Coding

Part:BBa_K4268001:Experience

Designed by: J. Aubrey, J. Alvarenga, L. Buchanan, J. Reyes, D. Yashinski   Group: iGEM22_SUNY_Oneonta   (2022-07-26)
Revision as of 16:22, 8 October 2022 by Jazmine124 (Talk | contribs)


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 coating the insert Capsid Assembly Protein insert. The insert length is 768bp and the predicted size of the PCR product when using VF/VR primers is 1073 bp.

The gel indicates that colonies 1 and 2 are likely to contain the correct insert and thus, the Capsid Assembly Protein was successfully cloned into a Level 0 Golden Gate Assembly basic part.


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UNIQ4e09693d23c972c7-partinfo-00000000-QINU UNIQ4e09693d23c972c7-partinfo-00000001-QINU