Revision as of 05:53, 22 September 2015

Pcons+B0034+Lpp-OmpA-N+scFv(Anti-HER2)+B0030+GFP+J61048

Introduction:

Fig.1 Pcons+RBS+Lpp-OmpA-N+Anti-HER2+RBS+GFP+Ter

Transformation of single plasmid

To prove that our scFv can actually bind on to the antigen on cancer cells, we connected each scFv with a different fluorescence protein. Therefore, we could use fluorescence microscope to clearly observe if the E. coli has produced scFv proteins. Currently,we built three different scFv connected with their respectively fluorescence protein, which are Anti-VEGF+GFP, Anti-EGFR+RFP, Anti-HER2+BFP. When applied on cell staining, we can identify the antigen distribution on cancer cells by observing the fluorescence. Furthermore, if we use the three scFv simultaneously, we can also detect multiple markers. We also built combinations each scFv connected with green fluorescence protein.

Fig.2 Transformation of single plasmid

Experiment

1.Cloning

Fig.3 The PCR result of the Pcons+B0034+Lpp-OmpA-N+scFv(Anti-HER2)+B0030+GFP+J61048. The DNA sequence length is around 1900~2100 bp, so the PCR products should appear at 2100~2300 bp.

After assemble the DNA sequences from the basic parts, we recombined each Pcons+B0034+Lpp-OmpA-N+scFv(Anti-HER2)+B0030+GFP+J61048 gene to PSB1C3 backbones and conducted a PCR experiment to check the size of each of the parts. The DNA sequence length of the these parts are around 1900~2100 bp. In this PCR experiment, the PCR products size should be near at 2100~2300 bp. The Fig.3 showed the correct size of this part, and proved that we successful ligated the sequence onto an ideal backbone.

Fig.4 Pcons+B0034+Lpp-OmpA-N+scFv(anti-HER2)+B0030+GFP+J61048

Sequence and Features