サインイン

Agarose gel electrophoresis is a laboratory technique commonly used to separate DNA fragments by size. However, it can also be used to isolate and purify DNA fragments using a gel extraction protocol.

Gel extraction follows five major steps: running gel electrophoresis to separate fragments, isolating the individual bands, extracting DNA from those bands, and removing the dye and salts from the extracted mixture to obtain pure DNA.

In cloning experiments, both the insert and vector DNA fragments are obtained after digestion with restriction endonucleases. These DNA fragments of varying sizes are mixed with contaminants, such as enzymes, salts, etc., that can inhibit the ligation reaction that follows. Gel extraction is therefore used to obtain pure DNA fragments before ligation.

To set up a gel for extraction, a lower percent (0.7-0.8%) agarose solution is used to ensure efficient migration of the DNA bands. In addition, a wide-combed gel cast is used to obtain thick DNA bands that are easy to isolate. Then, gel electrophoresis is performed at a lower voltage to prevent heating of the gel and damage to the DNA.

Once gel electrophoresis is complete, the ethidium bromide-stained DNA is identified by exposing the gel to long-wavelength UV for a short time. Short exposure to UV radiation prevents damage to DNA. This is followed by cutting out the desired band using a clean razor blade.

The isolated gel slice containing the DNA fragment of interest is then processed through one of the commercially available gel extraction kits. All of these kits follow the same basic principle. First, the agarose gel is dissolved by a buffer solution containing salts, such as sodium iodide. Next, DNA is bound to a column containing an anionic resin and washed a few times with a dilute alcoholic solution to remove impurities. The column is then dried by spinning in a centrifuge. The pure DNA can now be eluted with buffer or deionized water.

タグ

DNA Agarose Gel ElectrophoresisGel ExtractionDNA FragmentsSize SeparationPurificationCloning ExperimentsVector DNAInsert DNARestriction EndonucleasesContaminantsLigation ReactionAgarose SolutionMigration Of DNA BandsWide combed Gel CastLower Voltage ElectrophoresisEthidium Bromide StainingUV ExposureGel Slice Isolation

章から 15:

article

Now Playing

15.3 : DNA Agarose Gel Electrophoresis

DNAとRNAを研究する

91.5K 閲覧数

article

15.1 : 組換えDNA

DNAとRNAを研究する

16.4K 閲覧数

article

15.2 : DNA単離

DNAとRNAを研究する

36.8K 閲覧数

article

15.4 : DNAプローブのラベリング

DNAとRNAを研究する

8.0K 閲覧数

article

15.5 : サザンブロット

DNAとRNAを研究する

17.5K 閲覧数

article

15.6 : DNAマイクロアレイ

DNAとRNAを研究する

16.9K 閲覧数

article

15.7 : 相補的DNA

DNAとRNAを研究する

5.5K 閲覧数

article

15.8 : FISH - 蛍光 In-situ ハイブリダイゼーション

DNAとRNAを研究する

18.9K 閲覧数

article

15.9 : PCR - ポリメラーゼ連鎖反応

DNAとRNAを研究する

80.4K 閲覧数

article

15.10 : リアルタイムRT-PCR

DNAとRNAを研究する

56.0K 閲覧数

article

15.11 : RACE - cDNA末端の迅速な増幅

DNAとRNAを研究する

6.2K 閲覧数

article

15.12 : サンガーシーケンシング

DNAとRNAを研究する

750.1K 閲覧数

article

15.13 : 次世代シーケンシング

DNAとRNAを研究する

85.3K 閲覧数

article

15.14 : RNA-seq(英語)

DNAとRNAを研究する

9.5K 閲覧数

article

15.15 : ゲノムアノテーションとアセンブリ

DNAとRNAを研究する

18.6K 閲覧数

See More

JoVE Logo

個人情報保護方針

利用規約

一般データ保護規則

研究

教育

JoVEについて

Copyright © 2023 MyJoVE Corporation. All rights reserved