Cell Culture Contamination Detection Kit

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Get tips on using DMEM/Ham's F-12 liquid medium w/o L-Glutamine to perform Stem cell culture media Human Tendon Stem/Pluripotence cells (TSPCs)

Products Bio Sell DMEM/Ham's F-12 liquid medium w/o L-Glutamine

Get tips on using Corning® 500 mL MEM (Minimum Essential Medium) Alpha Medium to perform Stem cell culture media Cord blood-derived endothelial cells(hCBiPS2)

Products Corning Corning® 500 mL MEM (Minimum Essential Medium) Alpha Medium

Get tips on using Gibco™ DMEM/F-12, GlutaMAX™ supplement to perform Stem cell culture media Choroid plexus-like tissue generation from SFEBq

Products Thermo Fisher Scientific Gibco™ DMEM/F-12, GlutaMAX™ supplement

Cell cytotoxicity assays measure the ability of certain compounds or chemical mediators to reduce the viability of the cells. The term cell cytotoxicity assay can sometimes be used interchangeably with cell proliferation assay. Healthy living cells can be identified by the use of formazan dyes, protease biomarkers or by measuring ATP content. The formazan dyes are chromogenic products formed by the reduction of tetrazolium salts by dehydrogenases, such as lactate dehydrogenase (LDH) and reductases that are released during cell death. Common tetrazolium salts include INT, MTT, MTS and XTT. Cell cytotoxicity can also be measured by using the SRB and WST-1 assays. These assays can usually be used in a high-throughput fashion and can be quantitated by measuring absorbance, colorimetry or luminescence. All these assays require similar numbers of cell plating at the initiation, a time course of treatment with the cytotoxic agent and at least triplicates for each condition at every point of analysis. Cell shrinkage, plasma membrane blebbing, cell detachment, externalization of phosphatidylserine, nuclear condensation and ultimately DNA fragmentation are well-described features of apoptosis. The assays that rely on cell membrane integrity for their function, may not be able to quantify early apoptosis. Therefore, in order to distinguish early apoptotic vs. late apoptotic or necrotic cells, additional flow cytometry techniques can be used. A combination of Annexin V and PI (propidium iodide) can be used to distinguish early (Annexin V+/PI-) and late apoptotic (Annexin V+/PI+) cells. Sometimes, caspase assays are used in order to differentiate the stages of apoptosis.

Cellular assays Cell cytotoxicity / Proliferation assay cell type adipose stem cells

Get tips on using Autophagy Assay Kit to perform Autophagy assay cell type - Beas-2B

Products Sigma-Aldrich Autophagy Assay Kit

Get tips on using Autophagy Assay Kit to perform Autophagy assay cell type - Mouse cardiomyocytes

Products Sigma-Aldrich Autophagy Assay Kit

Get tips on using Corning® 1L DMEM (Dulbecco’s Modified Eagle’s Medium)/F12 50:50 Mix to perform 3D Cell Culture Media Mouse fallopian organoids

Products Corning Corning® 1L DMEM (Dulbecco’s Modified Eagle’s Medium)/F12 50:50 Mix

Get tips on using AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit to perform Cell line authentication Endometrial Adenocarcinoma cell line HEC-1B

Products Thermo Fisher Scientific AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit

Get tips on using AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit to perform Cell line authentication Ovarian cancer cell line PA-1

Products Thermo Fisher Scientific AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit

Get tips on using AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit to perform Cell line authentication Renal carcinoma cell line Caki-1

Products Thermo Fisher Scientific AmpFLSTR™ Identifiler™ Plus PCR Amplification Kit

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