Search results for "ffpe challenges"

Examine the benefits and logistics of transitioning your program from traditional site-based blood collection to remote sampling

Explore innovations such as oligonucleotide therapeutics, bi-specific antibodies, CAR-T therapy and CRISPR

BMG LABTECH shares the importance of having a fit-for-purpose microplate reader and introduces its latest technology, the VANTAstar

Genome editing experts harness the power of CRISPR-Cas enzymes to power the next diagnostic revolution in COVID-19 detection and diagnosis

Explore topics from perfume profiling, salmonella spp. detection, regulatory biopharma compliance, and in situ hybridization

Conjugate chemistry pioneer Dr. Andrew Lees reveals the cutting-edge freezer technology that made all the difference in his lab

A new study provides important insights into patterns of antibiotic resistance (ABR) and how they vary widely in different river systems

Find out how CLINICAL24 Ambassador, Dr. Frank Peacock, is advancing cardiovascular care through clinical trials in acute coronary syndrome and heart failure, driving progress in emergency medicine

Optimized for maximum recovery and sensitive DNA variant detection

The Agilent SurePrint G3 ISCA v2 CGH 4x180K Microarray dual-color chromosomal microarray contains 60-mer high-quality probes. The ISCA CGH microarray is an effective tool for targeted genome-wide DNA copy number variation profiling without reducing amplification or complexity.

The SurePrint G3 ISCA v2 CGH 8x60K dual-color chromosomal microarray contains 60-mer high-quality probes. The ISCA CGH microarray is an effective tool for targeted genome-wide DNA copy number variation profiling without amplification or complexity reduction.

ThruPLEX DNA-seq Kit—General Purpose Library Preparation for Illumina NGS Platforms

Easy to use and fast tissue homogenizer and cell lyser for efficient and reproducible sample preparation 

Supporting earlier Alzheimer's disease diagnosis

Stanford University researchers reproducibly grew clinical-grade iPSC’s in search of a new treatment for rare genetic disease