High efficiency, low toxicity
transfection reagent for mRNA
and long RNA.
mRNA into a variety of cells
Used to directly transfect the
protein itself into mammalian cells,
instead of transfecting DNA or
mRNA encoding the protein of
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.
In Vivo Transfection Reagents
Tissue targeted reagents for animal research.
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High-quality viral transduction
reagents can achieve reliable
production of viral vectors to carry
corrected genes into cells.
Polybrene-Based Virus Delivery
RNAi In Vitro
Efficient siRNA delivery is a key
process for studying the function
of endogenous genes through
RNAi interference in vitro.
CRISPR/Cas9 genome editing is a
technology that allows scientists to
modify the genome of a cell at a
RNAi and siRNA
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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