Cell Function Reagents and Kits
Cell Function Reagents and Kits
BD Horizon™ Brilliant Stain Buffer is a buffer for the immunofluorescent staining of cells.
Used to stain nucleic acids in live or fixed cells. BD Pharmingen™ DRAQ5™ is also used for cell cycle analysis by DNA content, nuclear visualization, or discrimination of nucleated cells from debris or enucleated cells.
|Reactivity||Tested in Development: Human, Mouse; Reported Reactivity: Rat|
|For Use With (Application)||Bioimaging,Immunofluorescence,Intracellular Staining (Flow Cytometry)|
|Dye Type||DNA dye|
|Excitation Wavelength Range||598/646 nm|
Live cancer stem cell assay using green-shifted fluorescent dye for ALDH
Purified from pooled rat plasma.
Designed with the inclusion of fluorescent antibodies specific for incorporated BrdU, phosphorylated H2AX (γH2AX) and cleaved PARP
Kit contains a combination of mouse monoclonal antibody conjugates
Ready-to-use solution of the nucleic acid dye, 7-Amino-actinomycin D (7-AAD) that can be used in place of propidium iodide (PI) for the exclusion of nonviable cells in flow cytometric assays
|Content And Storage||4°C|
Stain live or fixed cells with this far-red DNA stain.
Extract protein from yeast two-hybrid reporter systems and measure beta-galactosidase activity using compatible Y-PER Reagent and b-Gal Assay Reagent.
Lyse cultured mammalian cells and measure beta-galactosidase activity using compatible M-PER Cell Lysis Reagent and colorimetric b-Gal Assay Reagent.
For colorimetric quantitation of viable cell number in proliferation and cytotoxicity assays.
|Content And Storage||Stored at -20°C for long-term|
|For Use With (Application)||Research|
Designed for mitophagy detection in mammalian cells.
Detect senescent cells with much higher sensitivity than X-gal.
For the robust feeder-free expansion of human NK cells ex vivo.
For the differentiation of Th1 cells from a preparation of CD4+ T cells isolated from mouse splenocytes.
For the expansion of human CD3+CD56+ Cytokine-induced Killer (CIK) cells from peripheral blood mononuclear cells (PBMCs).
For the differentiation of Th2 cells from a preparation of CD4+ T cells isolated from mouse splenocytes.
For the proliferative expansion of human B cell populations.
For the expansion of human CD3-CD56+ NK Cells from peripheral blood mononuclear cells (PBMCs).
Homogeneous, colorimetric cell viability assay; requires mixing of MTS and PMS components prior to assay, then a 1- to 4-hour incubation. Standalone MTS powder for applications where optimization of assay for specific cell types or conditions is desired.
|Content And Storage||-30°C to -10°C|
|For Use With (Application)||Determining the number of viable cells in proliferation,Cytotoxicity or Chemosensitivity Assays,Cell Viability,Chemotaxis|
Luminescent assay measures number of viable cells in culture.
The Viral ToxGlo™ Assay is a simple, quantifiable method of determining viral-induced cytopathic effects (CPE) in host cells caused by lytic virions. The assay measures cellular ATP as a surrogate measure of host cell viability.
|Content And Storage||-30°C to -10°C.|
|For Use With (Application)||Determining viral-induced cytopathic effects (CPE) in host cells caused by lytic virions|
The MultiTox-Fluor Multiplex Cytotoxicity Assay is a single-reagent-addition, homogeneous, fluorescent assay that measures the number of live and dead cells simultaneously in culture wells.