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Molecular Cloning
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Molecular Cloning, also known as Maniatis, has served as the foundation of technical expertise in labs worldwide for 30 years. No other manual has been so popular, or so influential.
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cshlpress.com/checkout.tpl?sku=934&action=mc4&typ2=mc4dotcom | <img> |
laskerfoundation.org/awards/2012_s_description.htm | Tom Maniatis wins Lasker |
occamstypewriter.org/trading-knowledge/2012/09/14/not-quite-... | 'Not Quite a Book Prize' |
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Внутренние ссылки главной страницы ( 248 ) | |
/index.php | Home |
index.php?prt=1 | Protocol 1: Preparation of Plasmid DNA by Alkaline Lysis with SDS: Minipreps |
index.php?prt=2 | Protocol 2: Preparation of Plasmid DNA by Alkaline Lysis with SDS: Maxipreps |
index.php?prt=3 | ) |
index.php?prt=4 | Protocol 4: Precipitation of DNA with Ethanol |
index.php?prt=5 | Protocol 5: Precipitation of DNA with Isopropanol |
index.php?prt=6 | Protocol 6: Concentrating and Desalting Nucleic Acids with Microconcentrators |
index.php?prt=7 | Protocol 7: Concentrating Nucleic Acids by Extraction with Butanol |
index.php?prt=8 | Protocol 8: Preparation of Single-Stranded Bacteriophage M13 DNA by Precipitation with Polyethylene Glycol |
index.php?prt=9 | Protocol 9: Plating Bacteriophage M13 |
index.php?prt=10 | Protocol 10: Growing Bacteriophage M13 in Liquid Culture |
index.php?prt=11 | Protocol 11: Preparation of Double-Stranded (Replicative Form) Bacteriophage M13 DNA |
index.php?prt=12 | Protocol 12: Isolation of High-Molecular-Weight DNA Using Organic Solvents to Purify DNA |
index.php?prt=13 | Protocol 13: Isolation of High-Molecular-Weight DNA from Mammalian Cells Using Proteinase K and Phenol |
index.php?prt=14 | Protocol 14: A Single-Step Method for the Simultaneous Preparation of DNA, RNA, and Protein from Cells and Tissues |
index.php?prt=15 | Protocol 15: Preparation of Genomic DNA from Mouse Tails and Other Small Samples |
index.php?prt=16 | Protocol 16: Rapid Isolation of Yeast DNA |
index.php?prt=17 | Protocol 17: Using Ethidium Bromide to Estimate the Amount of DNA in Bands after Electrophoresis through Minigels |
index.php?prt=18 | Protocol 18: Estimating the Concentration of DNA by Fluorometry Using Hoechst 33258 |
index.php?prt=19 | Protocol 19: Quantifying DNA in Solution with PicoGreen |
index.php?prt=20 | Protocol 1: Agarose Gel Electrophoresis |
index.php?prt=21 | Protocol 2: Detection of DNA in Agarose Gels by Staining |
index.php?prt=22 | Protocol 3: Polyacrylamide Gel Electrophoresis |
index.php?prt=23 | Protocol 4: Detection of DNA in Polyacrylamide Gels by Staining |
index.php?prt=24 | Protocol 5: Detection of DNA in Polyacrylamide Gels by Autoradiography |
index.php?prt=25 | Protocol 6: Alkaline Agarose Gel Electrophoresis |
index.php?prt=26 | Protocol 7: Imaging: Autoradiography and Phosphorimaging |
index.php?prt=27 | Protocol 8: Recovery of DNA from Agarose Gels Using Glass Beads |
index.php?prt=28 | Protocol 9: Recovery of DNA from Low-Melting-Temperature Agarose Gels: Organic Extraction |
index.php?prt=29 | Protocol 10: Isolation of DNA Fragments from Polyacrylamide Gels by the Crush and Soak Method |
index.php?prt=30 | Protocol 11: Southern Blotting |
index.php?prt=31 | Protocol 12: Southern Blotting: Simultaneous Transfer of DNA from an Agarose Gel to Two Membranes |
index.php?prt=32 | Protocol 13: Southern Hybridization of Radiolabeled Probes to Nucleic Acids Immobilized on Membranes |
index.php?prt=33 | : High-Efficiency Transformation |
index.php?prt=34 | : Ultracompetent Cells |
index.php?prt=35 | : Nanoparticle-Mediated Transformation |
index.php?prt=36 | by Electroporation |
index.php?prt=37 | Protocol 5: Cloning in Plasmid Vectors: Directional Cloning |
