Measurement

Part:BBa_K1510820

Designed by: Kao Jung Chang   Group: iGEM14_NYMU-Taipei   (2014-10-07)

RFP indicated INPNC performance evaluation

We anneal a RFP at the end of our INPNC display gene.We adopted a new method that measuring fluorescence light and O.D value of our modified e-coli to test the efficiency of INPNC expression. We successfully derived INPNC expression quantity and expression curve though time. And successfully proved that our targeted gene CSP16 is on the surface of our modified e-coli.

First test After centrifugation, the supernatant is clear; we could indicate that CSP16 is not secreted out of cell. Also, indicated from the red fluorescence of the pellet, we could say that INPNC protein display CSP16 and RFP on the surface. NYMU Cohesion picture.jpg


Second test At the beginning, the population of E. coli is small as well as OD, so initial figure (Fluorescence /OD) is large. As time proceeds, Fluorescence /OD level increases dramatically, indicating that the INPNC protein is being greatly expressed. The OD level reaches a plateau at the end.NYMU Cohesion picture2.jpg


Fluorescence level /OD level indicates the display function of INPNC through growth time.NYMU Cohesion picture3.jpg

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1036
    Illegal AgeI site found at 2220
    Illegal AgeI site found at 2332
  • 1000
    COMPATIBLE WITH RFC[1000]


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