Cell Proliferation/Viability Assays

Genotype: F - ompT hsdS B (r B - m B - ) gal dcm (DE3) This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their

The Live-Dead Cell Viability Assay Kit is a quick and simple three-color assay to measure cell viability. The kit consists of Calcein-AM (stains live cells), Propidium Iodide (stains dead cells) and Hoechst 33342 (stains all cells).

MTT is a pale yellow substrate that is cleaved by living cells to yield a dark blue formazan product. This process requires active mitochondria, and even freshly dead cells do not cleave significant amounts of MTT.

MTT is a pale yellow substrate that is cleaved by living cells to yield a dark blue formazan product. This process requires active mitochondria, and even freshly dead cells do not cleave significant amounts of MTT.

PrEST Antigen SIPA1L3 signal induced proliferation associate

PrEST Antigen SIPA1L3 signal-induced proliferation-associate

Genotype: F &#8211 ompT hsdS B (r B &#8211 m B &#8211 ) gal dcm lacY1 ahpC (DE3) gor522 ::Tn 10 trxB pLacIRARE (Cam R , Kan R , Tet R ) This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives

This DMEM F-12 Ham medium differs from the original formula, because it is supplemented with L-alanyl-L-glutamine dipeptide. Glutamine is notoriously unstable in cell culture.

ViaFluor&reg SE Cell Proliferation Kits use amine-reactive dyes to covalently label the cell cytoplasm, and are used to monitor cell division by flow cytometry. The dyes also can be used to stably label cells to image cell morphology, or to track

Of borosilicate glass, with Clear-Seal Standard Taper 19/22 joints Meets demands of basic organic chemistry procedures Kit range can be expanded as needed by adding other standard glassware Usable interchangeably with Standard Taper ground joints,

XTT Cell Viability Assay Kit provides a simple method for determining live cell numbers using standard photometric microplate readers. Determination of live cell numbers is often used to assess the rate of cell proliferation and to screen cytotoxic