Transfection Reagents

OUR PRODUCTS

RNA/mRNA Delivery In Vitro

High efficiency, low toxicity transfection reagent for mRNA and long RNA.

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Protein Transfection

Used to directly transfect the protein itself into mammalian cells, instead of transfecting DNA or mRNA encoding the protein of interest.

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Gene Expression

Using BOC Sciences DNA transfection reagents can achieve higher efficiency of genomic expression, and avoid cytotoxicity, to help study the function of the target protein, and its role in the cell signal transduction pathway.

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Virus Production

High-quality viral transduction reagents can achieve reliable production of viral vectors to carry corrected genes into cells.

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RNAi In Vitro

Efficient siRNA delivery is a key process for studying the function of endogenous genes through RNAi interference in vitro.

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CRISPR Gene Editing

CRISPR/Cas9 genome editing is a technology that allows scientists to modify the genome of a cell at a specific location.

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TRANSFECTION METHODS

Liposome-mediated Transfection

Effectively transferring foreign genetic material to cells for expression and functional research is a basic technique in modern cell biology. Specially designed lipid-based transfection reagents can promote the transportation of DNA, mRNA, siRNA into cells. Lipids with an overall net positive charge at physiological pH (Cationic) are the most common synthetic lipid component of liposomes developed for gene delivery.

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Liposome-mediated Transfection

RNAi and siRNA Transfection

RNAi technology can be used to assess the function of many genes in the genome that may be related to the disease. It provides an effective means of blocking the expression of specific genes and evaluating their chances of compounds or signaling pathways.

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RNAi and siRNA Transfection

WHY CHOOSE US

BOC Sciences is committed to providing innovative nucleic acid and protein transfection solutions to meet customer needs at a reasonable price. With high-quality chemical transfection reagents, electroporation products, and virus production and transduction products, we can now provide the best delivery system for life science research, gene therapy, and cell therapy.