Our product Cell Counting Package deal-8 (CCK-8) current a further useful and delicate approach for the evaluation of cell amount dedication and cell proliferationtotoxicity assay than earlier strategies. The tools makes use of a extraordinarily water-soluble tetrazolium salt, WST-8, which produces a water-soluble formazan dye upon low cost inside the presence of an electron mediator. The amount of the formazan generated by dehydrogenases is straight in proportion to the numbers of residing cells. The detection sensitivity by CCK-Eight is bigger than completely different tetrazolium salts resembling MTT, XTT, MTS or WST-1.
Background
Cell proliferation shall be detected by numerous methods. Cell proliferation induces an increase inside the train of the mitochondrial dehydrogenases, which cleaves the tetrazolium salt to formazan.
The WST Cell Proliferation Colorimetric Assay Package deal plus provides the most effective and most delicate technique for quantification of cell proliferation and viability. Cell proliferation causes the rise inside the amount of formazan dye long-established that is straight proportional to the number of residing cells and shall be quantified by measuring the absorbance of the dye decision at 440 nm using microtiter plate reader. The tools might be utilized for the analysis of cell proliferation in response to pharmaceutical compounds, cytotoxic compounds like anticancer drugs and plenty of completely different toxic brokers.
The assay may additionally be used for the detection of cell proliferation in response to cytokines, mitogens, progress components and nutritional vitamins, and so forth. The assay might be very easy and straightforward, merely add-and-read, requiring no solubilization, no washing and no harvesting steps, and is regular, sooner and further delicate than MTS, MTT or XTT-based assays. Your total assay shall be carried out in a microtiter plate and correlates properly with the [3H]-thymidine incorporation assay.
| Choices | Fast and useful Simple one-step course of; takes decrease than 4 hours. Makes use of a water-soluble tetrazolium salt WST reagent. The technique is very easy that requires no washing/harvesting/or solubilization steps and is faster and further delicate than MTT/XTT/or MTS-based assays. Your total assay shall be carried out straight in a 96-well plate. |
| Supply | Gel pack |
| Storage Circumstances | Retailer at -20°C. |
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- 2. Xiangli Zhuang, Bo Wu, et al. “Influence of Xingbi Gel Nasal Drops on Fyn-STAT5 Pathway in Nasal Mucosa Fibroblasts of Guinea Pigs with Allergic Rhinitis.” Evid Based Complement Alternat Med. 2021 Mar 20;2021:6686815. PMID:33824677
- 3. Rui-Qi Wang, Xiao-Ran Prolonged, et al. “Lnc-GAN1 expression is said to good survival and suppresses tumor growth by sponging mir-26a-5p to activate PTEN signaling in non-small cell lung most cancers.” J Exp Clin Most cancers Res. 2021 Jan 6;40(1):9. PMID:33407724
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) Cell Counting Kit-8 (CCK-8) |
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| K1018-10 | ApexBio | 2x5 ml (1000 tests) | EUR 166 |
Cell Counting Kit-8 (CCK-8) |
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| K1018-100 | ApexBio | 20x5 ml (10000 tests) | EUR 885 |
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| K1018-30 | ApexBio | 6x5 ml (3000 tests) | EUR 328 |
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| K1018-5 | ApexBio | 1x5 ml (500 tests) | EUR 119 |
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| B34302 | Bimake | 5 mL (500 ractions) | EUR 130 |
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Description: The Bimake Cell Counting Kit-8 (CCK-8) is a fluorescent assay for the determination of cell viability in vitro. Results are obtained in only 3 steps: addition, incubation and reading. |
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Cell Counting Kit-8 (CCK-8) |
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| B34304 | Bimake | 25 mL (2500 ractions) | EUR 315 |
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Description: The Bimake Cell Counting Kit-8 (CCK-8) is a fluorescent assay for the determination of cell viability in vitro. Results are obtained in only 3 steps: addition, incubation and reading. |
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Description: The CytoSelect BrdU Cell Proliferation ELISA Kit detects BrdU incorporated into cellular DNA during cell proliferation using an anti-BrdU antibody. When cells are incubated in media containing BrdU, the pyrimidine analog is incorporated in place of thymidine into the newly synthesized DNA of proliferating cells. Once the labeling media is removed, the cells are fixed and the DNA is denatured in one step with a fix/denature solution (denaturation of the DNA is necessary to improve the accessibility of the incorporated BrdU for detection). Then an anti-BrdU mouse monoclonal antibody is added followed by an HRP conjugated secondary antibody to detect the incorporated BrdU. The magnitude of the absorbance for the developed color is proportional to the quantity of BrdU incorporated into cells and can be directly correlated to cell proliferation. |
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