Quiz #5 (9%) Biol710 11/7/12 name___________

Slides:



Advertisements
Similar presentations
You start with a biologically relevant protein from a pathogen (Bacterium, virus, parasite…)
Advertisements

DNA aSsEmBlY tEcHnIqUes Design and construct novel biological organisms programmed by genetic circuits using standardized biological parts called BioBricks.
Copyright © 2004 Pearson Education, Inc., publishing as Benjamin Cummings PowerPoint ® Lecture Slide Presentation prepared by Christine L. Case Microbiology.
The small sample of DNA serves as template for DNA polymerase Make complementary primers Add primers in more than 1000-fold excess Heat to make ssDNA,
Conversion of mRNA to cDNA by Reverse Transcription
Molecular Cloning: Construction of a recombinant DNA
Genomic DNA & cDNA Libraries
Concept 20.1: DNA cloning yields multiple copies of a gene or other DNA segment To work directly with specific genes, scientists prepare well-defined segments.
What causes LCA2 blindness?
-The methods section of the course covers chapters 21 and 22, not chapters 20 and 21 -Paper discussion on Tuesday - assignment due at the start of class.
Using mutants to clone genes Objectives 1. What is positional cloning? 2.What is insertional tagging? 3.How can one confirm that the gene cloned is the.
How do you identify and clone a gene of interest? Shotgun approach? Is there a better way?
BSL2016 / 2018 – Lecture 7 – cDNA libraries cDNA synthesis results in the generation of 1000’s of cDNA molecules. All these cDNA molecules are derived.
Chapter 4 Molecular Cloning Methods. Gene Cloning The Role of Restriction Endonuclease.
 Isolate a specific gene of interest  Insert into a plasmid  Transfer to bacteria  Grow bacteria to get many copies  Express the protein product 
Vectors Timothy G. Standish, Ph. D.. Vectors If a fragment of DNA is ligated into an appropriate vector, it can be inserted into cells which will then.
Remember the limitations? –You must know the sequence of the primer sites to use PCR –How do you go about sequencing regions of a genome about which you.
Recombinant DNA Technology Prof. Elena A. Carrasquillo Chapter 4 Molecular Biotechnology Lecture 4.
DNA Technology. 1.Isolation – of the DNA containing the required gene 2.Insertion – of the DNA into a vector 3.Transformation – Transfer of DNA into a.
Chapter 9 Biotechnology and Recombinant DNA Biotechnology: The use of microorganisms, cells, or cell components to make a product Foods, antibiotics, vitamins,
19.1 Techniques of Molecular Genetics Have Revolutionized Biology
Molecular Biology II Lecture 1 OrR. Restriction Endonuclease (sticky end)
中国免疫学信息网 SAGE 的原理及其应用 新乡医学院免疫学研究中心 王 辉.
RFLP ((Restriction Fragment Length Polymorphism)
Molecular Tools. Recombinant DNA Restriction enzymes Vectors Ligase and other enzymes.
Cloning DNA May 4.
Molecular Cloning.
Plasmids that contain l cos sites.
Biotechnology and Genetic Engineering PBIO 450/550 Gene libraries cDNA libraries Library screening.
Searching for Genes Important in Seed Development At1g19000 At1g74840 BY: Mike Douglas.
Arabidopsis Thaliana A Study of Genes and Embryo Development By Garen Polatoglu.
A Molecular Toolkit AP Biology Fall The Scissors: Restriction Enzymes  Bacteria possess restriction enzymes whose usual function is to cut apart.
Review for Exam 4 Jones and Bartlett Publishers © 2005.
710.LC GRADUATE MOLECULAR BIOLOGY 10/31/2011. Lecture 4 Competency Test.
Recombinant DNA & gene cloning Biology Donald Winslow 5 October 2010.
REVIEW OF MOLECULAR GENETICS DR. EDELBERG. Genes, DNA, & Chromosomes.
GENE CLONING TOOLS.
DNA cloning General strategies Choose DNA sources (gDNA/cDNA) Produce collection of DNA fragments Join them to appropriate vector Introduce rDNA to a host.
NAC Family Genes AT1G01720 AT1G77450
Cloning Club: Multiple proteins from one plasmid
Searching for the Genes that Control Seed Development
Are At1g08810 and At3g50060 Important to Arabidopsis Seed Development?
Lecture 8 A toolbox for mechanistic biologists (continued)
Cloning Club Introducing a deletion into a DNA sequence -Khushbu
Emily Eder HC70AL - Spring 2005
Biotechnology and Recombinant DNA
Quiz#3 LC710 9/29/10 name____________
Biotechnology and Recombinant DNA
Experimental Verification Department of Genetic Medicine
PCR Polymerase Chain Reaction
Name:_______________
Biotech Tools Review
Conversion of mRNA to cDNA by Reverse Transcription
Chapter 20 Biotechnology.
Quiz #7 (8%) Biol710 11/21/12 name___________
Biotechnology and Recombinant DNA
Quiz#7 LC710 10/18/10 name___________
710.LC GRADUATE MOLECULAR BIOLOGY 10/31/2011
From Gene to Protein.
710.LC GRADUATE MOLECULAR BIOLOGY 9/15/2010
Biotechnology and Genetic Engineering PBIO 4500/5500
(A) Schematic representation of kalata B1 showing the cyclic cystine knot, the amino acid sequence in single letter code, and the regions used for oligonucleotide.
Quiz#4 LC710 11/14/11 name___________
Quiz#4 LC710 10/04/10 name___________
Heat Shock Factor Protein Family of Transcription Factors
Genetically Modified Organisms
Hongli Lin, Xiangmei Chen, Jianzhong Wang, Zhiheng Yu 
He lab style.
Expression of multiple forms of MEL1 gene products.
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
Presentation transcript:

Quiz #5 (9%) Biol710 11/7/12 name___________ a) List the three ingredients for a functional plasmid used in cloning: _____ _____ _____ 3% b) What is the value of a multiple cloning site? (not needed for plasmid functionality!) _____________________________________________ 1% c) Draw an expression plasmid (all or none) whereby you can use it for testing enhancers: 2% Q2 You are planning to make a plasmid library to over express unknown proteins using eye cDNA. Your oligo dT primer for reverse transcription will have an EcoR1 site (GAATTC) on it, but now you are deciding between doing a Pac I (TTAATTAA) , a Bgl II (AGATCT) or a Bcl I (TGATCA) digest to open up the coding sequences for fusion into one of the three sets of vectors below. #1 ATG TTAATTAA GAATTC, ATGA TTAATTAA GAATTC, ATGAA TTAATTAA GAATTC #2 ATG AGATCT GAATTC, ATGA AGATCT GAATTC, ATGAA AGATCT GAATTC #3 ATG TGATCA GAATTC, ATGA TGATCA GAATTC, ATGAA TGATCA GAATTC Which set of vectors would you choose? (1%)_____ Give me two reasons why you wouldn’t choose the other two sets. (2%)__________ ___________