Gene editing therapy paves way for revolution in treatment of genetic disorders
It is hoped this therapy will be a breakthrough for patients suffering from hereditary transthyretin (ATTR) amyloidosis
It is hoped this therapy will be a breakthrough for patients suffering from hereditary transthyretin (ATTR) amyloidosis
Population genetics sequencing panel incorporates global genetic variations for superior study of disease and target discovery
Leading clinical laboratory runs first-ever successful automation of a CRISPR test for high-throughput, using Sherlock’s SARS-CoV-2 process
Study finds switches near GDF5 gene linked to knee osteoarthritis, hip dysplasia
EPISEQ SARS-COV-2 will support microbiology labs in identification and reporting from raw sequencing data related to SARS-CoV-2 variants
Solutions to complement Company’s growing position in cell and gene therapy research and development
Solutions combine liquid-based sample preparation with PCR detection and Sanger sequencing
Explore topics from live-cell analysis, in situ hybridization, cancer therapeutics, cell imaging, and much more
License agreement to enhance GenScript’s CRISPR offering for gene and cell therapy research
Discover how collaborative research between big pharma and academia is using the latest proteomics platforms to revolutionize drug discovery
Explore topics from LC-MS for oligos, peptides, glycans, and large molecule characterization to 3D cell culture for anticancer therapies
KSQ Therapeutics uses technology created at MIT to study the role of every human gene in disease biology
New, reversible CRISPR method can control gene expression while leaving underlying DNA sequence unchanged
Explore topics from AAV gene therapy and food fraud advances to LC-MS and Raman spectroscopy for drug discovery
Reserve your place today for talks on topics ranging from food fraud, spatial infiltration and CRISPR to antibody and AAV gene therapies