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| 001 | 235206 | ||
| 003 | ES-VaUE | ||
| 005 | 20221220020651.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 100301s1998 xxu| s |||| 0|eng d | ||
| 020 | _a9781592595785 | ||
| 024 | 7 |
_a10.1385/0896034216 _2doi |
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| 040 |
_aES-MaUEC _bspa _cES-MaUEC |
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| 245 | 1 | 0 |
_aPichia Protocols _cedited by David R. Higgins, James Cregg. |
| 250 | _a1st edition 1998 | ||
| 264 | 1 |
_aTotowa, NJ _bHumana Press _c1998 |
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| 300 |
_a1 recurso en línea (XI, 270 páginas) _b |
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| 336 |
_atexto _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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_arecurso electrónico _bcr _2rdacarrier |
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| 347 |
_aarchivo de texto _bPDF |
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| 490 | 0 |
_aMethods in Molecular Biology _x1940-6029 _v103 |
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| 505 | 0 | _ato Pichia pastoris -- Classical Genetic Manipulation -- Transformation -- Small Vectors for Expression Based on Dominant Drug Resistance with Direct Multicopy Selection -- The Generation of Multicopy Recombinant Strains -- Isolation of Nucleic Acids -- Generation of Protease-Deficient Strains and Their Use in Heterologous Protein Expression -- Glycosylation Profiling of Heterologous Proteins -- High Cell-Density Fermentation -- Use of Pichia pastoris as a Model Eukaryotic System -- Secretion of Recombinant Human Insulin-Like Growth Factor I (IGF-I) -- Secretion of scFv Antibody Fragments -- Expression of Tetanus Toxin Fragment C -- Expression of EGF and HIV Envelope Glycoprotein -- Expression of an Integral Membrane Protein, the 5HT5A Receptor -- Localization of the myc-Tagged 5HT5A Receptor by Immunogold Staining of Ultrathin Sections. | |
| 520 | _aThe Pichia pastoris expression system has rapidly become one of the key protein expression systems used in commercial, academic, and government laboratories today. In Pichia Protocols, David Higgins and James Cregg compile for the first time an all-inclusive collection of powerful experimental procedures to manipulate Pichia pastoris for gene expression purposes. The methods-developed by world-class researchers in their own laboratories-contain detailed descriptions of available expression strains, as well as vectors, and step-by-step instructions for the construction of expression strains and for their use in the production of foreign proteins from shake-flask or fermentor cultures. General procedures for the purification of foreign proteins are also provided, along with protocols for analyzing foreign protein products for glycosylation and subcellular location. Pichia Protocols captures the collective expertise of the international P. pastoris scientific community in close detail. It conveys a breadth of experience that will permit any researcher in molecular biology to quickly construct an expression strain designed to produce a desired foreign protein, and to use this state-of-the-art molecular and cellular biological system successfully in every area of biological research today. | ||
| 700 | 1 |
_aHiggins, David R _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 700 | 1 |
_aCregg, James _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 776 | 0 | 8 |
_iPrinted edition: _z9781489928023 |
| 776 | 0 | 8 |
_iPrinted edition: _z9781489928016 |
| 776 | 0 | 8 |
_iPrinted edition: _z9780896034211 |
| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/0896034216 _z(usuarios Universidad Europea de Valencia) |
| 942 |
_2lcc _cLE |
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| 988 | _aSpringer_Protocols_1998 | ||
| 999 |
_c235206 _d235206 |
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