Difference between revisions of "Part:BBa K3431042"
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<partinfo>BBa_K3431042 short</partinfo> | <partinfo>BBa_K3431042 short</partinfo> | ||
− | + | Toehold Switch with Invertase as Expression Protein (op21_B) is an RNA-based device that is to apply as a biosensor for miRNA. This biosensor is designed to detect and reflect the amount of miRNA-21 through the expression of Beta-Fructosidase (Thermotoga Maritima MSB8) (BBa_K3431000), which can convert sucrose into glucose in a time-saving process and its result can be easily represented in the readout of glucose meter. The mechanism for detection relied on the following part - Toehold Switch for miRNA-21 (op21_B) (BBa_K3431033) - whose restriction on the expression of invertase can be liberated upon binding with miRNA-21. Furthermore, we include T7 promoter (BBa_I719005) and terminator (BBa_K731721) to insure that our device can transcribe and translate in the environment of PURExpress in vitro protein synthesis kit. | |
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Revision as of 11:17, 18 October 2020
op21_B_ToeholdSwitch-Regulated Invertase
Toehold Switch with Invertase as Expression Protein (op21_B) is an RNA-based device that is to apply as a biosensor for miRNA. This biosensor is designed to detect and reflect the amount of miRNA-21 through the expression of Beta-Fructosidase (Thermotoga Maritima MSB8) (BBa_K3431000), which can convert sucrose into glucose in a time-saving process and its result can be easily represented in the readout of glucose meter. The mechanism for detection relied on the following part - Toehold Switch for miRNA-21 (op21_B) (BBa_K3431033) - whose restriction on the expression of invertase can be liberated upon binding with miRNA-21. Furthermore, we include T7 promoter (BBa_I719005) and terminator (BBa_K731721) to insure that our device can transcribe and translate in the environment of PURExpress in vitro protein synthesis kit.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1421
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1192
Illegal BamHI site found at 1322
Illegal XhoI site found at 1393 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 993
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 524