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MICROFLUIDIC ELECTROPHORESIS-MEDIATED CHARACTERIZATION OF PLASMID DNA ISOFORMS

发明专利审中
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16权利要求 · 2 独立
§ Ⅰ

卷宗概要

发明人

Dipti Rasiklal MEHTA; James WHITE; Menel BEN FREJ; Shreyas SHAH; Lloyd BWANALI

IPC 分类

G1N 27/447G1N 21/64

CPC 分类

G1N27/44726G1N21/6486G1N27/44791

Methods of assessing double-stranded plasmid DNA isoforms to determine a proportion of supercoiled plasmid DNA compared to linear plasmid DNA, and/or open circle plasmid DNA are provided according to aspects of the present disclosure, which include: preferentially labelling double-stranded plasmid DNA; flowing the labeled double-stranded plasmid DNA through a polymeric separation medium in a microchannel into a detection region; detecting the detectable label to determine: a) an amount of time taken by the labeled plasmid DNA isoforms to flow through the polymeric separation medium in the microchannel into the detection region, and/or b) strength of the signal of the detectable label in the detection region; and comparing a) and/or b) to a reference standard thereby determining a proportion of supercoiled plasmid DNA compared to linear plasmid DNA, and/or open circle plasmid DNA in the fluid sample comprising plasmid DNA.

原文(中文)

Methods of assessing double-stranded plasmid DNA isoforms to determine a proportion of supercoiled plasmid DNA compared to linear plasmid DNA, and/or open circle plasmid DNA are provided according to aspects of the present disclosure, which include: preferentially labelling double-stranded plasmid DNA; flowing the labeled double-stranded plasmid DNA through a polymeric separation medium in a microchannel into a detection region; detecting the detectable label to determine: a) an amount of time taken by the labeled plasmid DNA isoforms to flow through the polymeric separation medium in the microchannel into the detection region, and/or b) strength of the signal of the detectable label in the detection region; and comparing a) and/or b) to a reference standard thereby determining a proportion of supercoiled plasmid DNA compared to linear plasmid DNA, and/or open circle plasmid DNA in the fluid sample comprising plasmid DNA.