Cell-Based Assays Products & Reviews

The Quick Western Kit provides a universal detection reagent that can be combined with the primary antibody incubation step, eliminating the need for a secondary antibody incubation step.

IRDye 680RD is the near-infrared fluorescent dye of choice for applications in the 700 nm wavelength, especially Western blots, cell-based assays such as the In-Cell Western assay, and small animal imaging experiments.

IRDye QC-1 is the first non-fluorescent (dark) quencher, compatible with a wide range of visible and near-infrared fluorophores (~500 – 800 nm).

IRDye® Click Chemistry reagents (DBCO, Alkyne, and Azide) offer convenient, versatile and reliable methods for biomolecule labeling. With a variety of in vitro and in vivo applications, from biomarker isolation to assay development.

IRDye Infrared Dyes and near-infrared (NIR) fluorescent imaging deliver enhanced sensitivity due to low background autofluorescence in the near-infrared region, therefore, giving a higher signal to noise ratios.

Detection of binding partners for 100 different glycans in purified proteins, serum, plasma, cell culture supernatants, cell/tissue lysates or other body fluids.

IRDye Labeling Kits come in 3 forms and allow you to label your own peptides, antibodies, or proteins.

The RayBio® COVID-19 Spike-ACE2 binding assay kit is a rapid, simple, and sensitive method to characterize the binding affinity of the SARS-CoV-2 Spike (S) protein and the Angiotensin I Converting Enzyme 2 (ACE2) receptor complex in the presence of potential inhibitors.

Single molecule array (Simoa) testing is a protein detection technique that is orders of magnitude more sensitive than standard sandwich based immunoassay techniques. Traditional ELISA measurements are limited to pg/ml levels of detection. The RayBio Ultrasensitive Simoa Testing Services can achieve sensitivity as low as femtogram (fg/ml) levels, allowing the quantification of biomarkers at concentrations previously difficult…

The RayBiotech Monkeypox Virus 1-Step High Throughput PCR Kit is a ready to use PCR assay for the detection of monkeypox virus (MPXV) DNA. The 1-Step Nucleic Acid Stabilization Buffer eliminates the need for DNA extraction and purification steps.

Detection of binding partners for 300 different glycans in purified proteins, serum, plasma, cell culture supernatants, cell/tissue lysates or other body fluids.

RayBio® Lectin Array 95. Detects glycan profiles using 95 lectins. Suitable for all liquid sample types.

RayBio® Lectin Array 70. Detects glycan profiles using 70 lectins. Suitable for all liquid sample types.

IRDye 680LT dye is highly soluble in water and is significantly brighter and more photostable than many other 700 nm near-infrared dyes.

ZeptoMetrix® partners with assay developers across all stages of assay development, from concept and design to commercialization.

Multiplate live-cell analysis system

Cell-permeant probes for imaging the microtubule cytoskeleton in live cells. Available with blue, green, or far-red fluorescence.

A photo-reactive DNA-binding dye typically used in viability PCR (v-PCR) of microorganisms like bacteria, viruses, and fungi.

AntiFix™ Universal Antigen Retrieval Buffer provides excellent heat unmasking for a wide variety of targets at neutral pH, reducing the need for buffer optimization.

Fluorescent CF® Dye tyramides are used for tyramide signal amplification (TSA) for increasing immunofluorescence sensitivity in multicolor immunocytochemistry (ICC), immunohistochemistry (IHC), or in situ hybridization (ISH).

Far-red, mitochondrial stain with excellent tolerance for fixation and permeabilization after staining.

Preservative-free Annexin V conjugates are compatible with real-time staining of apoptotic cells for live cell imaging, fluorescence microscopy, or flow cytometry.

LysoView™ fluorescent dyes label lysosomes in live cells without a wash step, and are available in multiple colors with options for super-resolution imaging.

Label your antibody with one of our superior CF ®  Dyes in 15 minutes without a purification step. Labeling tolerates many common buffer components including BSA and ascites.

This unique reagent quenches lipofuscin autofluorescence in tissue sections for immunofluorescence staining and can also help to reduce autofluorescence from other sources like extracellular matrix.