Rhodamine Phalloidin Reagent ab235138 is one of a series of phalloidin conjugates that are used to stain actin filaments in fluoresence microscopy. The tetramethyl rhodamine dye can be easily detected with a fluorescent microscope at Ex/Em = 546/575 nm.
TiO 2 – functional microparticles for highly-specific phosphopeptide enrichment
Less interferences for even more confidence
Comprehensive nanoparticle analysis by nano-flow cytometry. The NanoAnalyzer offers a unique solution combining the physical characterization of nano-sized objects (10nm-1µm) together with the phenotyping of their biochemical properties. The platforms determine simultaneously the size, concentration, and sub-populations according to the surface or intraluminal markers. It is already used for extracellular vesicles, viruses, v…
Cell scraper, 2-position blade, size: L, handle length: 36 cm, blade length: 1.7 cm, sterile, non-pyrogenic/endotoxin-free, non-cytotoxic, 1 piece(s)/blister
High optical-quality glass bottom, black microplates are ideal for performing high content cell-based assays using imaging systems. The glass bottom provides a flat and optically clear surface that reduces autofocus time, increases throughput and is ideal for cell growth.
DISC™ devices give scientists enhanced control over growth factor levels in their cultures. Adding one DISC™ provides a stable level of native growth factors over 1-2 weeks. DISCs™ reduce your cell culture costs and provide robust, high-quality cells.
The FiberCell Systems Duet Pump provides flexible flow rate support for all of the FiberCell Systems hollow fiber bioreactor cartridges.
GTP Solution for Gyrolab provides sensitive immunoassay detection of residual endonuclease such as Benzonase Nuclease and Denarase in viral vector bioprocess samples.
HEK 293 HCP Solution for Gyrolab provides immunoassay detection of HEK 293 host cell protein (HCP) impurities in bioprocess and viral vector manufacturing samples.
Unlock the full potential of the BD FACSymphonyâ„¢ platform with the flexibility of spectral unmixing or compensation workflows
A high-throughput platform offering uncompromised data quality
ClonExpress ® technology is a simple, fast and efficient DNA seamless cloning technology, which can clone the insert into any position of any vector.Â
All-in-one, ready-to-use Cas9 and guide RNA (gRNA) expression plasmids for use with monocots and dicots.
CRISPR/Cas9-mediated recombineering is the most powerful bacterial genome engineering method to date. In addition, Cas9-mediated recombineering overcomes the dependence on a second recombination step, avoids the creation of destabilizing scar sites, can be used in multiplexing, and is less time-consuming than previous protocols.
This Lentiviral Packaging Mix is an optimized formulation of two plasmids expressing the key HIV packaging genes and a heterologous viral envelope gene.
Universal negative control CRISPRs have been designed not to recognize any sequence in the human, mouse or rat genome.Â
Compare and contrast the features of a wide variety of guide RNA (gRNA) and Cas9 products for in vitro and in vivo CRISPR experiments. Select the best formats for your mammalian or plant applications: SygRNA ® synthetic gRNA, plasmid DNA, lentiviral particles, and proteins.
An easy-to-use, modular platform to co-culture different cell types in discrete 3D and 2D compartments.
Exclusive human or mouse whole genome arrayed libraries developed with the Wellcome Sanger institute
Pooled CRISPR screening with 10x Genomics compatibility
for Latex Agglutination and Latex Turbidimetry Immunoassay
Choose standard KASP by Design (KBD) service for design and delivery of a KASP Assay to your SNP or indel of interest. It consists of three KASP primers that are specific to the SNP or indel of interest. Assay design (primer selection) is carried out using our proprietary Krakenâ„¢ software system. Â
Choose premier KASP on Demand (KOD) service for design and delivery of your KASP Assay, plus full validation and optimization of your assay by our scientific team. Â
Enzyme Immunoassay for the Quantitative determination of Protein L Ligand from medium containing immunoglobulin (Ig) or Ig-fragments. Accurate, robust results with a wider assay range, allowing for better quantification of the protein L contaminant.
