Plasmodium spp. and Leishmania are the causing parasites to malaria and leishmaniasis, two widely spread diseases that are still responsible for millions of cases worldwide every year. The proteins in study, AGAP007752-PA (Anopheles gambiae) and α-tubulin (Plasmodium spp. and Leishmania infantum), are thought to be relevant in decreasing parasite transmission by affecting their life cycles. The aim is to use recombinant versions of those proteins to develop new control strategies to diminish disease incidence. In order to further the AGAP007752-PA research, the gene was amplified, cloned and sequenced. After, all three proteins were expressed in E. coli, and the recombinant proteins analysed by SDS-PAGE and Western Blot, again verifying their identities by sequencing. After the procedures’ optimization, AGAP007752 gene amplification was achieved, although this protein was not successfully expressed. Contrarily, alfa-tubulins had been previously cloned, and the proteins’ expression was now achieved. The research can be furthered, either through the production of the recombinant protein (AGAP007752-PA) or through purification of the expressed recombinant α-tubulin proteins.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Plasmodium spp. and Leishmania are the causing parasites to malaria and leishmaniasis, two widely spread diseases that are still responsible for millions of cases worldwide every year. The proteins in study, AGAP007752-PA (Anopheles gambiae) and α-tubulin (Plasmodium spp. and Leishmania infantum), are thought to be relevant in decreasing parasite transmission by affecting their life cycles. The aim is to use recombinant versions of those proteins to develop new control strategies to diminish disease incidence. In order to further the AGAP007752-PA research, the gene was amplified, cloned and sequenced. After, all three proteins were expressed in E. coli, and the recombinant proteins analysed by SDS-PAGE and Western Blot, again verifying their identities by sequencing. After the procedures’ optimization, AGAP007752 gene amplification was achieved, although this protein was not successfully expressed. Contrarily, alfa-tubulins had been previously cloned, and the proteins’ expression was now achieved. The research can be furthered, either through the production of the recombinant protein (AGAP007752-PA) or through purification of the expressed recombinant α-tubulin proteins.
Catarina Patrício was born in 1991. In 2009 she started an undergratuate degree in Pharmacy, concluding it in 2015. This book is based on the research carried out for the said degree.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Plasmodium spp. and Leishmania are the causing parasites to malaria and leishmaniasis, two widely spread diseases that are still responsible for millions of cases worldwide every year. The proteins in study, AGAP007752-PA (Anopheles gambiae) and -tubulin (Plasmodium spp. and Leishmania infantum), are thought to be relevant in decreasing parasite transmission by affecting their life cycles. The aim is to use recombinant versions of those proteins to develop new control strategies to diminish disease incidence. In order to further the AGAP007752-PA research, the gene was amplified, cloned and sequenced. After, all three proteins were expressed in E. coli, and the recombinant proteins analysed by SDS-PAGE and Western Blot, again verifying their identities by sequencing. After the procedures' optimization, AGAP007752 gene amplification was achieved, although this protein was not successfully expressed. Contrarily, alfa-tubulins had been previously cloned, and the proteins' expression was now achieved. The research can be furthered, either through the production of the recombinant protein (AGAP007752-PA) or through purification of the expressed recombinant -tubulin proteins. 88 pp. Englisch. N° de réf. du vendeur 9783659781704
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Plasmodium spp. and Leishmania are the causing parasites to malaria and leishmaniasis, two widely spread diseases that are still responsible for millions of cases worldwide every year. The proteins in study, AGAP007752-PA (Anopheles gambiae) and ¿-tubulin (Plasmodium spp. and Leishmania infantum), are thought to be relevant in decreasing parasite transmission by affecting their life cycles. The aim is to use recombinant versions of those proteins to develop new control strategies to diminish disease incidence. In order to further the AGAP007752-PA research, the gene was amplified, cloned and sequenced. After, all three proteins were expressed in E. coli, and the recombinant proteins analysed by SDS-PAGE and Western Blot, again verifying their identities by sequencing. After the procedures' optimization, AGAP007752 gene amplification was achieved, although this protein was not successfully expressed. Contrarily, alfa-tubulins had been previously cloned, and the proteins' expression was now achieved. The research can be furthered, either through the production of the recombinant protein (AGAP007752-PA) or through purification of the expressed recombinant ¿-tubulin proteins.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 88 pp. Englisch. N° de réf. du vendeur 9783659781704
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Plasmodium spp. and Leishmania are the causing parasites to malaria and leishmaniasis, two widely spread diseases that are still responsible for millions of cases worldwide every year. The proteins in study, AGAP007752-PA (Anopheles gambiae) and -tubulin (Plasmodium spp. and Leishmania infantum), are thought to be relevant in decreasing parasite transmission by affecting their life cycles. The aim is to use recombinant versions of those proteins to develop new control strategies to diminish disease incidence. In order to further the AGAP007752-PA research, the gene was amplified, cloned and sequenced. After, all three proteins were expressed in E. coli, and the recombinant proteins analysed by SDS-PAGE and Western Blot, again verifying their identities by sequencing. After the procedures' optimization, AGAP007752 gene amplification was achieved, although this protein was not successfully expressed. Contrarily, alfa-tubulins had been previously cloned, and the proteins' expression was now achieved. The research can be furthered, either through the production of the recombinant protein (AGAP007752-PA) or through purification of the expressed recombinant -tubulin proteins. N° de réf. du vendeur 9783659781704
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Taschenbuch. Etat : Neu. Recombinant Protein Production: A Case Study Research Report | Catarina Patrício (u. a.) | Taschenbuch | 88 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659781704 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu Print on Demand. N° de réf. du vendeur 104156095
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