cells, and Ames test results also show that the mutagenicity of CelRed dye is much less than EB. 2) High sensitivity: suitable for electrophoretic staining of various fragments of different sizes, with less influence on nucleic acid migration than SYBR Green I. 3) High stability: suitable for preparation of agarose gel by microwave or other heating methods;Extremely stable in acid or alkali buffer at room temperature and light resistant. 4) High SIGNal-to-noise ratio: the sample fluorescence signal is strong, while the background signal is low. 5) Simple operation: like EB, the dye does not degrade in the prefabricated gel and electrophoresis process;The dyeing process after electrophoresis takes only 30 minutes without decolorization or washing, and can be directly observed by ultraviolet gel transmission instrument. 6) Wide range of application: pre-electrophoresis staining (gel dyeing) or post-electrophoresis staining (bubble dyeing) is optional;Suitable for agarose gel or polyacrylamide gel electrophoresis;Can be used for dsDNA, ssDNA or RNA staining.
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
100 μL | ¥ 387 | 待询 |
产品描述 | 1) Non-toxicity: The unique oiliness and high molecular weight characteristics of CelRed prevent it from penetrating cell membranes into cells, and Ames test results also show that the mutagenicity of CelRed dye is much less than EB. 2) High sensitivity: suitable for electrophoretic staining of various fragments of different sizes, with less influence on nucleic acid migration than SYBR Green I. 3) High stability: suitable for preparation of agarose gel by microwave or other heating methods;Extremely stable in acid or alkali buffer at room temperature and light resistant. 4) High SIGNal-to-noise ratio: the sample fluorescence signal is strong, while the background signal is low. 5) Simple operation: like EB, the dye does not degrade in the prefabricated gel and electrophoresis process;The dyeing process after electrophoresis takes only 30 minutes without decolorization or washing, and can be directly observed by ultraviolet gel transmission instrument. 6) Wide range of application: pre-electrophoresis staining (gel dyeing) or post-electrophoresis staining (bubble dyeing) is optional;Suitable for agarose gel or polyacrylamide gel electrophoresis;Can be used for dsDNA, ssDNA or RNA staining. |
体外活性 |
GelRed for Electrophoresis In Gel Staining (Pre-staining, same method as EB) Prepare a agarose solution and heat till it dissolves. GelRed Nucleic Acid Staining solution is diluted from the GelRed Nucleic Acid Stain 1:10,000 prior to pouring the gel. Since good thermal stability, GelRed can be added directly to hot agarose solution. Shake to ensure being fully mixed flowing by cast the gel, Run gel and view results by UV projector. |
分子量 | N/A |
CAS No. | TD0002 |
keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
CelRed nucleic acid gel stain *10,000× concentrate in water* TD0002 Inhibitor inhibitor inhibit