Difference between revisions of "Part:BBa K3788001:Experience"
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<h2> PCR amplification of flag<i>Cry11Aa</i> gene : </h2> | <h2> PCR amplification of flag<i>Cry11Aa</i> gene : </h2> | ||
− | <p> The DNA sequence of flag<i>cry11Aa</i> was | + | <p> The DNA sequence of flag<i>cry11Aa</i> was amplified by PCR Q5 to generate fragment allowing a SLIC cloning. The expected size is <b>1956bp </b> and a 2000bp band is observed. Amplification of DNAs sequences with primers was validated.</p> |
https://2021.igem.org/wiki/images/a/a3/T--Aix-Marseille--DNA-SLIC-Amplification-xtoxtox.png | https://2021.igem.org/wiki/images/a/a3/T--Aix-Marseille--DNA-SLIC-Amplification-xtoxtox.png |
Latest revision as of 08:56, 21 October 2021
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Applications of BBa_K3788001
PCR amplification of flagCry11Aa gene :
The DNA sequence of flagcry11Aa was amplified by PCR Q5 to generate fragment allowing a SLIC cloning. The expected size is 1956bp and a 2000bp band is observed. Amplification of DNAs sequences with primers was validated.
Figure. Verification PCR amplification of DNAs sequence and these extensions for SLIC cloning. a. Control – (Absence of DNAs, no band expected); b, c, d, e. Amplification of 6hisp20_flagcry11Aa (expected 2500 bp), flagcry11Aa (expected 1847 bp), strepcyt1Aa (expected 775 bp) and 6hisp20 (expected 568 bp); L (SMART Ladder, its size is shown on the right side).
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