Examples of 'acrylamide gel' in a sentence

Meaning of "acrylamide gel"

Acrylamide gel: A substance used in gel electrophoresis to separate and analyze proteins or nucleic acids based on their size and charge. It is commonly used in laboratory settings for DNA profiling, genetic research, and protein analysis

How to use "acrylamide gel" in a sentence

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acrylamide gel
The complexes were resolved on an acrylamide gel.
An acrylamide gel is used to separate the remaining protected fragments.
The complexes are resolved by means of electrophoresis on an acrylamide gel.
Amplification products were separated on an acrylamide gel and stained with ethidium bromide.
The remaining protected fragments are separated on an acrylamide gel.
This dsRNA is resolved further by acrylamide gel electrophoresis into three closely spaced bands.
To test the efficiency of tailing the products were run on an acrylamide gel.
The digest fragments were purified by native acrylamide gel electrophoresis followed by gel filtration chromatography.
Proteins contained within this concentrate were then resolved on an acrylamide gel.
This is an acrylamide gel containing specific antibodies to the lipoprotein Lpa.
Samples were then analyzed by silver stained acrylamide gel electrophoresis.
Acrylamide gel electrophoresis of DNA was done as described by Maniatis, et al.
The streptavidin complexes are recovered by centrifugation and electrophoresed on an acrylamide gel.
RNAs were separated according to their size by acrylamide gel electrophoresis and gel extracted.
Denatured protein samples were stored on ice until loading on to the acrylamide gel.

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The eluted proteins were separated by acrylamide gel electrophoresis and stained with Coomassie Blue.
The proteins present in the samples are then separated by means of acrylamide gel electrophoresis.
The acrylamide gel exclusion column was from Beckman Instruments, Fullerton, Calif.
The formation of polyion complexes was examined by acrylamide gel shift assay.
A 5 % acrylamide gel is prepared using techniques known in the art.
The purity and integrity of the oligonucleotide preparation was determined by acrylamide gel electrophoresis.
These are estimates derived from agarose or acrylamide gel electrophoresis or from published DNA sequences.
This results from the fact that the degenerated oligonucleotides were purified on acrylamide gel.
The PCR product was electrophoresed in a 6 % acrylamide gel and analyzed by autoradiography.
Glycine content was high due to some carryover from the buffer within the acrylamide gel.
On completion of electrophoresis, the acrylamide gel was stained with Coomassie Blue.
The DNA was digested with BamHI to completion and purified on an acrylamide gel.
Briefly, a non-denaturing acrylamide gel is loaded with samples.
After transcription, the RNAs are purified on denaturing acrylamide gel.
Samples were subsequently analyzed by a 4 % acrylamide gel electrophoresis, and homochromatography analysis.
Genetic polymorphisms were identified from polymorphism between individuals sampled, detected by electrophoresis on acrylamide gel 8.
Fifteen µl of sample was used for SDS acrylamide gel electrophoresis.
A 10 % acrylamide gel was run to confirm the identity of the purified fraction.
Refolded forms were detected by semi-native poly acrylamide gel electrophoresis.
An 8 % acrylamide gel is conventionally used for detecting the different forms of A / C-type lamins.
After digestion, the resulting fragment mixture was subjected to acrylamide gel electrophoresis.
Fig . 2 A shows a denaturing ( SDS ) acrylamide gel on completion of electrophoresis stained with Coomassie Blue.
Figure 13 shows biological activities of material eluted from bands in acrylamide gel electrophoresis.
A 13 % acrylamide gel was used and stained with silver.
After having been boiled for 5 minutes, the proteins are loaded onto the acrylamide gel.
Supernatant from the 293T cells was run on an acrylamide gel and proteins transferred to a membrane.
The DNA was digested with BamH-I to completion and purified on a acrylamide gel.
The figure shows a 10 % acrylamide gel of representative PCR-generated inserts,.
Aliquots from the second round of PCR amplification were subjected to electrophoresis on a 5 % acrylamide gel.
The p Eco RI linker was removed by 5 % acrylamide gel electrophoresis.
The precipitates was dissolved in 20 µl of sterilized distilled water and electrophoresed on 5 % acrylamide gel.
The 120 bp fragment was then purified by acrylamide gel electrophoresis.
By SDS acrylamide gel and silver staining, the protein was better than 95 % pure.
The remaining portion of the PCR reaction mixture was therefore purified by 5 % acrylamide gel electrochromatography.
The upper stacking gel used 3 % acrylamide gel, the lower separating gel contained 14 % acrylamide gel.

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