Examples of 'acrylamide gels' in a sentence
Meaning of "acrylamide gels"
Acrylamide gels: Gels used in biochemical and molecular biology research for techniques such as electrophoresis to separate and analyze biomolecules based on their size and charge
How to use "acrylamide gels" in a sentence
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acrylamide gels
In vitro splicing products are analyzed on denaturing acrylamide gels.
Acrylamide gels were prepared using standard protocols and stained with silver stain.
Reaction products were separated on gradient acrylamide gels and autoradiographed.
Acrylamide gels are generally formed from an aqueous solution containing acrylamide monomer and photoinitiator.
This allows for low molecular weight proteins to be separated in lower percent acrylamide gels.
In particular, the cassette enables the use of acrylamide gels in horizontal electrophoresis.
In comparing the acrylamide gels either visually or optically, several electrophoretically specific bands were apparent.
Splicing complexes are electrophoresed on non-denaturing acrylamide gels and visualized by autoradiography.
Lower % T acrylamide gels can also assist in the sequencing of longer fragments.
The amplified cDNA was then loaded onto 5 % acrylamide gels and stained with ethidium bromide.
Subsequently, the ( digested ) PCR products were analysed by electrophoresis in agarose or acrylamide gels.
One µg of oncotoxin was resolved on 15 % acrylamide gels as described below.
Subsequently, the ( cleaved ) PCR products were analysed by electrophoresis in agarose or acrylamide gels.
The purified samples were loaded onto 10 % acrylamide gels and quantitated as before.
Under reducing conditions unfractionated H-gal-GP complex resolved into some 8 bands on 10 % acrylamide gels.
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The samples were electrophoresed on 5 % non-reducing acrylamide gels and blotted to immobilon membrane.
Precast 4-20 % acrylamide gels and broad range molecular weight markers were obtained from Bio-Rad Laboratories.
Radiolabeled transcripts were analysed on 4 % acrylamide gels.
Lysates were electrophoresed in 8 % acrylamide gels and blotted with anti-EGF-R antibody.
Samples were then applied to 12 % denaturing acrylamide gels.
The Fv fragment was also analysed on native acrylamide gels at pH 7.5.
The second dimension had been carried out on 10 % acrylamide gels.
Products were analyzed on 6 % acrylamide gels.
Different fractions are deposited on two SDS-page 15 % acrylamide gels.
Nevertheless the Fv fragment dissociated on native acrylamide gels at pH 4.5.
The PCR products were then separated using 6 % ( weight / v ) acrylamide gels.
The sequencing samples were analysed on wedge-shaped 6 % acrylamide gels containing 7 M urea.
Proteins were separated by SDS-PAGE in 8 % acrylamide gels.
Plasma or serum volumes equivalent to 1.5 µl were loaded onto 10 % acrylamide gels under non-reducing conditions.
Proteins from cell extracts were resolved by PAGE on 8.5 % SDS acrylamide gels.
The samples were then subjected to SDS-PAGE analysis on 10 % acrylamide gels.
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