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Related Concept Videos

Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
Restriction Enzymes01:11

Restriction Enzymes

Restriction enzymes are bacterial enzymes used to cut DNA in a sequence-specific manner. To cleave DNA, they bind to specific palindromic sequences called restriction sites. Such palindromic DNA sequences or inverted repeats are commonly found in regions of functional significance, such as the origin of replication, gene operator sites, and regions containing transcription termination signals.
The host bacteria protect their own genomic DNA from these enzymes by methylating these sites. Some...
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Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
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Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...

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Related Experiment Video

Updated: Jul 5, 2026

A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
08:22

A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene

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Restriction fragment length polymorphism analysis.

J Jarcho1

  • 1Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Current Protocols in Human Genetics
|April 23, 2008
PubMed
Summary

Restriction Fragment Length Polymorphism (RFLP) analysis uses DNA digestion to detect genetic variations. This method traces the inheritance of specific DNA fragments across generations within families.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biotechnology

Background:

  • Genetic variations can be identified using DNA analysis techniques.
  • Restriction Fragment Length Polymorphism (RFLP) is a method for detecting these variations.

Purpose of the Study:

  • To describe the methodology of Restriction Fragment Length Polymorphism (RFLP) analysis.
  • To explain how RFLP can be used to study the inheritance of DNA sequence polymorphisms within families.

Main Methods:

  • Genomic DNA is digested with specific restriction enzymes.
  • DNA fragments are separated by size using agarose gel electrophoresis.
  • DNA is transferred to a membrane (Southern blot) for hybridization with a labeled probe.
  • Washing and X-ray film exposure identify specific DNA fragments.

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Related Experiment Videos

Last Updated: Jul 5, 2026

A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
08:22

A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene

Published on: September 16, 2019

Modified Terminal Restriction Fragment Analysis for Quantifying Telomere Length Using In-gel Hybridization
11:29

Modified Terminal Restriction Fragment Analysis for Quantifying Telomere Length Using In-gel Hybridization

Published on: July 10, 2017

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

Main Results:

  • Identified DNA fragment sizes vary among individuals.
  • These variations can be traced through family generations, demonstrating inheritance patterns.

Conclusions:

  • RFLP analysis is a valuable tool for identifying and tracing DNA sequence polymorphisms.
  • The technique facilitates the study of genetic inheritance patterns in families.