RU2009126233A - Recombinant plasmid DNA pQe30_PS-CFP2 / TurboYFP_MBP7, coding fragment of human myelin basic protein fused 80-104 IN THE COMPOSITION OF STRUCTURES with yellow and cyan fluorescent protein EPeFRET, STRAIN Escherichia coli BL21 (DE3) - PRODUCER said protein, AND METHOD OF PRODUCING RECOMBINANT PROTEIN EPeFRET - Google Patents

Recombinant plasmid DNA pQe30_PS-CFP2 / TurboYFP_MBP7, coding fragment of human myelin basic protein fused 80-104 IN THE COMPOSITION OF STRUCTURES with yellow and cyan fluorescent protein EPeFRET, STRAIN Escherichia coli BL21 (DE3) - PRODUCER said protein, AND METHOD OF PRODUCING RECOMBINANT PROTEIN EPeFRET Download PDF

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RU2009126233A
RU2009126233A RU2009126233/10A RU2009126233A RU2009126233A RU 2009126233 A RU2009126233 A RU 2009126233A RU 2009126233/10 A RU2009126233/10 A RU 2009126233/10A RU 2009126233 A RU2009126233 A RU 2009126233A RU 2009126233 A RU2009126233 A RU 2009126233A
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protein
cfp2
epefret
mbp7
turboyfp
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RU2009126233/10A
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Russian (ru)
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RU2430161C2 (en
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Александр Габибович Габибов (RU)
Александр Габибович Габибов
Алексей Анатольевич Белогуров (RU)
Алексей Анатольевич Белогуров
Наталья Александровна Пономаренко (RU)
Наталья Александровна Пономаренко
Мария Юрьевна Захарова (RU)
Мария Юрьевна Захарова
Анатолий Иванович Мирошников (RU)
Анатолий Иванович Мирошников
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Учреждение Российской академии наук Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН (RU)
Учреждение Российской академии наук Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН
Российская Федерация, от имени которой выступает Федеральное агентство по науке и инновациям (RU)
Российская Федерация, от имени которой выступает Федеральное Агентство по науке и инновациям
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Priority to RU2009126233/10A priority Critical patent/RU2430161C2/en
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Abstract

1. Рекомбинантная плазмидная ДНК pQe30_PS-CFP2/TurboYFP_MBP7 размером 4916 п.о., кодирующей гибридный белок PS-CFP2 и YSP, содержащий пептид основного белка миелина 80-104 состоящей из: !фрагмента ДНК, приведенного на рис.1, содержащего промотор транскрипции Т5 РНК-полимеразы, участок связывания рибосомы; ! фрагмента ДНК плазмиды ген β-лактамазы, детерминирующий устойчивость трансформированных плазмидой pQe30_PS-CFP2/TurboYFP_MBP7 клеток Escherichia coli к ампициллину, в качестве генетического маркера. ! 2. Штамм Escherichia coli BL21(DE3)/pQe30_PS-CFP2/TurboYFP_MBP7 - продуцента гибридного белка EPeFRET, содержащего пептид основного белка миелина 80-104. ! 3. Способ получения белка EPeFRET, включающего культивирование штамма-продуцента Escherichia coli BL21(DE3)/ PS-CFP2/TurboYFP MBP7, разрушение клеток и его очистку методами аффинной и гель-проникающей хроматографии. 1. Recombinant plasmid DNA pQe30_PS-CFP2 / TurboYFP_MBP7, 4916 bp in size, encoding the fusion protein PS-CFP2 and YSP, containing the peptide of the main myelin protein 80-104 consisting of:! The DNA fragment shown in Fig. 1, containing the transcription promoter T5 RNA polymerase, ribosome binding site; ! of the plasmid DNA fragment, the β-lactamase gene, which determines the resistance of ampicillin to Escicichia coli transformed with the plasmid pQe30_PS-CFP2 / TurboYFP_MBP7, as a genetic marker. ! 2. The strain Escherichia coli BL21 (DE3) / pQe30_PS-CFP2 / TurboYFP_MBP7 - producer of the hybrid protein EPeFRET containing the peptide of the main protein myelin 80-104. ! 3. A method of producing an EPeFRET protein, comprising culturing a producer strain of Escherichia coli BL21 (DE3) / PS-CFP2 / TurboYFP MBP7, destroying cells and purifying them by affinity and gel permeation chromatography.

