Difference between revisions of "Part:BBa K4414005"
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<partinfo>BBa_K4414005 short</partinfo> | <partinfo>BBa_K4414005 short</partinfo> | ||
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==Usage and Biology== | ==Usage and Biology== | ||
− | + | There is an extensive use of fluorescent bioimaging in the fields of biochemistry, biotechnology, cell and developmental biology. In comparison with other fluorescent tags, GFP-like proteins have the advantage of forming internal chromophore without requiring accessory cofactors, enzymes or substrates other than molecular oxygen, making possible chromophore formation in live organisms, tissues and cells(Stepanenko et al., 2008;Cubitt et al., 1995). We obtained this DNA by DNA synthesis.This part can be used in level 1 biological laboratory. | |
− | There is an extensive use of fluorescent bioimaging in the fields of biochemistry, biotechnology, cell and developmental biology. In comparison with other fluorescent tags, GFP-like proteins have the advantage of forming internal chromophore without requiring accessory cofactors, enzymes or substrates other than molecular oxygen, making possible chromophore formation in live organisms, tissues and cells | + | |
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===Reference=== | ===Reference=== | ||
− | + | 1.Cubitt, A. B., Heim, R., Adams, S. R., Boyd, A. E., Gross, L. A., & Tsien, R. Y. (1995). Understanding, improving and using green fluorescent proteins. Trends in Biochemical Sciences, 20(11), 448–455. https://doi.org/10.1016/s0968-0004(00)89099-4. | |
− | + | 2.Stepanenko, O. V., Verkhusha, V. V., Kuznetsova, I. M., Uversky, V. N., & Turoverov, K. K. (2008). Fluorescent Proteins as Biomarkers and Biosensors: Throwing Color Lights on Molecular and Cellular Processes. Current Protein & Peptide Science, 9(4), 338–369. |
Latest revision as of 03:49, 14 October 2022
GFP
Usage and Biology
There is an extensive use of fluorescent bioimaging in the fields of biochemistry, biotechnology, cell and developmental biology. In comparison with other fluorescent tags, GFP-like proteins have the advantage of forming internal chromophore without requiring accessory cofactors, enzymes or substrates other than molecular oxygen, making possible chromophore formation in live organisms, tissues and cells(Stepanenko et al., 2008;Cubitt et al., 1995). We obtained this DNA by DNA synthesis.This part can be used in level 1 biological laboratory.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Functional characterization
We connect GFP as a reporter gene to other sequences encoding proteins, as shown in the figure is the fluorescence image of GFP.
Figure 1.The picture of fluorescence diagram
Reference
1.Cubitt, A. B., Heim, R., Adams, S. R., Boyd, A. E., Gross, L. A., & Tsien, R. Y. (1995). Understanding, improving and using green fluorescent proteins. Trends in Biochemical Sciences, 20(11), 448–455. https://doi.org/10.1016/s0968-0004(00)89099-4.
2.Stepanenko, O. V., Verkhusha, V. V., Kuznetsova, I. M., Uversky, V. N., & Turoverov, K. K. (2008). Fluorescent Proteins as Biomarkers and Biosensors: Throwing Color Lights on Molecular and Cellular Processes. Current Protein & Peptide Science, 9(4), 338–369.