Cell Death / Health Assays Products & Reviews

ProQinase's CL100-ProliFiler is a standard service package comprising IC50 determination of your test compounds on the proliferation response of a defined panel of 100 tumor cell lines.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

10 x 1.5 ml, sufficient for 1,500 counts (10 µl/count), 0.4% in 0.81% sodium chloride and 0.06% potassium phosphate dibasic solution, sterile filtered, for use with TC10™ or TC20™ automated cell counter.

Use the CFDA-SE (5[6]Carboxyfluorescein diacetate, succinimidyl ester) cell-permeable dye to monitor cell population health.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

VivaFix™ Cell Viability Assays enable researchers to accurately discriminate between live and dead cells in fixed or unfixed samples by cell staining prior to flow cytometry, cell sorting and microscopy.

Commonly used in flow cytometry experiments for excluding dead cells, the propidium iodide solution enters a compromised cell and binds to double-stranded DNA/RNA by intercalating between base pairs.

The ReadiDrop™ 7-aminoactinomycin D (7-AAD) cell viability assay is designed as a ready-to-use 7-AAD solution, which binds double-stranded DNA with a high-affinity intercalation between GC base pairs.

CytoTrack cell proliferation assays are designed to efficiently stain live cells for excellent resolution of each cell division generation.

CytoTrack cell proliferation assays are designed to efficiently stain live cells for excellent resolution of each cell division generation.

CytoTrack cell proliferation assays are designed to efficiently stain live cells for excellent resolution of each cell division generation.

1 x 96-well, includes magnetic capture beads, detection antibodies, standards, controls, diluent, buffers, streptavidin-PE, flat bottom plate, and plate seals, for the detection of 6 human kidney toxicity markers in urine

1 x 96-well, includes magnetic capture beads, detection antibodies, standards, controls, diluent, buffers, streptavidin-PE, flat bottom plate, and plate seals, for the detection of 6 human kidney toxicity markers in urine

0.4%, liquid, sterile-filtered, suitable for cell culture  

≥98% (HPLC)  

LDH-Glo™ Cytotoxicity Assay detects cell death from a small number of cells, including 3D cell cultures, based on the release of lactate dehydrogenase.

The RealTime-Glo™ Annexin V Apoptosis and Necrosis Assay provides a no-wash, one-step Annexin V assay that allows continual monitoring of cell state to determine apoptotic onset using a plate-reading luminometer.

The Caspase-Glo ® 1 Inflammasome Assay  directly measures inflammasome activation with a simple add-mix-measure protocol.

Antibody-dependent cell-mediated cytotoxicity (ADCC) is a mechanism of action of antibodies through which virus-infected or other diseased cells are targeted for destruntion by components of the cell-mediated.

Cell Counter & Spectrometer in the palm of your hand.

Combining the sensitivity of a fluorescence-based assay with a microplate format enables a rapid, quantitative readout suitable for high-throughput analysis. In a microplate well, the fluorescent signal can be generated within whole cells, in cell lysates, or in purified enzyme preparations and may then be analyzed by measuring fluorescence intensity from the well without the need for cellular imaging.