Different DNA Extraction Methods The organic method generally yields the highest quantity and quality DNA. The main disadvantages are that it is tedious.

Slides:



Advertisements
Similar presentations
Amanda Barrera Biology Honors Period 1
Advertisements

PCR, Gel Electrophoresis, and Southern Blotting
DNA Analysis Techniques
Laser Microdissection
Biotech Lab #5 DNA Goes to the Races “Gel electrophoresis”
GEL ELECTROPHORESIS Lab.5. Gel electrophoresis is a method used to separate nanoparticles by charge or size. It is used to: 1. separate a mixed population.
By: Jennifer Oxford, Jacob Carter, Elemuel Coleman.
Restriction Digestion of Arabidopsis thaliana Genomic DNA
RESTRICTION FRAGMENT LENGTH POLYMORPHISM RFLP. 1. Extraction The first step in DNA typing is extraction of the DNA from the sample, be it blood, saliva,
Gel Electrophoresis.
Agarose Gel Electrophoresis.
Fundamentals of Forensic DNA Typing
Protein Electrophoresis BIT 230. Electrophoresis Separate proteins based on Size (Molecular Weight - MW) SDS PAGE Isoelectric Point Isoelectric focusing.
Y.Martinez.
Lecture 19, Chapter 11 Analysis of transgenic plants part II Neal Stewart.
DNA Fingerprinting & Forensic Analysis. How is DNA Typing Performed? Only one-tenth of 1% of DNA differs in each person; this variation can create.
Electrophoresis Electrophoresis is the movement of molecules by an electric current .This is practically done in a matrix to limit migration and contain.
A tool for separating specific biomolecules from a mixture (A key step in most biotechnology applications) Electrophoresis.
Gel Electrophoresis of DNA
(RFLP Electrophoresis)
DNA Fingerprinting. We share 99.9% of our DNA with each other. That means the 0.1% of our DNA makes us unique. But that is still is over 3,000,000 differences!
Lab.8 8RBs0Ghg_48
Gel Electrophoresis and Probes (Southern Blotting) Group A,
Western Blotting.
Visualizing DNA. What is it?  Gel electrophoresis is one of the techniques scientists use to look at the DNA they have.  This technique separates DNA.
RFLP Analysis Restriction Fragment Length Polymorphism 1.Extract/Isolate DNA from the cell restriction enzymes 2.Cut DNA into smaller fragments using restriction.
PCR is DNA replication in a test tube Ex. 25: PCR Based Testing for Water Contaminants Day 2.
(RFLP Electrophoresis)
Gel electrophoresis is a method for separation and analysis of macromolecules(DNA, RNA and proteins) and their fragments, based on their size and charge.
PCR and Electrophoresis. Techniques of Recombinant DNA Technology Multiplying DNA in vitro: The Polymerase Chain Reaction (PCR) VIDEO CLIP ◦Large number.
DNA extraction.
Science Fact of the Day: Hummingbirds can't walk..
Manipulating DNA. Scientists use their knowledge of the structure of DNA and its chemical properties to study and change DNA molecules Different techniques.
Advantages of STR Analysis
Lecturer: David. * Reverse transcription PCR * Used to detect RNA levels * RNA is converted to cDNA by reverse transcriptase * Then it is amplified.
Electrophoresis 7 th Grade,. Learning Objectives Understanding how electrophoresis facilitates the separation of molecules Be familiar with the types.
DNA Science. Restriction Digest Restriction Digestion is the process of cutting DNA molecules into smaller pieces with special enzymes called Restriction.
Semester 2 Final Review Part 1 Genetics, Biotechnology, Protein Synthesis and Evolution.
DNA Technology Ch. 20. The Human Genome The human genome has over 3 billion base pairs 97% does not code for proteins Called “Junk DNA” or “Noncoding.
MOLECULAR GENETICS TECHNIQUES. Molecular Genetics Technologies i.Polymerase chain reaction ii.DNA/Genomic sequencing iii.Gel electrophoresis iv.Restriction.
Page Gel Electrophoresis gel electrophoresis – moving DNA through a gel medium using an electric current Why can we move DNA with electricity?
Applications & Analysis DNA Gel Electrophoresis 1.
What happens now that the DNA has been extracted?
Gel Electrophoresis By Erin Martin & Satya Moolani.
CLONING DNA PART II. REVIEW: CHALLENGE REMEMBER THIS?
Gel Electrophoresis gel electrophoresis – moving DNA through a gel medium using an electric current Why can we move DNA with electricity? DNA has a negative.
Biotechnology. Gel Electrophoresis A technique that separates macromolecules on the basis of their rate of movement through a gel under the influence.
Gel Electrophoresis + restriction enzymes Lecturer: Bahiya Osrah.
DNA Forensics 352 – O’Dette. Why DNA? DNA is individual evidence DNA links or eliminates a suspect to a crime DNA identifies a victim even if no body.
DNA Fingerprinting Review. Why DNA? DNA is individual evidence DNA links or eliminates a suspect to a crime DNA identifies a victim even if no body is.
JS 113: Introduction to DNA Typing I.Pre class activities a.Quiz b.Schedule update c.Announcements and Assignments II. Learning Objectives a.Understand.
Gel Electrophoresis Technique for separating DNA molecules based on size Load DNA mixture into gel containing pores of varying sizes Subject DNA to electric.
DNA fingerprinting Synonyms DNA Profiling DNA typing DNA testing.
Understanding Gel Electrophoresis
DNA Analysis Target 3-2.
PCR and RLFP’s.
DNA Extraction and Analysis: and 1.2.3
DNA Technology.
Gel Electrophoresis Method of separating molecules within an electric field based on the size and charge of DNA fragments.
Slot blot hybridization
DNA Technology.
Presented by: Ihsan Ullah M Imran Sharif
Visualizing DNA Gel Electrophoresis.
Creating a DNA Fingerprint by Gel Electrophoresis
DNA Fingerprinting and Forensic Analysis
History of DNA Fingerprinting
Laser Microdissection
Forensic Characterization of Bloodstains cont’d
How to fingerprint the bad guy
DNA Technology.
Presentation transcript:

