GenScript Biotech Corporation (HK.1548) is the world’s leading technology and service provider of life science R&D and manufacture. Built upon its solid gene synthesis technology, GenScript Biotech is divided into four major platforms including the life science service and product platform, the biologics contract development and manufacturing organization (CDMO) platform, the industrial synthetic products platform, and the integrated global cell therapy platform.
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* As of June 30th, 2023
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As the leading gene synthesis provider in the world, our gene synthesis tools are designed to make research accessible. Our propriety, population immune algorithm based GenSmart codon optimization technology enables the design of the most expression-efficient sequence available, while our CloneArk™ system provides a platform for researchers to archive, share and reuse their clones for future use with peace of mind.
Powered by advanced PepPower™ synthesis technology platform and supported by stringent quality management systems, GenScript synthesizes more than 25,000 peptides/month, featured with variety of custom modifications, delivery options, and high level of batch-to-batch consistency
Powered by a unique B-cell cloning protocol, GenScript allows our clients to test for antibodies that work in their application before sequencing the desired clones for recombinant antibody production. Work with us to generate exclusive, custom rabbit monoclonal antibodies that are high in sensitivity, affinity and specificity for your research and diagnostic needs.
Designed to accelerate the drug screening process, GenScript helps researchers identify promising candidate leads and advance to the production of purified recombinant antibodies with one of the fastest turnaround times in the industry.
Through partnership with the technology's pioneering Broad Institute of MIT and Harvard, as well as ERS Genomics, GenScript offers a variety of CRISPR services, including guide RNA design tools, pre-validated CRISPR plasmids, and learning resources to help scientists harness the power of CRISPR genome editing in life science research.