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Abbkine LDH Cytotoxicity Assay Kit provides a simple and easy colorimetric assay for the study of cytotoxicity. This assay is based on the reduction of the tetrazolium salt MTT in a NADH-coupled enzymatic reaction to a reduced form of MTT which exhibits an absorption maximum at 565 nm.
This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-mouse sICAM-1 antibodies are precoated on a high-affinity ELISA plate. Standard samples, test samples, and biotinylated detection antibodies are added to the wells of the ELISA plate. After incubation, sICAM-1 present in the samples binds to the solid-phase antibodies and the detection antibodies.
This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-mouse sVCAM-1 antibodies are precoated on a high-affinity ELISA plate. Standard samples, test samples, and the detection antibody labeled with horseradish peroxidase are added to the wells of the ELISA plate.
Reagent for total RNA extraction from cells or tissues.
The BCA Protein Assay Kit is developed based on the BCA method, one of the two most widely used protein quantification techniques in the world. It enables simple, highly stable, sensitive, and compatible protein concentration measurements.
Cleavage Under Target & Tagmentation (CUT&Tag®) is an emerging technique for studying DNA-protein interactions. The core of CUT&Tag® relies on Tn5 transposase fused to protein A/G. This fusion protein binds to an antibody via protein A/G, thereby tethering Tn5 near the target sites. The tethered Tn5 then performs targeted DNA cleavage and tagmentation, simultaneously introducing sequencing adapters required for next-generation sequencing (NGS). The resulting DNA fragments are extracted and amplified by PCR, generating a sequencing-ready library without additional fragmentation or end-repairing steps
MobaXterm is your ultimate toolbox for remote computing. In a single Windows application, it provides loads of functions that are tailored for programmers, webmasters, IT administrators and pretty much all users who need to handle their remote jobs in a more simple fashion.
Modular multimode microplate reader, with monochromator-based optics and filter-based optics for fluorescence and luminescence detection, plus filter-free UV-Vis absorbance. Synergy H1 offers continuously variable bandwidth monochromators for fluorescence excitation and emission wavelength selection. The bandwidth can be set between 9 and 50 nm, in 1 nm increments, to fully optimize reader settings for best sensitivity and specificity compared to fixed bandwidth systems.
LABO is an experiment design tool that researchers can use for creating 2D/3D stimulus presentation tasks on desktop, mobile, and Extended Reality (XR) devices.
PanScan is a computational tool that offers advanced capabilities for identifying novel sequences, SVs, and repetitive regions. With its ability to annotate duplicate genes and visualize complex genomic landscapes, PanScan provides invaluable insights into genetic diversity.
This original version of the Ultra™ RNA Library Prep Kit enables non-directional RNA library preparation in a streamlined workflow. However, we now recommend use of the more recent NEBNext Ultra II RNA Library Prep Kit for Illumina (NEB #E7770), which has been further optimized to provide increased yields of high quality libraries from a broader range of input amounts.
High ALDH expression has been reported for normal and cancer precursor cells of various lineages. The ALDEFLUOR assay is a widely published non-immunological method for the detection of ALDH-bright (ALDHbr) cells and can be used to detect cancer cells in hematopoietic, mammary, endothelial, mesenchymal, neural, and other tissues.
Reliability and innovation come together in Autostainer Link 48. Our trusted immunohistochemistry stainer is united with revolutionary software and connectivity options, delivering an outstanding level of integration that provides high productivity and efficient workflow.
Rapid 15 minute method for the isolation and purification of total RNA (including miRNA) from small input amounts of cultured animal cells, CTC, stem cells, immuno-sorted cells, and microdissected samples including laser-capture microdissection (LCM). The purified RNA is of the highest purity and integrity, and can be used in a number of qRT-PCR and digital PCR and other whole transcriptome applications.