Examples of 'separated by electrophoresis' in a sentence

Meaning of "separated by electrophoresis"

separated by electrophoresis - a technique used in laboratories to separate macromolecules such as DNA, RNA, or proteins based on their size and charge by applying an electric field to move them through a gel matrix

How to use "separated by electrophoresis" in a sentence

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separated by electrophoresis
The fragments are separated by electrophoresis on an agarose gel.
The matrix was washed and samples were finally separated by electrophoresis.
Ten microlitres were separated by electrophoresis on agarose gels.
Briefly mRNA from numerous tissues was loaded onto gels and separated by electrophoresis.
Reaction products were separated by electrophoresis and analyzed by autoradiography.
The obtained plasmids were resolubilized in TE buffer and separated by electrophoresis.
The reaction products were separated by electrophoresis on an agarose gel.
Following transcription and translation of the PCR products, the polypeptides are separated by electrophoresis.
The other PstI fragments are separated by electrophoresis on agarose gel.
RNAs were separated by electrophoresis on 1 % formaldehyde gels and transferred to Genescreen membranes.
The centrifuged samples are then separated by electrophoresis.
The protein bands separated by electrophoresis are visualized by silver staining.
Once cut, the DNA fragments are separated by electrophoresis.
The protein bands separated by electrophoresis are visualized by silver or comassie staining.
The method of claim 6 wherein the product of step ( b ) is separated by electrophoresis.

See also

Products were separated by electrophoresis on denaturing polyacrylamide slab gels and counted.
The restriction fragments are then separated by electrophoresis and blotted.
The protein separated by electrophoresis was electrically transferred to polyvinylidene fluoride membranes.
Cellular proteins were separated by electrophoresis.
The sample was separated by electrophoresis under non-reducing conditions, in the absence of dithiothreitol ( DTT ).
The restriction fragments obtained were separated by electrophoresis on 1 % agarose gel.
The protein was separated by electrophoresis in accordance with the general procedure described above.
Newly synthesized radiolabelled proteins were produced and subsequently separated by electrophoresis on a 15 % SDS-polyacrylamide gel.
The samples are separated by electrophoresis and visualized using an ultraviolet light source.
The samples were loaded onto a 15 % SDS-polyacrylamide gel and the proteins were separated by electrophoresis.
A fraction of each faction can be separated by electrophoresis on a polyacrylamide gel.
The amplified DNA fragment, which is named the reaction product 6, is separated by electrophoresis.
Labeled products were separated by electrophoresis on a denaturing polyacrylamide gel and visualized by autoradiography.
The steps in proteomic analysis . ( a ) Cutting of gel strips containing targeted proteins separated by electrophoresis.
The amplificates are separated by electrophoresis and assessed with regard to quantity and quality.
After 10 min, the cells were lysed and the cellular proteins separated by electrophoresis ( SDS PAGE ).
The protein can be separated by electrophoresis in accordance with the general procedure described above.
PCR products thus produced were separated by electrophoresis on agarose gel.
PCR products were separated by electrophoresis on agarose and transferred onto charged nylon membranes.
The amplified DNA fragment is then separated by electrophoresis as described above.
The PCR products were separated by electrophoresis on a 5 % polyacrylamide sequencing gel and visualized by autoradiography.
Two resulted PCR products were separated by electrophoresis and eluted from gel.
The proteins were separated by electrophoresis on 10 % polyacrylamide gel and transferred onto a PVDF membrane.
The resulting fragments were then separated by electrophoresis on a 1 % agarose gel.
HDL cholesterol was separated by electrophoresis on agarose gels ( Chol / Trig Combo, Helena Laboratories ).
Upon completion, the reaction products are separated by electrophoresis on polyacrylamide gels.
They are separated by electrophoresis on 15 % polyacrylamide gel.
Viral RNA was isolated and separated by electrophoresis on a formaldehyde gel.
PCR products were separated by electrophoresis and analyzed by autoradiography.
The PCR reaction mixtures were then separated by electrophoresis on a 1 % agarose gel.
The proteins were then separated by electrophoresis on polyacrylamide gel under 10 % denatured conditions.
The resulting DNA fragments were size separated by electrophoresis on a 1.0 % agarose gel.
The PCR products were separated by electrophoresis in a 1.8 % agarose gel and were later quantified.
The PCR products are denatured in 50 % formamide and separated by electrophoresis in a 6 % nondenaturing polyarylamide gel.
RNA samples were separated by electrophoresis of 15 µg aliquots in a 1 % agarose-formaldehyde gel.

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