Difference between revisions of "Part:BBa K1614014:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Cloned without restriction enzymes to avoid issues occurring from conserved cut sites. For more details see RFC 110. | + | Cloned without restriction enzymes to avoid issues occurring from conserved cut sites. For more details see RFC 110. |
− | + | This part was designed to quantify ATP concentration. To achieve this we exchanged stem two in the Spinach aptamer with an ATP binding aptamer. Now the Spinach can only become fluorescent in presence of ATP. We used this part in our measurement device described on our Wiki. With an appropriate tiration curve the concentration of ATP can directly be calculated of the fluorescent insensitivity. | |
− | + | ||
===Source=== | ===Source=== |
Latest revision as of 14:32, 20 September 2015
ATP Aptamer JAWS1 Spinach2
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 165
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 165
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 77
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 165
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 165
Illegal NgoMIV site found at 178
Illegal NgoMIV site found at 207 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Cloned without restriction enzymes to avoid issues occurring from conserved cut sites. For more details see RFC 110. This part was designed to quantify ATP concentration. To achieve this we exchanged stem two in the Spinach aptamer with an ATP binding aptamer. Now the Spinach can only become fluorescent in presence of ATP. We used this part in our measurement device described on our Wiki. With an appropriate tiration curve the concentration of ATP can directly be calculated of the fluorescent insensitivity.
Source
Synthentic created with JAWS with Spinach II aptamer (Babendure, J.R., Adams, S.R., and Tsien, R.Y. (2003). Aptamers switch on fluorescence of triphenylmethane dyes. Journal of the American Chemical Society 125, 14716-14717.) and ATP aptamer