Difference between revisions of "Part:BBa K1955003"
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<b style="font-size:23px;">pSB1C3-5'HYG</b><br><br> | <b style="font-size:23px;">pSB1C3-5'HYG</b><br><br> | ||
− | We selected the 5'- untranslated region of a highly expressed gene | + | We selected the 5'-untranslated region (UTR) of a highly expressed gene p36 because the 5’UTR stabilizes the mRNA for constitutive expression in both Leishmania stages. We also added a hygromycin-resistant gene as a drug selection marker. This dual-function biobrick enables the regulation of protein expression and drug selection. The 3'UTR serves as the terminator for protein expression in Leishamnia. This system is most commonly and effectively used in Leishmania experiments. Users can insert any protein sequence between the Leish-5'UTR-HYG and Leish-3'UTR for your target protein expression in Leishmania.<br><br> |
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<b style="font-size:20px;">(1) The basic part checked by PCR: </b> | <b style="font-size:20px;">(1) The basic part checked by PCR: </b> |
Revision as of 10:31, 4 December 2016
pSB1C3-5'HYG
We selected the 5'-untranslated region (UTR) of a highly expressed gene p36 because the 5’UTR stabilizes the mRNA for constitutive expression in both Leishmania stages. We also added a hygromycin-resistant gene as a drug selection marker. This dual-function biobrick enables the regulation of protein expression and drug selection. The 3'UTR serves as the terminator for protein expression in Leishamnia. This system is most commonly and effectively used in Leishmania experiments. Users can insert any protein sequence between the Leish-5'UTR-HYG and Leish-3'UTR for your target protein expression in Leishmania.
(1) The basic part checked by PCR:
We used pSB1C3-5’HYG, pSB1C3-3’UTR, pSB1C3-HA, pSB1C3-OVA as template, to check the length of the inserts. The PCR reaction was performed with Taq polymerase, and screened in 0.8% agarose gel by electrophoresis.
Sequence and Features