Construction of plasmid expression vector for specific peptide of the rubella virus E1 gene / 中华男科学杂志
National Journal of Andrology
; (12): 318-321, 2009.
Article
Dans Zh
| WPRIM
| ID: wpr-292379
Responsable en Bibliothèque :
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To construct a recombinant plasmid vector of the RV specific fragment for expressing the specific fragment of RV E1 protein.</p><p><b>METHODS</b>RNA of the RV attenuated live vaccine Wistar RA27/3 strain was extracted and reversely transcribed. The specific fragment of the E1 gene was amplified and the PCR products cloned in the vector pGEX-2T after purification. Positive clones were selected and identified by two-enzyme digestion and sequence analysis.</p><p><b>RESULTS</b>A 330 bp target fragment was successfully cloned, and the sequence of the recombinant plasmid was consistent with the original sequence.</p><p><b>CONCLUSION</b>Successful cloning of the RV El specific fragment and the construction of the recombinant plasmid have laid a foundation for further expressing the recombinant protein.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Plasmides
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Virus de la rubéole
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ARN viral
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Données de séquences moléculaires
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Séquence nucléotidique
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Expression des gènes
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Protéines de l'enveloppe virale
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Clonage moléculaire
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RT-PCR
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Allergie et immunologie
langue:
Zh
Texte intégral:
National Journal of Andrology
Année:
2009
Type:
Article