Difference between revisions of "Part:BBa K4268000:Experience"

(Applications of BBa_K4268000)
 
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
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The part was received, resuspended, and cloned into the level 0 Golden Gate vector, PSB1C00. The ligation was then transformed into DH5&alpha; cells. After overnight growth, white colonies (indicative of a replacement of the RFP reporter cassette) were subjected to screening for the correct insert using colony PCR with the VF/VR primer pair.
how you used this part and how it worked out.
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===Applications of BBa_K4268000===
 
With the generosity of IDT, SUNY_Oneonta iGEM synthesized the Head-Tail Connector part. This part is RCF1000 compatible and contains SapI sites at either end of the sequence. The part was resuspended, restriction digested, and ligated into PSB1C00. The complex was then transformed into DH5&a cells and was left to grow overnight. After white colony growth was discovered in the transformed cells, five white colonies underwent a Colony PCR to determine if the desired insert was absorbed. 
 
  
Insert gel figure
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[[File: T-suny-oneonta-t7-head tail connector colony PCR figure.png|500px|thumb|center|Figure 1: Colony PCR of five colonies (clones) suspected of containing the Head-tail connector insert. The insert length is 1573bp and the predicted size of the PCR product when using VF/VR primers is 1878 bp.]]
Caption: Colony PCR of five colonies suspected of coating the insert and one colony containing an RFP.  
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At about 2000bp the gel indicates that all five colonies contain the insert. Thus
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The gel indicates that all five colonies are likely to contain the correct insert and thus, the Head-Tail Connector was successfully cloned into a Level 0 Golden Gate Assembly basic part.
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===Applications of BBa_K4268000===
  
 
===User Reviews===
 
===User Reviews===
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Latest revision as of 18:21, 8 October 2022


The part was received, resuspended, and cloned into the level 0 Golden Gate vector, PSB1C00. The ligation was then transformed into DH5α cells. After overnight growth, white colonies (indicative of a replacement of the RFP reporter cassette) were subjected to screening for the correct insert using colony PCR with the VF/VR primer pair.


Figure 1: Colony PCR of five colonies (clones) suspected of containing the Head-tail connector insert. The insert length is 1573bp and the predicted size of the PCR product when using VF/VR primers is 1878 bp.

The gel indicates that all five colonies are likely to contain the correct insert and thus, the Head-Tail Connector was successfully cloned into a Level 0 Golden Gate Assembly basic part.


Applications of BBa_K4268000

User Reviews

UNIQeb07073f4f064357-partinfo-00000000-QINU UNIQeb07073f4f064357-partinfo-00000001-QINU