We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms
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.
cloud-based flow cytometry analysis platform bridging machine learning and analytical pipelines with classical analysis
A Probabilistic Genome Simulator for Non-uniform Simple, Canonical, and Complex Structural Variations to Facilitate Benchmarking
for RNA, miRNA extraction
eNRSA is an enhanced version of NRSA for analyzing nascent transcription profiles generated by PRO-seq, GRO-seq, (m)NET-seq, and Butt-seq data.
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