Whole column high-throughput screening of mRNA AAV circular RNA porous plates

NegotiableUpdate on 05/07

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Overview

Optimization of buffer solution for in vivo car-t lentivirus on a 0.05 mL integral 96 well ClM QA plate by clarification harvesting. CIM oligonucleotide Oligo (dT) 0.05 mL integral 96 well plate was used to optimize mRNA process conditions

Product Details

in vivo car-tSlow virus inClM QA 0.05 mLmonolithic 96 Optimization of buffer solution by clarifying harvest on orifice plate

adoptCIMoligonucleotideOlive (DT) 0.05Milliliter integral96Orifice platemRNAOptimization of process conditions for oligonucleotidesOlive (DT)Perform multi-channel parallel screening based on the bonding conditions of the overall board. Identified the impactDBCThe three key factors are:NaClGlycoside acid hydrochloride andMgCl2.

Double combined capacity(DBC)for2-4 mg/mLThe load capacity depends onmRNASequence and length.

If usedGu-HClsubstituteNaClThe capacity can be significantly increasedThis article verifiesDBCThe value can reach>6 mg/mL.

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