Claims (3)

1. Рекомбинантная плазмидная ДНК pQe30_PS-CFP2/TurboYFP_MBP7 размером 4916 п.о., кодирующей гибридный белок PS-CFP2 и YSP, содержащий пептид основного белка миелина 80-104 состоящей из:1. Recombinant plasmid DNA pQe30_PS-CFP2 / TurboYFP_MBP7 with a size of 4916 bp encoding a fusion protein PS-CFP2 and YSP containing a peptide of the main protein myelin 80-104 consisting of: фрагмента ДНК, приведенного на рис.1, содержащего промотор транскрипции Т5 РНК-полимеразы, участок связывания рибосомы;the DNA fragment shown in Fig. 1 containing the T5 RNA polymerase transcription promoter, the ribosome binding site; фрагмента ДНК плазмиды ген β-лактамазы, детерминирующий устойчивость трансформированных плазмидой pQe30_PS-CFP2/TurboYFP_MBP7 клеток Escherichia coli к ампициллину, в качестве генетического маркера.of the plasmid DNA fragment, the β-lactamase gene, which determines the resistance of ampicillin to Escicichia coli transformed with the plasmid pQe30_PS-CFP2 / TurboYFP_MBP7, as a genetic marker. 2. Штамм Escherichia coli BL21(DE3)/pQe30_PS-CFP2/TurboYFP_MBP7 - продуцента гибридного белка EPeFRET, содержащего пептид основного белка миелина 80-104.2. The strain Escherichia coli BL21 (DE3) / pQe30_PS-CFP2 / TurboYFP_MBP7 - producer of the hybrid protein EPeFRET containing the peptide of the main protein myelin 80-104. 3. Способ получения белка EPeFRET, включающего культивирование штамма-продуцента Escherichia coli BL21(DE3)/ PS-CFP2/TurboYFP MBP7, разрушение клеток и его очистку методами аффинной и гель-проникающей хроматографии. 3. A method of producing an EPeFRET protein, comprising culturing a producer strain of Escherichia coli BL21 (DE3) / PS-CFP2 / TurboYFP MBP7, destroying cells and purifying them by affinity and gel permeation chromatography.
RU2009126233/10A 2009-07-09 2009-07-09 RECOMBINANT PLASMID DNA pQe30_PS-CFP2/TurboYFP_MBP7, CODING PROTEIN PS-CFP2/TurboYFP_MBP7, STRAIN OF Escherichia coli BL21(DE3)/pQe30_PS-CFP2/TurboYFP_MBP7 - SAID PROTEIN PRODUCENT AND METHOD OF OBTAINING PROTEIN PS-CFP2/TurboYFP_MBP7 RU2430161C2 (en)

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RU2009126233/10A RU2430161C2 (en) 2009-07-09 2009-07-09 RECOMBINANT PLASMID DNA pQe30_PS-CFP2/TurboYFP_MBP7, CODING PROTEIN PS-CFP2/TurboYFP_MBP7, STRAIN OF Escherichia coli BL21(DE3)/pQe30_PS-CFP2/TurboYFP_MBP7 - SAID PROTEIN PRODUCENT AND METHOD OF OBTAINING PROTEIN PS-CFP2/TurboYFP_MBP7

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RU2009126233/10A RU2430161C2 (en) 2009-07-09 2009-07-09 RECOMBINANT PLASMID DNA pQe30_PS-CFP2/TurboYFP_MBP7, CODING PROTEIN PS-CFP2/TurboYFP_MBP7, STRAIN OF Escherichia coli BL21(DE3)/pQe30_PS-CFP2/TurboYFP_MBP7 - SAID PROTEIN PRODUCENT AND METHOD OF OBTAINING PROTEIN PS-CFP2/TurboYFP_MBP7

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RU2679055C2 (en) * 2016-12-29 2019-02-05 Федеральное государственное бюджетное учреждение науки институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова Российской академии наук (ИБХ РАН) RECOMBINANT PLASMID DNA POPTIVEC-MBP84-106-Fc ENCODING CONSTANT FRAGMENT OF HUMAN IMMUNOGLOBULIN FUSED WITH FRAGMENT OF MYELIN BASIC PROTEIN, EUKARYOTIC CELL LINES - PRODUCERS OF SPECIFIED PROTEIN AND METHOD FOR OBTAINING MBP84-106-Fc PROTEIN FOR MULTIPLE SCLEROSIS THERAPY
RU2691308C1 (en) * 2018-08-20 2019-06-11 Федеральное государственное бюджетное научное учреждение Федеральный исследовательский центр "Институт цитологии и генетики Сибирского отделения Российской академии наук" (ИЦиГ СО РАН) BACTERIAL STRAIN ESCHERICHIA coli/pTdcR-turboYFP, HAVING SENSITIVITY TO TERAHERTZ RADIATION

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