2016
DOI: 10.1007/s00604-016-2057-3
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CdTe quantum dots with green fluorescence generated by bioluminescence resonance energy transfer from aequorin

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Cited by 6 publications
(3 citation statements)
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“…Protein Expression and Purification. First, the apo-aequorin gene (GenBank entry AY601106 36 ) was amplified by Pf u DNA polymerase. The amplified fragment was digested by SalI and XhoI and then cloned into the pPROEX HTB expression vector.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…Protein Expression and Purification. First, the apo-aequorin gene (GenBank entry AY601106 36 ) was amplified by Pf u DNA polymerase. The amplified fragment was digested by SalI and XhoI and then cloned into the pPROEX HTB expression vector.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…Following induction of His-tagged protein expression by addition of 1 mM IPTG for 4 h at 20 °C, cells were harvested by centrifugation and lysed by sonication. Afterward, the recombinant protein was purified by Ni-NTA agarose column, as described previously …”
Section: Materials and Methodsmentioning
confidence: 99%
“…Afterward, the recombinant protein was purified by Ni-NTA agarose column, as described previously. 45 Preparation of Semisynthetic Aequorin. To generate semisynthetic aequorin from recombinant apoaequorin, the purified apoaequorin was diluted with 50 mM Tris buffer (pH 7.6) containing 5 mM EDTA (buffer 1).…”
Section: ■ Materials and Methodsmentioning
confidence: 99%