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each letter is a step:

R- Ribosomal trasfer

F- free DNA release

L- left sister chromosome divison

P- penile developement

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  1. Isolate DNA from the sample of interest.
  2. Digest the DNA with a restriction enzyme to cut it into fragments.
  3. Separate the fragments by size using gel electrophoresis.
  4. Transfer the fragments to a membrane and hybridize with a labeled probe to visualize the DNA fragments.
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Q: What are the steps in RFLP?
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What is the difference between a gene and RFLP?

A gene is a specific sequence of DNA that contains the instructions for making a particular protein or RNA molecule, while RFLP (restriction fragment length polymorphism) is a technique used to detect variations in DNA sequences by cutting DNA with restriction enzymes and separating the resulting fragments by size. In other words, a gene is a functional unit of DNA, while RFLP is a method to study genetic variation at the DNA level.


Is it possible for two people to have the exact same RFLP banding pattern?

It is highly unlikely for two people to have the exact same RFLP banding pattern due to the vast genetic variability among individuals. RFLP analysis is based on variations in DNA sequences, making it improbable for two unrelated individuals to have identical patterns.


What Is made during an RFLP analysis?

During an RFLP (Restriction Fragment Length Polymorphism) analysis, DNA is digested with restriction enzymes, separated by gel electrophoresis, and transferred to a membrane for hybridization with a probe. The resulting pattern of DNA fragments of varying lengths is visualized to identify variations in DNA sequences between individuals.


What is involved in a DNA test?

A DNA test involves collecting a sample, typically through a cheek swab or blood sample, and analyzing the DNA found in that sample. The DNA is then examined to look for specific genetic markers or variations that can provide information about an individual's ancestry, health, or relatedness to others. The results of the test are typically provided in a report that summarizes the findings.


Differences in DNA sequence on homologous chromosomes that can result in different patterns of restriction fragment lengths?

These differences are known as single nucleotide polymorphisms (SNPs) or insertions/deletions (indels), which can lead to variations in restriction enzyme recognition sites along the DNA sequence. This can result in different sized restriction fragments being produced when the DNA is cut with restriction enzymes, yielding distinct patterns on a gel during a restriction fragment length polymorphism (RFLP) analysis.