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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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Providing functional, high-purity recombinant proteins—including membrane proteins and nanodiscs—to overcome bottlenecks in drug screening and target validation.
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Ready-to-use clones for streamlined research and development.
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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.
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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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Effortlessly streamline DNA extraction with CB™ Magnetic-Nanoparticle Systems.
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Comprehensive solutions covering design, development, and validation to ensure conjugated drugs with consistent quality and clinical potential.
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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.
Nucleotides Service
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Custom synthesis of oligonucleotides, primers, and probes for gene editing, PCR, and RNA studies.
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Custom RNA ServicePrecise | Flexible | GMP-ReadyCustom
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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Complete biosafety testing solutions for gene therapy, viral vectors, and biologics development.
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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.
GMP mRNA Production
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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: 3' OMe refers to the 3' end modification of a nucleic acid molecule, typically RNA, with a methyl group (-CH3) at the 3' hydroxyl (-OH) position of the ribose sugar.
A: This is accomplished through a chemical synthesis method called solid-phase synthesis, where the 3' end of the RNA is modified with a 3'-O-levulinyl protecting group during oligonucleotide synthesis. After the RNA synthesis is completed, the 3'-O-levulinyl protecting group is removed, exposing the 3'-OH group, which can then be methylated using a methylating agent such as iodomethane.
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Great kit. T7 Cap1 (3' OMe) mRNA Synthesis Kit can produce large amounts of Cap 1- and N1-Methylpseudouridine-modified (m)RNA via in vitro transcription with T7 RNA polymerase.
United States
01/02/2021
The resulting 5’-capped (m)RNA can subsequently be used for microinjection, transfection or in vitro translation experiments. All-in-One T7 Cap1 (3' OMe) mRNA Synthesis Kit makes the operation more convenient.
United States
03/25/2022
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| Cat.No. | Product Name | Price |
|---|---|---|
| RSNK-024 | RNase Inhibitor, Murine | Inquiry |
| RSNK-010 | All-in-One T7 Cap1 (3' OMe) mRNA Synthesis Kit Plus I | Inquiry |
| RSNK-013 | m7G(5')ppp(5')G Cap Analog | Inquiry |
| RSNK-028 | T7 High Yield RNA Synthesis Kit (Low dsRNA) | Inquiry |
| RSNK-003 | Fluorescein RNA Labeling Kit (T7) | Inquiry |
| RSNK-016 | m7G(5')ppp(5')(2'OMeG)pG Cap Analog | Inquiry |
| RSNK-014 | m7G(5')ppp(5')(2'OMeA)pG Cap Analog | Inquiry |
| RSNK-018 | Pseudo-UTP | Inquiry |
| RSNK-001 | T7 High Yield RNA Synthesis Kit | Inquiry |
| RSNK-017 | m7(3'OMeG)(5')ppp(5')(2'OMeG)pG Cap Analog | Inquiry |
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