Products, services, reviews and techniques used in the identification and validation of the disease-causing target genes and proteins.
The FluidX™ Aperio™ semi-automatic system is designed for efficient capping of 24, 48 or 96-format SBS racked tubes in labs with medium to high throughput. It offers the consistency of an automated decapping system, at lower price point.
Gene Pulser®/Micropulser™ electroporation cuvettes are high-quality electroporation cuvettes which enable reproducible and consistent gene delivery to valuable transfection samples.
Gene Pulser®/Micropulser™ electroporation cuvettes are high-quality electroporation cuvettes which enable reproducible and consistent gene delivery to valuable transfection samples.
30 slide pack of dual-chamber slides (60 counts), includes 1.5 ml trypan blue, for use with TC10™ or TC20™ automated cell counter
30 slide pack of dual-chamber slides (60 counts), each slide can provide counts for 2 separate samples or dilutions, for use with TC10™ or TC20™ automated cell counter
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.
PureBlu™ Nuclear Staining Dyes are designed to specifically stain the nuclei of cells in fixed and unfixed samples for fluorescence microscopy and cell imaging applications.
PureBlu™ Nuclear Staining Dyes are designed to specifically stain the nuclei of cells in fixed and unfixed samples for fluorescence microscopy and cell imaging applications.
Pkg of 100, bursts at 1,800 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
TransFectin reagent is a cationic lipid reagent that delivers the highest efficiencies and expression levels over a broad range of cell lines, including some difficult-to-transfect and primary cells, while minimizing damaging cytotoxic effects observed with other high-efficiency general transfection reagents.
Pkg of 100, bursts at 1,550 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
Pkg of 100, bursts at 1,100 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
siLentFect reagent is a high-efficiency cationic lipid developed for the transfection of cultured mammalian cells with short interfering RNA (siRNA). Effective delivery of the siRNA molecules is critical to the success of RNA interference (RNAi) applications.
Pkg of 100, bursts at 900 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
Pkg of 100, bursts at 650 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
Pkg of 100, bursts at 450 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
Pkg of 100, bursts at 1,350 psi in a partial vacuum, for use with the PDS-1000/He biolistic system (#165-2257, #165-2258)
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.
