Difference between revisions of "Part:BBa K2656013"
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Part BBa_K2656013 is the super folder Green Fluorescent Protein coding secuence [https://parts.igem.org/Part:BBa_I746916 BBa_I746916] compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/GB3 Golden Braid 3.0] assemply methods. It can be combined with other compatible part from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the [http://2018.igem.org/Team:Valencia_UPV/Protocols Golden Gate assembly protocol]. | Part BBa_K2656013 is the super folder Green Fluorescent Protein coding secuence [https://parts.igem.org/Part:BBa_I746916 BBa_I746916] compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/GB3 Golden Braid 3.0] assemply methods. It can be combined with other compatible part from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the [http://2018.igem.org/Team:Valencia_UPV/Protocols Golden Gate assembly protocol]. | ||
− | The charcterization of this protein (and by extension of all the other part that codify for the sfGFP) has been performed with our transcriptional unit [https://parts.igem.org/Part: | + | The charcterization of this protein (and by extension of all the other part that codify for the sfGFP) has been performed with our transcriptional unit [https://parts.igem.org/Part:BBa_K2656101 BBa_K2656101]. |
This transcriptional unit [https://parts.igem.org/Part:BBa_K2656100 BBa_K2656100] was assembled in a Golden Braid alpha1 plasmid'''(REF)''' including the following parts: | This transcriptional unit [https://parts.igem.org/Part:BBa_K2656100 BBa_K2656100] was assembled in a Golden Braid alpha1 plasmid'''(REF)''' including the following parts: | ||
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Revision as of 10:51, 29 September 2018
sfGFP Coding Sequence
Part BBa_K2656013 is the super folder Green Fluorescent Protein coding secuence BBa_I746916 compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/GB3 Golden Braid 3.0] assemply methods. It can be combined with other compatible part from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the [http://2018.igem.org/Team:Valencia_UPV/Protocols Golden Gate assembly protocol].
The charcterization of this protein (and by extension of all the other part that codify for the sfGFP) has been performed with our transcriptional unit BBa_K2656101. This transcriptional unit BBa_K2656100 was assembled in a Golden Braid alpha1 plasmid(REF) including the following parts:
- BBa_K2656004: theJ23106 promoter in its Golden Braid compatible version from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Part Collection]
- BBa_K2656009: theB0030 ribosome biding site in its Golden Braid compatible version from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Part Collection]
- BBa_K2656013: This part.
- BBa_K2656026: theB0015 transcriptional terminator in its Golden Braid compatible version from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Part Collection]
In order to carry out a correct characterization of the protein and to be able to use it to make measurements of the different transcriptional units that we have assembled with it, we have obtained the emission and excitation spectra in the conditions of our equipment. To do this, we have used the transcriptional unit BBa_K2656100 assembled in a Golden Braid alpha1 plasmid(REF). By using this protocol (REF) with the parameters of Table 1, Figure 1 has been obtained.
Parameter | Value | ||
Number of samples | 6 | ||
Excitation Wavelength measurement range (nm) | [420-525] | ||
Emission wavelenght (nm) | 545 | ||
Emission Wavelength measurement range (nm) | [470-580] | ||
Excitation wavelenght (nm) | 450 | ||
Gain (G) | 50 | ||
Table 1. Parameters used to obtain the spectra |
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 14