Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống
1
/ 268 trang
THÔNG TIN TÀI LIỆU
Thông tin cơ bản
Định dạng
Số trang
268
Dung lượng
24,16 MB
Nội dung
METHODS IN MOLECULAR BIOLOGY John M. Walker, Series Editor 178.'Antihody Phage Display: Mrrhods old Pr~~coro/.\. edited hy 177. Two-Hyhrid Systems: Mrrhoh arrdProroco1.i. edited b) Purr1 176. Steroid Receptor Methods: Pf',J/~JCll/S n~rd ASSO~S. edited hy 175. Genomics Protocols. edlted by M~clrcrrl P SfarAry urltl 171. Epstein-Barr Virus Protocols, edited hy JiJ[lJlJrU B. Wilso~l 173. Calcium-Binding Protein Protocols, Volume 2: Mrrhods om/ 172. Calcium-Binding Protein Protocols, Volume 1: Rer,iew cm/ 171. Proteoglycan Protocols, edited by Rewro 1'. 2001 170. DNA Arrays: Mcrhorls rurd Plororols, edited hy Joyy 8. 169. Neurotrophin Protocols, edited by Roberr A. Rlrsh. 2001 IhX. Protein Structure, Stability, and Folding, edited hy Krurlerh 167. DNA Sequencing Protocols. Se'.od Edirml, ediled hy Co1irr 166. lmmunoloxin Methods and Protocols. ed~ted by ll'rrlrrr A. 165. SV40 Protocols. edited by Ldo Rqm, 2lJlll 161. Kinesin Protocols, edited hy 1sdwllP VrrJws, ?001 163. Capillar) Electrophoresis of Kucleic Acids, Volume 2: P,o[.rr[.ol A/~/~lic~~rr~~~r\ uJCupi11or~ E/r~~/ro~~~l~nre.sr.s, edited hy Ktrrh R. Mirclrelso~r ond Jirq Clrorg, 2001 162. Capillary Electrophoresis of Nucleic Acids, Volume 1: /nrrodrrrriofr ro fhe Cupi//urr E1trrruphorrsi.s oj'i\'~rr/ur Arrds, edited by Krrrlr R. ilfrrclre/.sorr mrd Jiq Chrrr,y. 2001 161. Cytoskeleton Methods and Protocols, edited by Rrry H. Covin, 2001 160. Nuclease hlethods and Protocols, edited by Cur1wrw H. Srhrin. 2001 159. Amino Acid Analysis Protocols, edited by Curhcrirre Cuupcr, Niwdr Prrckcr, arrd K~J IVi//im~, ZOO1 ISY. Gene Knockoout Protocols, edited by Mllrrrn J. T~IIIIIIS rlad /SIIIUI/ Kola, 2001 157. Mycotoxin Protocols, edited hy Murr IV. Trrr[bes.sa~rdi\lherr E. Pohluncl. 2001 156. Antigen Processing and Presentation Protocols, edited by JIJ~CU C. Solhtiru, 2001 155. Adipose Tissue Protocols, edited by G<rurdAi//wrrd, 2000 154. Connexin Methods and Protocols, edited hy Rohrrro 153 Neuropeptide Y Protocols. edited by Ambikarpaknn 152. DNA Repair Protocols: Protor!.ofrr S,v.sr~vtls. edited by I5 I. Matrix Metalloproteinaw Protocols, edited by hrr M. Clurk. 2001 150. Cumplement Methods and Protocols, edited by B. Pad 149. The ELlSA Guidebook, edited by John R. Crcnrhr, 2000 P/ri/ippu M. O'HrreIl and Roherc Arrten. 2001 N. MnrDrurtrld, 2001 Rrnlumn A. Lwb~wrun. 2001 Rmdr E~Is~~~u~II, ?(l(lI om/ Gcdtortl H. IV. Mny, 2001 Tdrnrqws. edited hy HUIIS J. Voxul. 21101 Cw Hi.\rorirr. edited by Huns J. l'o,yr/, 2001 Rurtlpul. ZOO/ P. Mllr/llr!., 2001 A. C~~IUIII und A/isuu I. M. Hill. 2001 Hull. 2001 8rrc::onc ond Clmriun Giurrslt~, 2UU1 flaf~~s~~br~~~~r~~~~r~~~lr, 20011 Purrd Vo'rrrrghon 2000 Morgurl, 2000 118. DNA-Protein Interactions: Principle.\ urrdProrucolr (2nd ed.). edited by Trnn Moss. 2001 117. Affinity Chromatography: Mrrhods und Prororols. edited hy Ptr.\ro/ Hailon. George K. Ehrlirh, \\'e!r-Jiu~r FIIII,~, nnd IVWfyu~rg 8ur//w/d, 2000 116. Mass Spectrometry of Proteins and Peptides, edlted by JoBrl 145. Bacterial Toxins: ~MPthodsandProtorols. edited by Orm Hdsr. 141. Calpain hlethods and Protocols. edited hy JlJhll S. Eke. ?fJO0 143. Protein Structure Prediction: Merhods und Pm/fIIYJ/S. 142. Transforming Growth Factor-Beta Protocols. edited hy Phi1ip 111. Plant Hormone Prutucols. edited by Grqor! A. Trdrr md 140. Chaperonin Protocols. edited by Clrrlurrw Schrrrrdu. 