Ví dụ về việc sử dụng Gel electrophoresis trong Tiếng anh và bản dịch của chúng sang Tiếng việt
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Gel electrophoresis and automated DNA sequencing(at UoS).
Look… we separated her DNA and mapped it using gel electrophoresis.
Agarose gel electrophoresis is the routine method for resolving DNA in the laboratory.
To evaluate the fragmentation effects on the genomic DNA,samples were analyzed by using agarose gel electrophoresis.
Formaldehyde is also used as a detergent in RNA gel electrophoresis, preventing RNA from forming secondary structures.
The first step in a western blotting procedureis to separate the macromolecules in a sample using gel electrophoresis.
The gel electrophoresis step is included in western blot analysis to resolve the issue of the cross-reactivity of antibodies.
Apoptotic cells(DNA fragmentation, an apoptotic catachrestic)were found after ESE treatment by TUNEL assay and DNA gel electrophoresis.
It uses gel electrophoresis to separate native proteins by 3-D structure or denatured proteins by the size of the polypeptide.
Taenia solium eggs and proglottids found in feces, ELISA,or polyacrylamide gel electrophoresis diagnose only taeniasis and not cysticercosis.
The technique uses gel electrophoresis to separate native proteins by 3-D structure or denatured proteins by the length of the polypeptide.
Allele specific oligonucleotide(ASO) is a technique that allows detection ofsingle base mutations without the need for PCR or gel electrophoresis.
Agarose gel electrophoresis was used to determine the size distribution of DNA subjected to post-extraction ultrasonic fragmentation(Fig. at the top right side).
It can also be used to separate large protein,and it is the preferred matrix for the gel electrophoresis of particles with effective radii larger than 5-10 nm.
Proteins can also be separated on the basis of size by using an SDS-PAGE gel, or on the basis of size andtheir electric charge by using 2D gel electrophoresis.
These include use in wastewater treatment, gel electrophoresis(SDS-PAGE), papermaking, ore processing, tertiary oil recovery, and the manufacture of permanent press fabrics.
In 1959, the groups of Davis and Ornstein and of Raymond andWeintraub independently published on the use of polyacrylamide gel electrophoresis to separate charged molecules.
Proteins are commonly separated using polyacrylamide gel electrophoresis(PAGE) to characterize individual proteins in a complex sample or to examine multiple proteins within a single sample.
In additional experiments, they treated pure collagen with hydrogen peroxide andthen analyzed the protein using a gel electrophoresis laboratory technique that allows the protein to be visualized.
Proteins can be separated on the basis of size by using an SDS-PAGE gel, or on the basis of size andtheir electric charge by using what is known as a 2D gel electrophoresis.
These efforts started with two-dimensional gel electrophoresis[1] efforts in the 1970s and in more recent times this research has been performed using LC-tandem MS[2][3][4] based proteomics.
In cases of human cysticercosis, diagnosis is a sensitive problem and requires biopsy of the infected tissue or sophisticated instruments.[1] Taenia solium eggs and proglottids found in feces, ELISA,or polyacrylamide gel electrophoresis diagnose only taeniasis and not cysticercosis.
Quantitative preparative native continuous polyacrylamide gel electrophoresis(QPNC-PAGE) is a new method for separating native metalloproteins in complex biological matrices.
They also verified that the daughter rings were a result of annealing to the single-strand toeholds from the initial ring rather than as a result of self-assembly ofresidual DNA motifs in solution using gel electrophoresis and extracting the DNA products from each phase.
Using a specialist process called 2D gel electrophoresis, the scientists separated out all the proteins found within the mitochondria of brain cells and muscle cells from normal young brains and normal middle-aged brains and compared the two samples.
Cell debris were removed by centrifugation(6000× g, 4°C, 5 min) and analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE) under reducing conditions according to the method of Laemmli(1970) with 12.5% polyacralamide gels. .
After subjecting samples to ultraviolet light,the scientists pulled their DNA apart in electrophoresis gel(a traditional DNA analysis tool).
However low-concentration gels(0.1- 0.2%) are fragile and therefore hard to handle, and the electrophoresis of large DNA molecules can take several days.