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Are there any limitations
with your current transfection method?
My titers are so low, that I can not make enough protein to evaluate
or I have to run a lot of transfections.
My transfection method works only with HEK cells, which is not my manufacturing cell line.
I have batch-to-batch variations with my transfection reagent so I have problems with reproducibility.
My current method is not scalable.
My current method gives poor efficiency with difficult-to-transfect cells.