2UO0 139. Extracellular Matrix Protocols. cdited by Charks Srrerdi UII~ 138. Chemokine Protucols. edited hy Anrundu E. 1. Prodfour, Tiwrhr 137. Developmental Biology Protocols, Volume 111. edited by 136. Developmental Biology Protocols, Volume 11, edlted by Rodr 135. Developmental Biology Protocols, Volume I, edited by Rodr 134. T Cell Protocols: 1)nc~/up111rrrr urd Acrivurion. edited hy Kc,//! 133. Gene Targeting Protocols, edited by E~IC 8. KrrIrn 2001) 132. Bioinformatics Methods and Protocols, edited hy Srcph 131. Flavoprotein Protocols, edited by S. K. C~~IIIUII and G. A. 130. Transcription Factor Protocols, edited by ~MWIII J. ~:VJIII~IS, 129. Integrin Protocols, edited hy Ar~rkony Hon.lerr, IYYY 128. NMDA Protocols, edited by Mill Li. IYYY 127. Molecular Methods in Developmental Biology: Xenopus om1 Zehrujisk. edited by Mafrhm Gdlr, 1999 126. Adrenergic Receptor Protocols, edited by Cruris A. Morlrrda, 2ooO 125. Glycoprotein Methods and Protocols: Tltr bf~rcrrls, editcd hy 124. Protein Kinase Protocols, edited by Alusfnv D. Rrrrlr, 2001 123. In Siru Hybridization Protocols (2nd ed.), edited hy loll A. Durb,v 2000 122. Confocal Microscopy Methods and Protocols, edited by Sreph IV. Paddd 1999 121. Natural Killer Cell Protocols: Cellrrlor om/ Molerelor Merkods, edited by Ken.! S. Cunlpbell crd Marco Cdunnu, 2000 120. Eicosanoid Protocols, edited by Elias A. Linno.s, 1YYY 119. Chromatin Protocols, edited hy Perer 8. Hrckrr. 1YYY I IX. RNA-Protein Interaction Protocols, edited by S~rrarr R. 117. Electron Microscopy Methods and Protocols, edited hy M. n. ~~laplflclrl. 2000 20011 edited hy Duvrd Welnrrr. X100 H. How,, ?OW Jrremr A. Roberr,. 20011 Michael Grunr. 2000 A'. C \Vd/.s, rwd Chrrsrm, Powr. Zoo0 Roc!,! S. 7rm und Crrilin IV. Lo. 2000 S. Trrolr on(/ Crcilirr IV. Lo, 2000 S. Tlrun mrl Cecrliu IV. Lo. 2000 P Ke(rr.w. 2000 Misewr urd Sfephcw A. Knuvtr;. 2000 Rtid, 1YYY 2000 dtl/hwl~ P. C~lr/it,/d, 200fJ Hoyrlcs. lYYY A, Nasser Hujihuxlrerr, 1Y9Y DNA Arrays Methods andProtocols Edited by Jang B. Rampal Beckman Coulter, Inc., Fullerton, CA Humana Press Totowa, New Jersey [...]... concentration of RNAs in From: Methods in Molecular Biology, vol 170: DNA Arrays: Methods andProtocols Edited by: J B Rampal 0 Humana Press Inc., Totowa, NJ 1 2 Southern solution These were early forerunners of the current application of DNA microarrays to the analysis of sequence diversity and levels of gene expression In the late 196Os, Pardue and Gall (5) and Jones and Robertson (6) discovered a... interactions between the arrayed macromolecules and the test molecule of interest Classical examples of such recognition reactions are the interactions between the two complementary strands of a double-helical DNA molecule, betweena single-stranded DNA stretch and the messenger RNA copied fromit during transcription, between an antigen and an antibody, and between small ligands and their nucleic acid... Molecular Biology in Moscow and the Biochip Technology Center at Argonne National Laboratory, Argonne, IL ' From: Methods In Molecular Biology vol 170: DNA Arrays: Methods andProtocols Edited by: J 6.Rampal 0Humana Press Inc Totowa, NJ 17 18 Zlatanova and Mirzabekov 2 General Description of the MAGIChip" Technology MAGIChips'rM (Micro Arrays of Gel-Immobilized Compounds on a Chip) are arrays that we have... any position in the array Reprogramming the system to make a different array is simply a matter of changing the sequence file The oxidation and deprotection steps and the washes are common each cycle and are carried out flooding to by the whole surface with an excess of reagent or solvent Thus, the method is flexible and makes economical useof the most expensive reagents DNA Microarrays 7 As would be... complementary DNA microarray Science 270,467-470 (comments) DNA Microarrays 15 5 1 Shalon, D., Smith, S J and Brown, P 0 ( 1 996) A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization Genntne Res 6, 639-645 52 Lockhart, D J., Dong, H Byme, M C., Follettie, M.T., Gallo, M V., Chee, M S., Mittmann, M., Wang, C.,Kobayashi, M., Horton, H., and Brown, E...Contributors xi 1 DNA Microarrays History and Overview Edwin M Southern 1 Introduction 1.1 From Double Helix to Dot Blots It may seem premature to be writing a history DNA microarrays because of this technology is relatively new and clearly has more of a future than a past However readers could benefit from learning something about the technical basis of DNA microarrays, and younger readers be... following the introduction of fluorescent probes) The method used to fix chromosomes and nuclei to microscope slides in a way that allowed the DNA to take part in duplex formation with the probe is now used to fix DNA spotted on to slides in one microarray methodAnd the multicolor fluorescent labeling techniques introduced by Ried et al (7) and Balding and Ward(8),for the analysis of multiple probes FISH,... J., Hood, L., and Landegren, U ( 1 990) Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay Proc Nutl Acad Sci USA 87,8923-8927 49 Pastinen, T., Kurg, A., Metspalu, A., Peltonen, L., and Syvanen, A C (1997) Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays Genome Res 7,606-614 P 0 50 Schena, M., Shalon, D., Davis, R.W., and Brown, (1995)... accurately the positions of the spots and to know in advance their precise shape and size, and an additional, major advantage of glass or plastic supports is their dimensional stability and rigidity Permeable membranes swell in solvent and tendto shrink and distort when dried; their fragility and flexibility make it difficult to register their position during spotting and reading Thus, it is not possible... hybridization to high-density oligonucleotide arrays Nut Biotechnol 14, 1675- 1680 (comments) 2 Gel-Immobilized Microarrays of Nucleic Acids and Proteins Production and Application for Macromolecular Research Jordanka Zlatanova and Andrei Mirzabekov 1 Introduction Biochips are small platforms with spatially arrayed macromolecules (or pieces thereof) that allow the collection and analysisof large amounts of biological . use for advanced research. The purpose of DNA Arrcrys: Methods and Protocols is to provide instruction in designing and constructing DNA arrays, as well as hybridizing them with biological. genes using labeled rRNA as probe and to measure the concentration of RNAs in From: Methods in Molecular Biology, vol. 170: DNA Arrays: Methods and Protocols Edited by: J. B. Rampal. Targeting Protocols, edited by E~IC 8. KrrIrn 2001) 132. Bioinformatics Methods and Protocols, edited hy Srcph 131. Flavoprotein Protocols, edited by S. K. C~~IIIUII and G. A.