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QIA127 Rapid Cell Proliferation Kit

Rapid Cell Proliferation Kit: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。
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QIA127
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概要

Replacement Information

主要スペック表

Detection Methods
Colorimetric

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      Description
      OverviewAssay measures the increased activity of cellular mitochondrial dehydrogenases that can cleave the tetrazolium dye WST-1 to formazan. The formazan formation is then quantified by measuring the change in absorbance at 450 nm in a microplate reader. The activity of mitochondrial dehydrogenases is proportional to cell number. No washing, harvesting, or solubilization steps are required.
      Catalogue NumberQIA127
      Brand Family Calbiochem®
      Materials Required but Not Delivered• Pipettors with disposable tips
      • Tissue culture grade, flat-bottom 96-well plate
      • Spectrophotometer capable of measuring absorbance in 96-well plates at a wavelength of 440-460 nm
      References
      ReferencesIshiyama, M., et al. 1995. In Vitro Toxicology 8, 187.
      Liu, S.O., et al 1995. Nat. Med. 1, 267.
      Ishiyama, M., et al. 1993. Chem. Pharm. Bull. 41, 1118.
      Product Information
      Detection methodColorimetric
      Form500 Tests
      Format96-well plate
      Kit containsWST-1, 1-Methoxy PMS, and a user protocol.
      Quality LevelMQ100
      Applications
      Biological Information
      Assay range1000 - 50,000 Cells
      Assay time0.5 - 4 h
      Sample TypeCultured cells
      Physicochemical Information
      Sensitivity1000 cells (adherent); 2500 cells (nonadherent)
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Intended useThe Calbiochem® Rapid Cell Proliferation Kit is designed to determine the number of viable cells in proliferation, or cytotoxicity studies, based on the cleavage of the tetrazolium salt WST-1 by mitochondrial dehydrogenases in viable cells. The assay can be used to measure cell proliferation in response to growth factors or cytokines, or to assess cytotoxic compounds.
      Storage and Shipping Information
      Ship Code Dry Ice Only
      Toxicity Multiple Toxicity Values, refer to MSDS
      Storage -20°C
      Storage ConditionsUpon arrival store the entire contents of the kit at -20°C.
      Protect from Light Protect from light
      Avoid freeze/thaw Avoid freeze/thaw
      Do not freeze Ok to freeze
      Packaging Information
      Transport Information
      Supplemental Information
      Kit containsWST-1, 1-Methoxy PMS, and a user protocol.
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      QIA127-1KITCN 07790788054021

      Documentation

      Rapid Cell Proliferation Kit (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      Rapid Cell Proliferation Kit 試験成績書（CoA）

      タイトルロット番号
      QIA127

      参考資料

      参考資料の概要
      Ishiyama, M., et al. 1995. In Vitro Toxicology 8, 187.
      Liu, S.O., et al 1995. Nat. Med. 1, 267.
      Ishiyama, M., et al. 1993. Chem. Pharm. Bull. 41, 1118.
      ユーザープロトコール

      Revision11-September-2008 RJH
      Form500 Tests
      Format96-well plate
      Detection methodColorimetric
      StorageUpon arrival store the entire contents of the kit at -20°C.
      Intended useThe Calbiochem® Rapid Cell Proliferation Kit is designed to determine the number of viable cells in proliferation, or cytotoxicity studies, based on the cleavage of the tetrazolium salt WST-1 by mitochondrial dehydrogenases in viable cells. The assay can be used to measure cell proliferation in response to growth factors or cytokines, or to assess cytotoxic compounds.
      BackgroundCell proliferation assays are widely used in cell biology to study growth factors, cytokines, and media components, to screen cytotoxic agents, and for lymphocyte activation. The use of tetrazolium salts such as MTT commenced in the 1950s, and is based on the fact that live cells reduce tetrazolium salts into colored formazan compounds. The biochemical procedure is based on the activity of mitochondrial enzymes, which are inactivated shortly after cell death. The new cell proliferation reagent WST-1 has several advantages as compared to MTT. WST-1 yields water-soluble cleavage products like XTT, which can be measured without an additional solubilization step, and WST-1 has a wider range than MTT or XTT.
      Principles of the assayThe Calbiochem® Rapid Cell Proliferation Kit provides a colorimetric assay for the fast and convenient determination of viable cell numbers in cell proliferation and cell cytotoxicity assays. After mixing the two components supplied in the kit the mixed solution is added to the wells of a 96-well plate (tissue culture plate) that contains cultivated cells. The intensity of the dye is proportional to the number of viable cells and the absorbance is read with a microplate reader at 440-460 nm after a 0.5-4 h incubation at 37°C.
      Materials provided• WST-1 Reagent (Kit Component No. JA7700-1EA): 1 vial, supplied as a powder in an amber glass bottle
      • Electron Mediator Solution (EMS) (Kit Component No. JA7701-5ML): 1 vial, 5 ml in an amber glass bottle
      Materials Required but not provided• Pipettors with disposable tips
      • Tissue culture grade, flat-bottom 96-well plate
      • Spectrophotometer capable of measuring absorbance in 96-well plates at a wavelength of 440-460 nm
      Reagent preparation• WST-1 Labeling Mixture: Thaw the EMS solution at room temperature or in a 37°C water bath. Add the entire contents of this solution to the bottle containing the WST-1 reagent. The mixed solution can be stored at 4°C for several weeks. For long-term storage (several months) aliquot and store at -20°C. Protect from light.
      Detailed protocol1. Grow cells in a tissue culture grade, flat-bottom plate in 100 µl of culture medium per well in a CO2 tissue culture incubator. For cell stimulation assays a starting concentration of 5,000-25,000 cells per well is recommended, for cytotoxicity assays the recommended number of cells per well is 25,000-150,000.
      2. After incubation add 10 µl of the WST-1 labeling mixture, prepared as above, to each well. Mix briefly by shaking gently for several min.
      3. Incubate adherent cells for 1-2 h and suspension cells for 3-4 h.
      4. Measure the absorbance of the samples using a microplate reader at a wavelength of 440-460 nm. If a reference wavelength is to be subtracted, a filter above 600 nm is recommended. The background absorbance is dependent upon the culture medium, pH, incubation time, and time of exposure to light. The typical background absorbance after a 2 h incubation is 0.1-0.2 absorbance units.
      Example data

      Figure 1: Example

      NIH3T3 cells incubated with WST-1 labeling mixture for 2.5 h at 37°C as described above.

      Figure 2: No. NIH3T3 Cells vs. Abs 450 nm

      NIH3T3 cells incubated with WST-1 labeling mixture for 2.5 h at 37°C as described previously.

      Figure 3: No. HT-1080 Cells vs. Abs 450 nm

      HT-1080 cells incubated for 20 h followed by the addition of WST-1 labeling mixture. After additional 1 (Δ), 2.5 (⊄), and 4 h (•) incubations the absorbance was read at 450 nm.

      Figure 4: Inductions of Apoptosis in Jurkat Cells

      100,000 Jurkat cells per well were incubated overnight at 37°C in the presence of 0, 1, or 5 µg/ml camptothecin in RPMI medium containing 2% FBS. After the incubation 10 µl of the WST-1 labeling mixture was added and absorbance was read after a 2.5 h incubation at 37°C.
      Sensitivity1000 cells (adherent); 2500 cells (nonadherent)
      Assay Range1000 - 50,000 Cells
      Registered TrademarksCalbiochem® is a registered trademark of EMD Chemicals, Inc.
      Interactive Pathways™ is a trademark of EMD Chemicals, Inc.