000 04847nam a22003975i 4500
999 _c392714
_d392714
_x1
001 392714
003 ES-MaUEC
005 20240314174258.0
006 a|||| o|||| 00| 0
007 cr nn 008mamaa
008 100301s2003 xxu| o |||| 0|eng d
020 _a9781592593590
024 7 _a10.1385/1592593593
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aQP624.5 .A57
_b2003 EB
245 0 0 _aGeneration of cDNA Libraries :
_bMethods and Protocols
_cedited by Shao-Yao Ying
250 _a1st edition 2003
264 1 _aTotowa, NJ
_bHumana Press
_c2003
300 _a1 recurso en línea (XIV, 338 páginas)
336 _atexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
347 _aarchivo de texto
_bPDF
490 0 _aMethods in Molecular Biology
_x1940-6029
_v221
505 0 _aComplementary DNA Libraries -- Rapid Amplification of cDNA Ends -- cDNA Generation on Paramagnetic Beads -- Construction of a Normalized cDNA Library by mRN-cDNA Hybridization and Subtraction -- Amplification of cDNA Ends Using PCR Suppression Effect and Step-Out PCR -- Use of Inverse PCR to Clone cDNA Ends -- Construction of Size-Fractionated cDNA Library Assisted by an In Vitro Recombination Reaction -- Construction of a Full-Length Enriched and a 5?-End Enriched cDNA Library Using the Oligo-Capping Method -- cDNA Library Construction Using In Vitro Transcriptional Amplification -- Amplification of Representative cDNA Pools from Microscopic Amounts of Animal Tissue -- Single-Cell cDNA Library Construction Using Cycling aRNA Amplification -- mRNA/cDNA Library Construction Using RNA-Polymerase Cycling Reaction -- Quality Assessment of cDNA Libraries -- Assessment of the Quality of mRNA Libraries by Agarose Gel Electrophoresis -- PACS RT-PCR -- Single-Cell mRNA Library Analysis by Northern Blot Hybridization -- Generation of cDNA Libraries for Profiling Gene Expression of Given Tissues or Cells -- Screening Poly [dA/dT(?)] cDNA for Gene Identification -- Generation of Longer cDNA Fragments from SAGE Tags for Gene Identification -- Generation of Full-Length cDNA Libraries Enriched for Differentially Expressed Genes -- Subtractive Hybridization for the Identification of Differentially Expressed Genes Using Uraci-DNA Glycosylase and Mung-Bean Nuclease -- Subtractive Cloning of Differential Genes Using RNA-PCR -- Strategy for Construction of a cDNA Encoding a Repetitive Amino Acid Sequence -- Preparing Lambda Libraries for Expression of Proteins in Prokaryotes or Eukaryotes -- Peptide Library Construction from RNA-PCR-Derived RNAs -- Identifying Interacting Proteins in an Escherichia coli-Based Two-Hybrid System -- Future Perspectives.
520 _aWith the decoding of the human genome and the potential application of its information to gene chips, the ability to generate cDNA libraries for functional assays of specific gene sequences has become critical in gene manipulation and genetic research. In Generation of cDNA Libraries: Methods and Protocols, expert researchers and inventors in the field describe their own proven techniques for generating cDNA/mRNA libraries to identify the functions of specific decoded gene sequences. A wide variety of techniques is presented for enhancing the generation of complete and full-length libraries, and for confirming the quality of the cDNAs generated. Among the applications detailed are electrophoresis, Northern blotting, single-cell microarray analysis, subtractive hybridization, subtractive cloning, gene cloning, and peptide library generation. Each method includes background information, step-by-step instructions, a list of reagents, operational tips, and notes on instrumentation. A background tutorial provides essential information: the definition of a cDNA library, the various types of cDNA libraries, the differences between methods for cDNA library generation using either conventional approaches or novel strategies, and the quality of cDNA libraries. State-of-the-art and highly practical, Generation of cDNA Libraries: Methods and Protocols provides a variety of powerful and readily reproducible techniques for the generation of the entire range of complete, full-length cDNA/mRNA libraries needed in today's forefront genetic research.
988 _aSpringer_Protocols_2003
650 7 _2embne
_9140525
_aÁcidos nucleicos
776 0 8 _iPrinted edition:
_z9781617373336
776 0 8 _iPrinted edition:
_z9781489938428
776 0 8 _iPrinted edition:
_z9781588290663
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/1592593593
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b01/2024
_dz
_eIG
_zSI