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Accelerate your research with cost-effective LncRNA qPCR Array Technology.
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Human Druggable Genome siRNA Library enables efficient drug target screening.
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Clones
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Chromogenic LAL Endotoxin Assay Kit ensures precise, FDA-compliant endotoxin quantification for biosafety testing.
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Powerful Tn5 Transposase for DNA insertion and random library construction.
Aptamers
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Aptamers for key proteins like ACVR1A, Akt, EGFR, and VEGFR.
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Enhance immune responses with high-purity, potent CpG ODNs.
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Unbeatable pricing, fully customizable viral packaging services (covering 30,000+ human genes, 200+ mammals, 50+ protein tags).
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Harness the power of protein degraders for precise protein degradation, expanding druggable targets and enhancing therapeutic effectiveness for cutting-edge drug discovery.
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RNA design, synthesis, and manufacturing—covering mRNA, saRNA, circRNA, and RNAi. Fast turnaround, rigorous QC, and seamless transition from research to GMP production.
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Custom cDNA, genomic, and mutagenesis libraries for drug discovery, screening, and functional genomics.
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Gene editing solutions for gene editing, knockouts, knock-ins, and customized genetic modifications. Integrated multi-platform solutions for one-stop CRISPR sgRNA library synthesis and gene screening services
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Enhance microbial productivity with advanced genome editing using Rec-mediated recombination and CRISPR/Cas9 technologies.
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Genetic modification for crop improvement, biotechnology, and plant-based research solutions.
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Plant-based protein expression systems for biopharmaceuticals, enzyme production, and research.
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Revolutionizing drug delivery and diagnostic development with next-generation high-throughput aptamer selection and synthesis technologies.
CGT Biosafety Testing
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Internationally certified evaluation system for biologics, gene therapies, nucleic acid drugs, and vaccines.
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Stable expression over 15 generations with rapid cell line development in just 3 months.
Supports adherent and suspension cell lines, offering MCB, WCB, and PCB establishment.
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Scalable mRNA production from milligrams to grams, with personalized process design for sequence optimization, cap selection, and nucleotide modifications, all in one service.
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Our plasmid production services span Non-GMP, GMP-Like, and GMP-Grade levels, with specialized options for linearized plasmids.
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Advanced platforms for AAV, adenovirus, lentivirus, and retrovirus production, with strict adherence to GMP guidelines and robust quality control.
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AI-powered one-click design for customized CRISPR gene editing strategy development.
AI-Antibody Engineering Fusion
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AI and ML algorithms accelerate antibody screening and predict new structures, unlocking unprecedented possibilities in antibody engineering.
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High-throughput enzyme activity testing with proprietary datasets and deep learning models for standardized and precise enzyme engineering design.
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Leverage AI to uncover hidden high-potential small molecules, prioritize leads intelligently, and reduce costly trial-and-error in early drug discovery.
AI-Driven Protein Degrader Drug Development
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Use AI-guided design to optimize protein degraders, addressing design complexity and enhancing efficacy while shortening development timelines.
A: Some plasmids (often called packaging and envelope plasmids) encode components of the viral capsid and envelope and are used in conjunction with plasmids encoding the viral genome (often called transfer plasmids).
A: About 9 kb.
A: The process of lentiviral packaging involves introducing a desired gene or RNA sequence into a modified lentiviral genome, which serves as the viral vector. This modified genome contains the necessary components for the vector to package the desired genetic material and deliver it to target cells.
A: Lentiviral packaging requires the transfection of three components into packaging cells: 1. A lentiviral transfer plasmid containing the insert of your interest; 2. A packaging plasmid that expresses all necessary viral structural proteins; 3. An envelope plasmid.
A: Lentiviruses have the ability to infect both dividing and non-dividing cells, allowing them to deliver genes to a wide range of cell types. This enables the targeting of specific cell types in gene therapy applications.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
These Lentivirus Packaging Kits come with user-friendly instructions and protocols, making them accessible to researchers with varying levels of expertise in virus packaging techniques.
United States
01/27/2022
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