How to fingerprint the bad guy

Slides:



Advertisements
Similar presentations
PACKET 11- DNA TECHNOLOGY. WHAT DO WE ALREADY KNOW ABOUT DNA?  DNA is __________ stranded  DNA is made up of four bases: ____, ____,_____, and _____.
Advertisements

Biotechniques. Gel electrophoresis Separates molecules according to size and charge. Different sized segments of DNA cut by restriction enzymes Segments.
Gel Electrophoresis of DNA Molecular Genetics Presentation by: Nana Sugma Mulyana Febrina Anggraini Ginting Faizal Dony Rifai Nor Aviva.
Biotech Lab #5 DNA Goes to the Races “Gel electrophoresis”
“Gel electrophoresis”. Gel electrophoresis is a procedure for separating a mixture of molecules through a stationary material (gel) in an electrical field.
Gel Electrophoresis & Gel Loading Practice. Gel Electrophoresis The process by which electricity is used to separate charged molecules (DNA fragments,
Lab 6: Molecular Biology Description – Gel electrophoresis cut DNA with restriction enzyme fragments separate on gel based on size.
Gel Electrophoresis.
& Gel Plasmid Electrophoresis Mapping.
Gel Electrophoresis. What is Gel Electrophoresis? Gel electrophoresis separates molecules on the basis of their charge and size. The charged macromolecules.
4.4 Using Gel Electrophoresis to Study Gene Molecules
Gel Electrophoresis Biotech I.
Gel Electrophoresis Lab
Electrophoresis Electrophoresis is the movement of molecules by an electric current .This is practically done in a matrix to limit migration and contain.
(RFLP Electrophoresis)
DNA Fingerprinting Simulation Step 1: Pour restriction enzymes into DNA.
Electrophoresis. Means literally to “carry with electricity.” Used to separate charged molecules such as DNA, RNA, & proteins. Larger (heavier) particles.
DNA is made of Nucleotides (p. 282). Nitrogen Bases.
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!
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Biotechnology Introduction Gel Electrophoresis. Method of analyzing DNA Allows a researcher to determine how alike or different two samples of DNA are.
Analysis of DNA Fragments with Gel Electrophoresis
Comparing DNA Aim: How can we compare organisms using gel electrophoresis? Do Now: Write two observations from your results of gel electrophoresis.
Restriction Enzyme Analysis of Lambda DNA DNA Fingerprinting of lambda DNA.
DNA Technology.
(RFLP Electrophoresis)
Gel Electrophoresis. Definition – COPY ME! Separation of DNA fragments according to size and charge Based on movement through a gel medium when an.
Desired Gene Restriction Enzymes Bacterial defense against viral DNA Bacterial defense against viral DNA Cut DNA at specific sequences Cut DNA at specific.
DNA fingerprinting is not taking someone’s fingerprint. It is cutting up a DNA strand and separating them by size.
Gel Electrophoresis.
PCR and Electrophoresis. Techniques of Recombinant DNA Technology Multiplying DNA in vitro: The Polymerase Chain Reaction (PCR) VIDEO CLIP ◦Large number.
Semester 2 Final Review Part 1 Genetics, Biotechnology, Protein Synthesis and Evolution.
Gel Electrophoresis of DNA. What is Gel Electrophoresis? Electro = flow of electricity, phoresis, from the Greek = to carry across A gel is a colloid,
What happens now that the DNA has been extracted?
Gel Electrophoresis By Erin Martin & Satya Moolani.
LAB 6 DNA FINGERPRINTING. BUILD the GEL FRAME Position comb and lock in place in side slots.
Biotechnology. Gel Electrophoresis A technique that separates macromolecules on the basis of their rate of movement through a gel under the influence.
Review Unit 1.3 Identity: Molecules and Cells. 1. What is the structure and the function of DNA? DNA Deoxyribonucleic acid – composed of nucleotides made.
Gel Electrophoresis. What is Gel Electrophoresis? Electrophoresis: Movement of charged particles through a solution (gel) under the influence of an electric.
Gel Electrophoresis.
Molecular Biology Part II: Gel Electrophoresis
Selective Breeding Limitations of selective breeding and mutations:
List general characteristics of all races
Gel Electrophoresis of DNA
Biotechnology.
Chapter 13.2 Manipulating DNA.
DNA Fingerprinting.
Gel Electrophoresis Method of separating molecules within an electric field based on the size and charge of DNA fragments.
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Biotech Lab #3 DNA Goes to the Races
Restriction Enzyme Analysis of Lambda DNA
DNA ELECTROPHORESIS OR DNA FINGERPRINTING.
Technology that uses electricity to separate molecules in a gel slab
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Electrophoresis / SDS-PAGE
Chapter 7 DNA Fingerprinting.
Unit 1.2 Review.
Restriction Enzymes The ability to cut and paste DNA predictably is due to the use of restriction enzymes. They were first identified in and isolated.
Creating a DNA Fingerprint by Gel Electrophoresis
Introduction to Gel Electrophoresis
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Unit 1.2 Review.
Gel Electrophoresis Ms. Cuthrell.
Gel Electrophoresis -samples with ligated DNA are loaded in a “gel” where they are run; an electric field is set up within the box -DNA has a slight charge,
DNA Agarose Gel Electrophoresis
ELECTROPHORESIS of serum proteins and dna
Micropipettes.
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
DNA Technology.
Gel Electrophoresis Gel Electrophoresis.
Presentation transcript:

How to fingerprint the bad guy DNA electrophoreisis How to fingerprint the bad guy

Electrophoresis This is a method for separating molecules that have a different : shape, size or electric charge.

It uses agarose gel. This is a polysaccharide made from sea weed. Because of the branches a solution makes a network where all the holes are the same size. The more concentrated the solution, the smaller the holes. A perfect molecular net.

How it works Make a gel with wells in it. Cut the DNA into small pieces with a restriction enzyme (More about this later) Cover the gel with an electrolyte solution. Load the wells with DNA This has to be done underwater with a micropipet

Running the gel Attach electrodes to a power supply and run an electrical current through the gel. If the molecules are charged + they will go to – terminal. If they are - they will migrate towards the positive terminal. + -

Smaller molecules will run faster than larger molecules be cause they fit through the net more easily. Streamlined molecules also travel faster.