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Dna Library Equipment Supplied In North America
6 equipment items found
Manufactured by:Claret Bioscience based inSanta Cruz, CALIFORNIA (USA)
The SRSLY NGS Library Prep Kit provides a simple and efficient ligation-based single-stranded DNA library preparation method that is engineered to produce complex libraries from low inputs of degraded DNA in about 2.5 hours. The SRSLY PicoPlus Kit is particularly designed for improved retention of short dsDNA ...
by:Dyno Therapeutics based inWatertown, MASSACHUSETTS (USA)
Our CapsidMap™ platform uses AI to systematically and rapidly optimize AAV capsids, overcoming the limitations of naturally occurring virus capsids by improving targeting ability, payload size, immune evasion and manufacturability. By building a massive and detailed map of synthetic AAV capsid sequence space, we can quickly navigate the landscape to find enhanced gene therapy vectors with ...
by:AptaMatrix, Inc. based inSyracuse, NEW YORK (USA)
Aptamers are DNA/RNA molecules that have affinities for their targets similar to antibodies. Aptamers have shown great potential to replace antibodies in biosensors, point-of-care diagnostics, therapeutics, and all of the areas currently dominated by antibodies. Once aptamers have been identified, they can be produced for less than 10% of the cost of antibodies. The commercial value of antibodies ...
Manufactured by:EntroGen, Inc. based inWoodland Hills, CALIFORNIA (USA)
EntroGen NGS Targeted Hotspot Panel is a comprehensive pan-cancer assay designed to detect clinically relevant hotspot mutations in solid tumors. Utilizing a robust next-generation sequencing (NGS) platform, labs are able to simultaneously analyze several different tumor types by batching up to 12 samples on a single run*. NGS Targeted Hotspot Panel (THSP) is compatible with fresh frozen, and ...
Manufactured by:EntroGen, Inc. based inWoodland Hills, CALIFORNIA (USA)
BRCA Complete Expanded Panel is a complete next generation sequencing (NGS) solution for detecting clinically relevant BRCA1 and BRCA2 mutations along with extended coverage of CHEK2, PALB2, RAD51C and TP53. ...
by:Gene Codes Corporation based inAnn Arbor, MICHIGAN (USA)
Sequencher empowers the benchtop scientist by bringing the latest peer-reviewed NGS algorithms out of the command line and into an intuitive point and click interface. Whether performing reference-guided alignments, de novo assembly, variant calling, or SNP analyses, Sequencher has the tools you need to get results. Sequencher has integrated the comprehensive Cufflinks suite for in-depth ...