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Construction of pEGFP-C1/U6-mediated plasmid expressing MDR1 shRNA / 中国实验血液学杂志
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-280660
Biblioteca responsável: WPRO
ABSTRACT
To construct a plasmid expressing MDR1 short hairpin RNA (shRNA) mediated by pEGFP-C1/U6 vector, two coding sequences of 19 nucleotides were selected from MDR. Two pairs of oligonucleotides were designed for these two fragments. After annealing the formed double-stranded DNAs were ligated with plasmid pEGFP-C1/U6 (pEGFP-C1 vector with U6 promoter). The plasmids producing MDR1 shRNA were constructed from the inverted motif containing 9 spacers and four Ts. The results showed that the constructed plasmids were named pEGFP-C1/U6/A and pEGFP-C1/U6/B, and the constructs were identified by restriction and sequence analysis, no any base mutation was observed. It is concluded that plasmids of pEGFP-C1/U6/A and pEGFP-C1/U6/B expressing MDR1 shRNA were successfully constructed, providing a highly effective method for reversing the multidrug resistance in clinic.
Assuntos
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Plasmídeos / RNA Mensageiro / RNA Nuclear Pequeno / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / RNA Interferente Pequeno / Proteínas de Fluorescência Verde / Proteínas de Ligação a DNA / Vetores Genéticos Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2006 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Plasmídeos / RNA Mensageiro / RNA Nuclear Pequeno / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / RNA Interferente Pequeno / Proteínas de Fluorescência Verde / Proteínas de Ligação a DNA / Vetores Genéticos Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2006 Tipo de documento: Artigo
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