After a DNA segment has been digested using a restriction enzyme, the resulting fragments can be examined using a laboratory method called gel electrophoresis, which is used to separate pieces of DNA according to their size.
Restriction mapping is a method used to map an unknown segment of DNA by breaking it into pieces and then identifying the locations of the breakpoints. This method relies upon the use of proteins called restriction enzymes, which can cut, or digest, DNA molecules at short, specific sequences called restriction sites. After a DNA segment has been digested using a restriction enzyme, the resulting fragments can be examined using a laboratory method called gel electrophoresis, which is used to separate pieces of DNA according to their size.
One common method for constructing a restriction map involves digesting the unknown DNA sample in three ways. Here, two portions of the DNA sample are individually digested with different restriction enzymes, and a third portion of the DNA sample is double-digested with both restriction enzymes at the same time. Next, each digestion sample is separated using gel electrophoresis, and the sizes of the DNA fragments are recorded. The total length of the fragments in each digestion will be equal. However, because the length of each individual DNA fragment depends upon the positions of its restriction sites, each restriction site can be mapped according to the lengths of the fragments. The information from the double-digestion is particularly useful for correctly mapping the sites. The final drawing of the DNA segment that shows the positions of the restriction sites is called a restriction map.
#GelElectrophoresis #RestrictionEnzyme #genetics #protein #agarose #usingAGelElectrophoresisMachine #DNAFingerprinting #howDoesAGelElectrophoresisMachineWork #biology #science #negativelyChargedDNA #restrictionEnzymes #guppies #basePairs #readingGelElectrophresis #DNAFragments #howDNAMovesThroughGelElectrophoresis #DNALadder #semilogGraph #purposeOfGelElectrophoresis #biotechnology #highSchool #stepsInElectrophoresis #NikolaysGeneticsLessons
1 view
44
26
10 months ago 00:00:32 1
[CHI2020] Norimaki Synthesizer: Taste Display Using Ion Electrophoresis in Five Gels
10 months ago 00:06:00 1
Sanger DNA Sequencing - Gel Electrophoresis Animation
11 months ago 00:07:55 4
Gel Electrophoresis
11 months ago 00:00:49 1
Ethidium bromide as mutagen
1 year ago 00:07:11 4
PCR and gel electrophoresis
1 year ago 00:04:18 1
Ethidium bromide | Liquid Nitrogen properties
1 year ago 00:04:09 1
Calculation of Agarose Gel Concentration
1 year ago 00:03:01 1
Trizol: Reagent for RNA, DNA, and Protein Isolation
2 years ago 00:04:35 1
Dyes for DNA staining
2 years ago 00:03:20 1
How to get rid of unspecific bands in Gel Electrophoresis
2 years ago 00:05:39 1
Why RNA Gel Electrophoresis result have small unexpected bands?
2 years ago 00:03:24 1
Why are the bands stuck in the wells during agarose gel electrophoresis?
2 years ago 00:07:23 1
Gel electrophoresis | pETDuet-1 vector
2 years ago 00:03:58 1
What caused such gel electrophoresis - explained
2 years ago 00:05:58 1
Bromophenol blue vs. Coomassie Brilliant Blue
2 years ago 00:08:02 1
Plasmid Gel Electrophoresis
2 years ago 00:03:51 1
Unusual “Spiky“ bands in Gel electrophoresis from restriction digest?
2 years ago 00:03:32 1
How to achieve good separation of leader bands in gel electrophoresis
2 years ago 00:04:58 1
How to count allele/polymorphism from the gel picture?
2 years ago 00:02:04 1
How to read, interpret and analyze DNA gel electrophoresis results?