1. PLATE NORMAL L WITHOUT PLASIMID +DMA -DNA --DAMP +TH-REASH +AMP NORMAL ALUWTH WITHOUT PLASIMID NO AFTIBOTIC RESITE INDUSIN RESISTANCE WIT PROSMID WITHOUT PLASMID AMP +AMP 5. -DNA +-AMP +AMP 4. PLATE +AMP. +IAMP -DNA -DNA/+AMP +DNA/+AMP +DNA/+AMP/+IPTG • No plasmid • No plasmid • Plasmid Plasmid No ampicillin • Ampicillin • Ampicillin • Ampicillin • No IPTG • No IPTG • No IPTG • IPTG
1. PLATE NORMAL L WITHOUT PLASIMID +DMA -DNA --DAMP +TH-REASH +AMP NORMAL ALUWTH WITHOUT PLASIMID NO AFTIBOTIC RESITE INDUSIN RESISTANCE WIT PROSMID WITHOUT PLASMID AMP +AMP 5. -DNA +-AMP +AMP 4. PLATE +AMP. +IAMP -DNA -DNA/+AMP +DNA/+AMP +DNA/+AMP/+IPTG • No plasmid • No plasmid • Plasmid Plasmid No ampicillin • Ampicillin • Ampicillin • Ampicillin • No IPTG • No IPTG • No IPTG • IPTG
Biology: The Unity and Diversity of Life (MindTap Course List)
14th Edition
ISBN:9781305073951
Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Chapter20: Viruses, Bacteria, And Archaea
Section: Chapter Questions
Problem 6SQ
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Question
a) Calculating Transformation Efficiency
For the +DNA/+Amp/+IPTG plate, record the following:
Number of transformants (colonies): _________________
Nanograms of plasmid DNA added: 50 ng
Final recovery volume: 0.50 mL
Volume plated: 0.25 mL
Transformation efficiency equation:
Transformation efficiency = Number of transformants / µg of DNA x Final volume at recovery (mL)/ volume plated (mL)
b) Using the equation above, calculate the transformation efficiency.
c) Describe the success of the transformation efficiency of this demo based on the calculation you did above?
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