Week 6 Team has split into Dry Lab and Wet Lab Dry Lab: Wet Lab:

Slides:



Advertisements
Similar presentations
5 Stages involved in GE Isolation Cutting Ligation and Insertion
Advertisements

You start with a biologically relevant protein from a pathogen (Bacterium, virus, parasite…)
Ch. 2A: How Do You Begin to Clone a Gene?. Learning goals Describe the characteristics of plasmids Explain how plasmids are used in cloning a gene Describe.
Goal: To persuade a bacterium to produce a variety of small peptides and secrete them into the medium.
Chapter 4: recombinant DNA
Gel Scramble Lecture 1 William Grisham, Ph.D. Copyright 2014.
Molecular Cloning: Construction of a recombinant DNA
Definition The terms recombinant DNA technology, DNA cloning, molecular cloning, or gene cloning all refer to the same process: the transfer of a DNA.
Bacteria Transformation
Introduction recombinant expression of protein disulfide isomerase (PDI) using the model plant Arabidopsis thaliana Eun Ju Cho ABE workshop 2007.
Encapsulation for Drug Delivery
Welcome! to the “Modern Lab” section
Yesterday: Genetic Disorders and Gene Therapy
Bacillus subtilis expression/secretion systems
Select transformants on LB plates containing 100 μg/ml ampicillin  Successful colonies K562: 27 colonies Hela: 11 colonies IM9: 25 colonies Lab Meeting.
AP Biology Biotechnology Part 2 Genetics of Bacteria.
Lab 21 Goals and Objectives: Exercise 59: Bacteriological Examination of Water Confirmed Test: check EMB plate for coliforms EDVOKIT#300: Blue/White Cloning.
Chapter 9 Biotechnology and Recombinant DNA Biotechnology: The use of microorganisms, cells, or cell components to make a product Foods, antibiotics, vitamins,
Lecture 7 Manipulation of foreign gene and secretion of foreign protein.
Lecture22 &23 DNA microinjection. DNA MICROINJECTION direct microinjection of a chosen gene construct direct microinjection of a chosen gene construct.
RNA and Protein Synthesis. How does DNA determine our traits?
RECOMBINANT DNA TECHNOLOGY PART 2 Quiz Essay 2 Topics Molecular Topics: 35 points Emphasis: data interpretation, critical thinking with a short answer.
Bacterial genetics by E. Börje Lindström This learning object has been funded by the European Commissions FP6 BioMinE project.
Microbial Genetics - DNA Transfer l Review of Information Transfer in Cell l Recombination l Transfer of DNA &Genetic Recombination in Bacteria –Conjugation.
Genetic Engineering Genetic engineering involves the manipulation of organism genes. The central tool is the recombinant DNA technique. - to isolate a.
Trends in Biotechnology Constructing and Screening a DNA Library.
Cloning DNA, Plasmids and Transformations By: Stephen Sullivan and Julie Ethier.
Ch. 2A: How Do You Begin to Clone a Gene?. Learning goals Describe the characteristics of plasmids Explain how plasmids are used in cloning a gene Describe.
Encapsulation for Drug Delivery Encapsulation for Drug Delivery 31 st July iGEM Team 2009 Charles Dave Dineka James Kun Nuri Royah Tianyi.
Microbial Genetics.
Gateway Cloning 13 November 2013.
- making changes to the DNA code of a living organism.
Sadia Sayed. The expression of the cloned gene in a selected host organism. It does not necessarily ensure that it will be successfully expressed. A high.
Topics to be covers Basic features present on plasmids
E.Coli AS MODERN VECTOR.
V Cell Transformation Recombinant DNA Host Cell DNA Target gene
RNA and protein synthesis
YAC and BAC cloning systems
Relative luciferase activity Relative luciferase activity
Biotechnology and Recombinant DNA
Recombinant DNA (rDNA) technology
Control of Gene Expression
Biotechnology and Recombinant DNA
Genetic Engineering Chapter 11 Section 1.
Introduction to Yeast Plasmids
YAC and BAC cloning systems
13-3 Cell Transformation Interactive pgs. 329.
Figure 7.1 Polymerase chain reaction (PCR).
Dr T-J’s Minilecture Chapter 12.
EDVOKIT#300: Blue/White Cloning of a DNA Fragment
Hash In-Class Quiz.
Biotechnology Part 2 Genetics of Bacteria
Biotechnology and Recombinant DNA
Example construct we would want to construct in B.subtilis
Copyright Pearson Prentice Hall
The Goal Put together the parts we have now (and some parts we’re still missing) to make: LacI, TetR, and cI Lambda coding regions w/ hi/low constitutive.
“The natural genetic engineer”
Gel Retardation.
Standardized and Scalable DNA Assembly
Genetic Engineering Subtitle.
BioBricks.
RNA and protein synthesis
Copyright Pearson Prentice Hall
The Baccelerator: Back on track…
Biotechnology Part 2 Genetics of Bacteria
Cell Transformation.
Producing DNA fragments eg for manufacturing insulin
Unit 4 - The Natural Environment and Species Survival
Biotechnology Practice Test
E.Coli AS MODERN VECTOR.
Presentation transcript:

Week 6 Team has split into Dry Lab and Wet Lab Dry Lab: Wet Lab: Erika, - James, Prudence, -Chris, Clinton, -Tom, Yanis, -Krupa,

Wet Lab Two key tasks: DNA synthesis Protocols and Reagents

DNA Synthesis Genes Terminators Promoter and RBS

Promoters RBS Promoter and RBS Inducible Constitutive 1.p43 Sigma B 1.Phyper-spank 2.pXyl Constitutive 1.p43 2.pVeg Sigma B 1.pctc 2.pgsiB RBS =12 combinations 1.gsiB 2.spoVG

Genes Genes Signal Peptide Biomaterials Registry Light+Motility 1.YtvA 2.EspE Signal Peptide 1.SacB 2.LipA Biomaterials 1.Elastin 2.EAK 16 Registry 1.Antibiotics 2.GFPmut3b =4 Combinations

Insertion Sequence Terminators Terminators Registry Insertion Sequence 1.Double Terminator Insertion Sequence 1.PyrD 2.AmyE

Protocols Cloning, Culturing, Transformation, Testing,

Cloning

Culturing and Transformation This week we are planning to test culturing and transformation using integration vector. If successful will linearise vector and test for linear integration

Have defined testing Constructs. This week need to work out testing protocols, Microscope training on Thursday!