Different DNA Extraction Methods The organic method generally yields the highest quantity and quality DNA. The main disadvantages are that it is tedious with lots of steps and utilizes corrosive chemicals. The Chelex method is used when the sample contains very few cells and the reduced number of handling steps is the primary advantage. The main disadvantage is that it is yields crude DNA that is not as pure FTA paper is used to collect reference samples. It can be stored at room temperature, requires minimal handling and no quantification is required.

Differential Extraction Method For Sexual Assault Evidence Isolation of DNA from mixtures of cells in sexual assault evidence Based on differences in cell membranes –Spermatozoa membranes have special cross links (sulphur- sulphur bonds) –These membranes are quite resistant to opening. –Vaginal epithelial cells do not contain these membranes and are more easily broken open Sperm and v cell mixture Lysis- open v cell  extract Female DNA Male DNA Female cell Spermatozoa Lysis- open sperm  extract Male DNA

Quantification of DNA Following extraction, the next step is to determine the quantity of the DNA DNA typing methods RFLP and PCR require different amounts and different quality of DNA. RFLP typically required 50ng. PCR typically requires less than 0.5ng to 1 ng: 100 times less!

Quantification of DNA using Gel Electrophoresis Total DNA can be quantified by running the samples in a gel. Typically, gels are made up of agarose (a carbohydrate from seaweed). Known DNA quantities are included Samples are then subject to an electric current and is called electrophoresis. DNA is negatively charged and will migrate toward the positive electrode… Comparisons of the results are done visually or with computer software to determine the amount of DNA in the unknown sample. (-) (+) wells Intact DNA Degraded DNA L K K – u u u Direction of DNA fragment movement Smaller fragments move faster and are found Near the bottom of the gel

Slot Blot quantification : DNA-DNA Hybridization DNA is where it’s AT DNA samples may contain non human DNA In order to quantify the amount of human DNA in a sample, a human specific test is required One such test is DNA-DNA hybridization using a human specific probe: D17Z1