Difference between revisions of "Part:BBa K2669002:Experience"
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<p>Stability assay through liquid experiment was performed with all three plasmids in the IDT supplied backbone. 1 mL of LB with ampicillin (25 ug/ml) was inoculated with one single colony in eppendorf tubes in 10 replicates for each part. In order to allow 10 generations of growth, a 1:1000 dilution was made and incubated for 24 h. The colour comparison was done through visualization of centrifuged cultures and by analyzing the color intensity we could deduce the stability of the protein. </p> | <p>Stability assay through liquid experiment was performed with all three plasmids in the IDT supplied backbone. 1 mL of LB with ampicillin (25 ug/ml) was inoculated with one single colony in eppendorf tubes in 10 replicates for each part. In order to allow 10 generations of growth, a 1:1000 dilution was made and incubated for 24 h. The colour comparison was done through visualization of centrifuged cultures and by analyzing the color intensity we could deduce the stability of the protein. </p> | ||
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<p> Already after 10 generations it was clearly visible that more IDT optimized colonies had the strongest color compared to the original amilCP colonies. This indicates that the stability of the IDT optimized AmiLCP is greater than for the original AmilCP sequence. | <p> Already after 10 generations it was clearly visible that more IDT optimized colonies had the strongest color compared to the original amilCP colonies. This indicates that the stability of the IDT optimized AmiLCP is greater than for the original AmilCP sequence. | ||
Revision as of 13:28, 6 October 2018
Contents
TRANSFORMATION RESULTS
Figure 1:Transformation plate of the IDT optimized AmilCP sequence. The circled colonies represent the colonies used in the stability assay.
Figure 2:Transformation plate of the original AmilCP sequence. The circled colonies represent the colonies used in the stability assay.
STABILITY ASSAY
Stability assay through liquid experiment was performed with all three plasmids in the IDT supplied backbone. 1 mL of LB with ampicillin (25 ug/ml) was inoculated with one single colony in eppendorf tubes in 10 replicates for each part. In order to allow 10 generations of growth, a 1:1000 dilution was made and incubated for 24 h. The colour comparison was done through visualization of centrifuged cultures and by analyzing the color intensity we could deduce the stability of the protein.
Figure 3: The result after 10 generations. The upper row represent 10 different colonies of the IDT optimized sequence of AmiLCP. The lower row represents the original AmilCP sequence.
INTERPRETATION
Already after 10 generations it was clearly visible that more IDT optimized colonies had the strongest color compared to the original amilCP colonies. This indicates that the stability of the IDT optimized AmiLCP is greater than for the original AmilCP sequence.
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