index.php?prt=38 | Protocol 6: Cloning in Plasmid Vectors: Blunt-End Cloning |
index.php?prt=39 | Protocol 7: Dephosphorylation of Plasmid DNA |
index.php?prt=40 | Protocol 8: Attaching Phosphorylated Adaptors/Linkers to Blunt-Ended DNAs |
index.php?prt=41 | Protocol 9: Cloning PCR Products: Addition of Restriction Sites to the Termini of Amplified DNA |
index.php?prt=42 | Protocol 10: Cloning PCR Products: Blunt-End Cloning |
index.php?prt=43 | Protocol 11: Cloning PCR Products: Making T Vectors |
index.php?prt=44 | Protocol 12: Cloning PCR Products: TA Cloning |
index.php?prt=45 | Protocol 13: Cloning PCR Products: TOPO TA Cloning |
index.php?prt=46 | Protocol 14: Screening Bacterial Colonies Using X-Gal and IPTG: -Complementation |
index.php?prt=47 | Protocol 1: Propagating Gateway Vectors |
index.php?prt=48 | Protocol 2: Generating an ORF Entry Clone and Destination Clone |
index.php?prt=49 | Protocol 3: Using Multisite LR Cloning to Generate a Destination Clone |
index.php?prt=50 | Protocol 1: Small-Scale Isolation of BAC DNA and Verification by PCR |
index.php?prt=51 | Protocol 2: Large-Scale Preparation and Linearization of BAC DNA |
index.php?prt=52 | Protocol 3: Examination of BAC DNA Quality and Quantity by Pulsed-Field Gel Electrophoresis |
index.php?prt=53 | Protocol 4: Two-Step BAC Engineering: Preparation of Shuttle Vector DNA |
index.php?prt=54 | Protocol 5: Preparation of the A Homology Arm (A-Box) and B Homology Arm (B-Box) |
index.php?prt=55 | Protocol 6: Cloning of the A and B Homology Arms into the Shuttle Vector |
index.php?prt=56 | Protocol 7: Preparation and Verification of the Recombinant Shuttle Vector |
index.php?prt=57 | Protocol 8: Electroporation of Competent BAC Host Cells with the Recombinant Shuttle Vector |
index.php?prt=58 | Protocol 9: Verification of Cointegrates and Selection of Resolved BAC Clones |
index.php?prt=59 | Protocol 10: One-Step BAC Modification: Preparation of Plasmids |
index.php?prt=60 | Protocol 11: Preparation of the A Homology Arm (A-Box) |
index.php?prt=61 | Protocol 12: Cloning of the A Homology Arm into Reporter-Shuttle Vector |
index.php?prt=62 | Protocol 13: Transformation of the BAC Host with the RecA Vector |
index.php?prt=63 | Protocol 14: Transfer of the Reporter Vector into BAC/RecA Cells and Selection of Cointegrates |
index.php?prt=64 | and Preparation of DNA |
index.php?prt=65 | Protocol 16: Small-Scale Preparations of Yeast DNA |
index.php?prt=66 | Protocol 1: Purification of Total RNA from Mammalian Cells and Tissues |
index.php?prt=67 | Protocol 2: Isolation of Total RNA from Zebrafish Embryos and Adults |
index.php?prt=68 | Protocol 3: Total RNA Isolation from Drosophila melanogaster |
index.php?prt=69 | Protocol 4: Total RNA Extraction from Caenorhabditis elegans |
index.php?prt=70 | Using Hot Acid Phenol |
index.php?prt=71 | Protocol 6: Quantifying and Storing RNA |
index.php?prt=72 | Protocol 7: Precipitation of RNA with Ethanol |
index.php?prt=73 | Protocol 8: Removing DNA Contamination from RNA Samples by Treatment with RNase-Free DNase I |
index.php?prt=74 | Messenger RNA Using Magnetic Oligo(dT) Beads |
index.php?prt=75 | Protocol 10: Separation of RNA according to Size: Electrophoresis of RNA through Agarose Gels Containing Formaldehyde |
index.php?prt=76 | Protocol 11: Separation of RNA according to Size: Electrophoresis of RNA through Denaturing Urea Polyacrylamide Gels |
index.php?prt=77 | Protocol 12: Transfer and Fixation of Denatured RNA in Agarose Gels to Membranes |
index.php?prt=78 | Protocol 13: Transfer and Fixation of Denatured RNA in Polyacrylamide Gels to Membranes by Electrophoretic Transfer |
index.php?prt=79 | Protocol 14: Northern Hybridization |
index.php?prt=80 | Protocol 15: Dot and Slot Hybridization of Purified RNA |
index.php?prt=81 | Protocol 16: Mapping RNA with Nuclease S1 |
index.php?prt=82 | Protocol 17: Ribonuclease Protection: Mapping RNA with Ribonuclease and Radiolabeled RNA Probes |
