Provides a comprehensive research system for the reliable, in-depth characterization of differentiation stages of human neural stem cells (hNSCs) from a heterogeneous culture

BD Horizon™ Brilliant Stain Buffer is a buffer for the immunofluorescent staining of cells.

Measure nitric oxide (NO) composition and total as separate values of nitrate (NO3-) and nitrite (NO2-) levels in serum, plasma, urine, saliva and other biological fluids.

Serves as a sensitive probe for flow cytometric analysis of cells that are undergoing apoptosis

Useful with a variety of fluorescence-detection methodologies

Optimized reagent for analysis of apoptotic cells

Staining precedes the loss of membrane integrity which accompanies the latest stages of cell death resulting from either apoptotic or necrotic processes

Optimized for fluorescence microscopy applications

The most sensitive, fastest, homogeneous cell viability assay. Based on luminescent detection of ATP.

Caspase-Glo™ 3/7 Assay is a homogeneous luminescent assay that measures caspase-3/7 activities

Used for quantitative measurement of total nitric oxide.

Measures nitrite (NO₂^-), one of two primary stable and nonvolatile breakdown products of nitric oxide (NO)

The CellTiter-Glo™ 2.0 Assay provides a homogeneous method of determining the number of viable cells in culture by quantitating the amount of ATP present, which indicates the presence of metabolically active cells.

Serves as a sensitive probe for flow cytometric analysis of cells that are undergoing apoptosis

Fluorescent labeling of proliferating cells is accurate and compatible with antibody methods due to the mild click protocol

One assay for all your kinase screening needs. The assay is well suited for measuring the effects of chemical compounds on the activity of many purified kinases, making it ideal for primary screening as well as kinase selectivity profiling.

Contains apoptotic program characterized by certain morphologic features, including loss of plasma membrane asymmetry and attachment, condensation of the cytoplasm and nucleus, and internucleosomal cleavage of DNA

Homogeneous, colorimetric cell viability assay. Requires a 1- to 4-hour incubation.

Detects and quantifies apoptotic cells within a cell population

The HDAC-Glo Class IIa and HDAC-Glo 2 Assays are single-reagent-addition homogeneous, luminescent assays that measure the relative activity of histone deacetylase (HDAC) Class IIa and Class I enzyme 2 from cells, extracts or purified enzyme sources.

Single-reagent-addition,homogeneous, luminescent assays that measure the relative activity of the NAD+-dependent histone deacetylase (HDAC) class III enzymes (sirtuins; SIRTs) from purified enzyme sources

Has high affinity for PS, and binds to cells with exposed PS

AlamarBlue™ Cell Viability Reagent

The ApoLive-Glo™ Multiplex Assay measures both the number of viable cells as a marker of cytotoxicity and caspase activation as a marker of apoptosis within a single assay well to determine the mechanism of cell death.

The ONE-Glo™ + Tox Assay combines luciferase assay chemistry with a cell viability marker to better understand reporter gene expression in the context of cell health. The assay uses a two-step, addition-only process to measure in a single well of a plate.

Compatible with intracellular staining. Pre-titrated and tested on mouse thymocytes cultured overnight in medium (to induce apoptosis) or on Jurkat cells treated with 10 μM Camptothecin for 4 hours. Both the Annexin V APC and the Propidium iodide components can be used at 5μL per test

Staining precedes the loss of membrane integrity which accompanies the latest stages of cell death resulting from either apoptotic or necrotic processes.

For measuring effects chemical compounds have on activity of broad range of purified kinases, making it ideal for both primary screening as well as kinase selectivity profiling

Colorimetric method for estimating the number of nonviable cells present in a sample