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Restriction Fragment Length Polymorphism (RFLP) Experiment Procedure For Student

나. Objective

Learn and master the basic principles and detection methods of Restriction Fragment Length Polymorphism (RFLP) genetic markers.

II. 원칙

The first generation of molecular genetic markers, RFLP, is based on mutations at the restriction enzyme cutting sites in the genomes of different varieties (individuals). These mutations can include base changes, insertions, deletions, or rearrangements between the enzyme-cutting sites, leading to variations in fragment sizes. These variations can be detected through PCR, restriction enzyme digestion, and agarose gel electrophoresis, allowing comparison of DNA level differences (즉., polymorphism) between different varieties (individuals). RFLP has been widely used in constructing genomic genetic maps, gene localization, biological evolution and classification, and genetic diversity studies.

III. Instruments, Materials, and Reagents

Instruments:

  • Electric constant temperature water bath
  • Agarose gel electrophoresis and detection system

Materials and Reagents:

  • Hind III restriction enzyme
  • 10×M Buffer
  • PCR product to be analyzed
  • DL2000 DNA Marker
  • 6×Loading Buffer
  • Sterile double-distilled water
  • 1.5% 아가로스 젤 (메모: Contains ethidium bromide (EB), which is carcinogenic; handle with gloves)
  • 0.5% TBE (electrophoresis buffer)

IV. 절차

  1. Hind III Restriction Enzyme Digestion

    • Reaction volume: 10 μL in a 0.2 mL Eppendorf tube
    • Add the following in order:
      • 10×M Buffer: 1 μL
      • ddH2O: 5.5 μL
      • Hind III: 0.5 μL
      • PCR product: 3 μL
    • Digest at 37℃ in a water bath for 2 시간. Use the entire digestion product for agarose gel detection.
  2. 아가로스 겔 전기영동

    • 준비하다 1.5% 아가로스 젤.
    • 혼합 10 μL of the digestion product with 1 μL of loading buffer.
    • Perform electrophoresis at a constant voltage of 180V.
    • DNA carries a negative charge, so it will migrate from the negative to the positive electrode during electrophoresis.
    • Stop electrophoresis when the DNA has migrated to 1/2 에게 2/3 of the gel’s length. Observe under a UV detector.

V. Assignment

Write the detailed procedure of this experiment and describe the results you observed (including drawings).

마틴 웡

저자는 박사 학위를 보유하고 있습니다.. 중국 농업대학교 생명과학 박사, 중국의 유명한 생물학 강사입니다., DTE의 창립자이기도 합니다.. 수상 경력으로 인정, 그는 학계에 적극적으로 참여하고 다음 세대의 학생들을 멘토링합니다., 학문적으로나 사회적으로 성공을 거두다.

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