Products & Reviews

The ultimate automated buffer exchange solution.

The only completely hands-free benchtop buffer exchange solution

The all-around LNP process developer

The most rapid viscometer out there

The unmatched lentivirus and exosome characterization tool

GenScript’s Enceed™ T cell Activation Reagent is a biocompatible, non-toxic solution designed for the in vitro activation and expansion of human T cells from PBMCs or enriched T cell populations. Utilizing nanosized particles coated with anti-CD3 and anti-CD28 antibodies, it ensures high-fold expansion with a stable memory phenotype, maintaining high cell viability for enhanced downstream applications.

4BD Gene-to-Plasmid service for $89 FLAT per construct

Accelerate precision gene editing with GenScript's custom synthetic crRNA for Cas12a(cpf1) projects.

As a pioneer in the CGT field, GenScript has developed the CytoSinct™ cell isolation platform and Enceed™ T Cell Activation reagents, leveraging its extensive experience in antibody and magnetic bead development, along with its comprehensive expertise in the CGT industry chain. We provide​ high-quality cell isolation magnetic nanobeads, activation reagents, consumables and instruments to accelerate the R&D and commercializatio…

High-quality and cost-effective custom RNA oligos up to 266 nt, featuring comprehensive modifications.

E. coli–based cell-free platform with 5BD TAT from sequence to protein.

Accelerate precision gene editing with GenScript's custom synthetic pegRNA for prime editing projects.

Unlock precision gene editing with GenScript’s complete Cas protein solutions. Explore our ready-to-use Cas9, Cas12a, Cas13a, Base Editors, MAD7, and Prime Editors- engineered for high efficiency, low off-target rates, and broad cell type compatibility. Licensed from Broad Institue, these products are available in both RUO and cGMP formats, and succesfully supported global IND applications. Need unique Cas nuclease or editors?…

siRNA/ASO services include design, synthesis, delivery, analysis, screening, and validation.

Accelerate precision gene editing with GenScript's custom synthetic gRNA for base editing projects.

GenScript provides lipid nanoparticle (LNP) formulation services for efficient delivery of nucleic acids and other therapeutic payloads across a wide range of research applications, including gene editing, vaccines, immunotherapy, and cell engineering. Leveraging expertise in payload synthesis and LNP formulation, GenScript supports the development of customized delivery solutions, including advanced targeted and novel LNP sys…

GenScript provides research-grade lentiviral vector (LVV) packaging services for gene delivery, cell engineering, and therapeutic research applications. Leveraging optimized packaging systems and integrated workflows, GenScript delivers high functional titer lentiviral vectors with fast turnaround times, including reliable packaging support for large insert constructs.

A ready-to-use, high-yield E. coli-based cell-free protein synthesis system.

GenScript provides targeted lipid nanoparticle (LNP) formulation services for precision RNA delivery applications, including immune cell engineering, in vivo CAR-T, gene editing, and therapeutic development. By combining optimized LNP formulations with ligand-mediated targeting strategies, the GenScript platform is designed to improve delivery efficiency, targeting specificity, and translational potential for advanced RNA ther…

CRISPR have been adapted as a powerful tool for genetic modification of the target host genome research, screening, and modeling. GenScript CRISPR cell line service leveraging industry leading capability in CRIPSR technology to provide one stop solution of cell line development from design to characteizatin, frequent project monitoring and updating, scalable capability of high-throughput cell line generation, high success rate…

11 Weeks from Antigen to Antibody – High-quality, Speed, and Reliability Delivered

5 Business Days from Gene to Antibody – Say Goodbye To Waiting

Custom mRNA synthesis from Gene-to-mRNA in 2 weeks

Ready-to-use mRNA, saRNA, circRNA & LNP delivered in 5 days

Comprehensive mRNA Analytical Services ensuring the quality, safety, and efficacy of your mRNA align with USP guidelines