Examples of 'restriction enzyme analysis' in a sentence
Meaning of "restriction enzyme analysis"
Restriction enzyme analysis: This phrase refers to a technique used in molecular biology to analyze DNA or RNA by cutting the nucleic acid at specific recognition sites using restriction enzymes. This method helps in studying genetic sequences, identifying gene mutations, constructing recombinant DNA molecules, and conducting DNA fingerprinting
How to use "restriction enzyme analysis" in a sentence
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restriction enzyme analysis
Confirmation was done by restriction enzyme analysis and sequencing.
Restriction enzyme analysis of amplicon.
Plasmid was obtained and restriction enzyme analysis performed.
Restriction enzyme analysis.
Transformants were characterized by restriction enzyme analysis.
Restriction enzyme analysis revealed that all examined plasmids were recombinant.
Mutagenesis was confirmed by restriction enzyme analysis.
Restriction enzyme analysis was used to identify the approximate sizes of these clones.
Orientation of the promoter was confirmed by restriction enzyme analysis.
Restriction enzyme analysis of the polymerase chain reaction product enabled rapid distinction between the subspecies.
Both mutagenesis events were confirmed by restriction enzyme analysis.
Restriction enzyme analysis was used to compare the DNA inserts of the five recombinants.
The correct construct was identified by restriction enzyme analysis.
Sequence determination Restriction enzyme analysis of the cDNA subfragments is performed using standard procedures.
Colonies were picked and screened vía restriction enzyme analysis.
See also
restriction endonucleases
restriction enzyme
restriction enzyme cleavage
restriction enzyme digestion
Restriction enzyme analysis of DNA from CAV field isolates.
All sequences were confirmed by restriction enzyme analysis and sequencing.
Recombinants with the insert in the correct orientation were identified by restriction enzyme analysis.
Their physical structure was verified by restriction enzyme analysis and agarose gel electrophoresis.
Constructs with the correct orientation for expression were identified by restriction enzyme analysis.
Its physical structure was verified by restriction enzyme analysis and agarose gel electrophoresis.
The genome structures of recombinant viruses were confirmed by restriction enzyme analysis.
Positive clones were identified by restriction enzyme analysis and confirmed by double-stranded sequencing.
The relationships between inserts were established by restriction enzyme analysis.
Restriction enzyme analysis was performed to confirm the structure of p Syn 3.
The orientation of the fragment was determined by restriction enzyme analysis.
A further restriction enzyme analysis showed that at least 7 plasmids contained the same DNA fragment.
The presence of the plasmids was tested by restriction enzyme analysis.
DNA restriction enzyme analysis ( DNA mapping ) and vector construction is a fundamental aspect of molecular biology.
The orientation of the cassette was determined by restriction enzyme analysis.
The restriction enzyme analysis data for pLFA33 were as shown in Table 2.
These two clones appeared identical from restriction enzyme analysis.
Positive clones were identified by restriction enzyme analysis and sequence verified generating vector JNW759.
The insert and its orientation were checked by restriction enzyme analysis.
The cloned fragments were identified by restriction enzyme analysis and Southern blot analysis.
All transformants were checked for the presence of the appropriate plasmid by restriction enzyme analysis.
Actually, it 's an audio book on restriction enzyme analysis and DNA typing.
The correct clones were identified by isolating plasmid DNA followed by restriction enzyme analysis.
Bacterial clones were analyzed further by restriction enzyme analysis and DNA sequencing.
The polymerase chain reaction product could be verified by restriction enzyme analysis.
The desired mutations were confirmed vía restriction enzyme analysis and DNA sequence analysis.
The genetic information for EF on the recombinant bacteriophages was localized using restriction enzyme analysis.
Figs . 4A and 4B illustrate the sequencing and restriction enzyme analysis for the Arg to Gln substitution ;.
Plasmid DNA was isolated from ampicillin resistant colonies and subjected to restriction enzyme analysis.
The DNA fragment was verified by means of restriction enzyme analysis and sequencing.
The proper size and orientation of the pADH insert were confirmed by restriction enzyme analysis.
The DNA is isolated and analyzed usually by restriction enzyme analysis and . or sequencing.
The plasmids from both positive clones were then subjected to restriction enzyme analysis.
The structure of S-PRV-159 was confirmed by restriction enzyme analysis with BamHI and XbaI.
Plasmid DNA was prepared and the plasmids were subjected to restriction enzyme analysis.
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