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Analyzing Gels

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What are the cut standards (base pair size) of Lambda DNA with HIND III? ... Lambda HIND III. Lambda. 48,000 bp. On the gel DNA gets hung up at 25,000 bp ... – PowerPoint PPT presentation

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Title: Analyzing Gels


1
Analyzing Gels
  • Biotech 1

2
Questions to answer before
  • What is a plasmid?
  • How many chromosomes does Yeast have?
  • What are the cut standards (base pair size) of
    Lambda DNA with HIND III?

3
What type of DNA did we use?
  • Salmon Sperm
  • Animal
  • E.Coli
  • Bacteria
  • Yeast
  • Eukaryotic
  • Lambda
  • Virus
  • Lambda HIND III
  • Virus DNA cut with an enzyme called HIND III
  • pAMP
  • Plasmid that makes an enzyme to break down
    ampicilin
  • pUC19
  • Plasmid

4
What are plasmids?
  • Small pieces of DNA
  • Origin of Replication
  • Antibiotic Resistance
  • Promoter
  • Gene of Interest

5
What does a band (line) mean on a gel?
  • Each band is a certain amount of base pairs (bp).
  • With large number of base pairs at the top
  • Smaller number base pairs at bottom

6
How do we tell how big a piece of DNA is?
  • Standards - Which one did we use?
  • Lambda cut with HIND III - What are the sizes?

7
Lambda
  • What is your estimate of Lambda?
  • Why is Lambda one line?

On the gel DNA gets hung up at 25,000 bp
48,000 bp
8
Salmon Sperm
  • What do you think the size of SS is?
  • Why do you think it smears?

9
E.coli
  • What do you estimate the size of E.coli is?
  • Why do you think it is different from Salmon
    Sperm?
  • Why is one E.coli lighter than the other?

10
Yeast
  • What is the size of Yeast?

11
pUC19
2686 bp
12
pAMP
  • Which band on pAMP do we want to read?
  • What do you think the size of pAMP is?

13
Mistakes
  • Look at the edges?
  • What do you notice about the DNA?

HIGH VOLTAGE
14
Mistakes
  • Where is the DNA?

Poor Pipetting
15
Mistakes
  • What do you notice about the Salmon Sperm?

High concentration of DNA. Spills into other
wells.
16
Mistakes
  • What are some things you notice?

Agarose not fully melted, due to wavy lines.
17
Mistakes
  • Why is this incorrect?

18
Reflection
  • Label your DNA printout and analyze the results.

19
References
  • http//www.brunel.ac.uk/depts/bio/project/genome/m
    oltec/vectors/gifs/puc19.gif
  • http//www.mun.ca/biochem/courses/4103/figures/Sny
    der-Champness/F4-1.jpg
  • http//occawlonline.pearsoned.com/bookbind/pubbook
    s/bc_mcampbell_genomics_1/medialib/method/inducepr
    omoter.gif
  • http//www.dnalc.org/images/pamp.jpg
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