index.php?prt=83 | Protocol 18: Analysis of RNA by Primer Extension |
index.php?prt=84 | Protocol 1: The Basic Polymerase Chain Reaction |
index.php?prt=85 | Protocol 2: Hot Start PCR |
index.php?prt=86 | Protocol 3: Touchdown PCR |
index.php?prt=87 | Protocol 4: PCR Amplification of GC-Rich Templates |
index.php?prt=88 | Protocol 5: Long and Accurate PCR (LA PCR) |
index.php?prt=89 | Protocol 6: Inverse PCR |
index.php?prt=90 | Protocol 7: Nested PCR |
index.php?prt=91 | Protocol 8: Amplification of cDNA Generated by Reverse Transcription of mRNA: Two-Step RT-PCR |
index.php?prt=92 | Protocol 9: Rapid Amplification of Sequences from the 5 Ends of mRNAs: 5-RACE |
index.php?prt=93 | Protocol 10: Rapid Amplification of Sequences from the 3 Ends of mRNAs: 3-RACE |
index.php?prt=94 | Protocol 11: Screening Colonies by PCR |
index.php?prt=95 | Protocol 1: Visualizing Genomic Annotations with the UCSC Genome Browser |
index.php?prt=96 | Protocol 2: Sequence Alignment and Homology Search with BLAST and ClustalW |
index.php?prt=97 | Protocol 3: Designing PCR Primers Using Primer3Plus |
index.php?prt=98 | Protocol 4: Expression Profiling by Microarray and RNA-seq |
index.php?prt=99 | Protocol 5: Mapping Billions of Short Reads to a Reference Genome |
index.php?prt=100 | Protocol 6: Identifying Regions Enriched in a ChIP-seq Data Set (Peak Finding) |
index.php?prt=101 | -Regulatory Motifs |
index.php?prt=102 | Protocol 1: Optimizing Primer and Probe Concentrations for Use in Real-Time PCR |
index.php?prt=103 | Protocol 2: Constructing a Standard Curve |
index.php?prt=104 | Protocol 3: Quantification of DNA by Real-Time PCR |
index.php?prt=105 | Protocol 4: Quantification of RNA by Real-Time RT-PCR |
index.php?prt=106 | Protocol 5: Analysis and Normalization of Real-Time PCR Experimental Data |
index.php?prt=107 | Click here for free access to Chapter 10 in its entirety |
index.php?prt=108 | Protocol 2: Round A/Round B Amplification of DNA |
index.php?prt=109 | Protocol 3: T7 Linear Amplification of DNA (TLAD) for Nucleosomal and Other DNA < 500 bp |
index.php?prt=110 | Protocol 4: Amplification of RNA |
index.php?prt=111 | Protocol 5: Direct Cyanine-dUTP Labeling of RNA |
index.php?prt=112 | Protocol 6: Indirect Aminoallyl-dUTP Labeling of RNA |
index.php?prt=113 | Protocol 7: Cyanine-dCTP Labeling of DNA Using Klenow |
index.php?prt=114 | Protocol 8: Indirect Labeling of DNA |
index.php?prt=115 | Protocol 9: Blocking Polylysines on Homemade Microarrays |
index.php?prt=116 | Protocol 10: Hybridization to Homemade Microarrays |
index.php?prt=117 | Protocol 1: Preparing Plasmid Subclones for Capillary Sequencing |
index.php?prt=118 | Protocol 2: Preparing PCR Products for Capillary Sequencing |
index.php?prt=119 | Protocol 3: Cycle-Sequencing Reactions |
index.php?prt=120 | Protocol 4: Whole Genome: Manual Library Preparation |
index.php?prt=121 | Protocol 5: Whole Genome: Automated, Nonindexed Library Preparation |
index.php?prt=122 | Protocol 6: Whole Genome: Automated, Indexed Library Preparation |
index.php?prt=123 | Protocol 7: Preparation of a 3-kb Mate-Pair Library for Illumina Sequencing |
index.php?prt=124 | Protocol 8: Preparation of an 8-kb Mate-Pair Library for Illumina Sequencing |
index.php?prt=125 | Protocol 9: RNA-Seq: RNA Conversion to cDNA and Amplification |
index.php?prt=126 | Protocol 10: Solution-Phase Exome Capture |
index.php?prt=127 | Protocol 11: Automated Size Selection |
index.php?prt=128 | Protocol 12: Library Quantification Using SYBR Green-qPCR |
index.php?prt=129 | Protocol 13: Library Quantification Using PicoGreen Fluorometry |
index.php?prt=130 | Protocol 14: Library Quantification: Fluorometric Quantitation of Double-Stranded or Single-Stranded DNA Samples Using the Qubit... |
index.php?prt=131 | Protocol 15: Preparation of Small-Fragment Libraries for 454 Sequencing |
index.php?prt=132 | Protocol 16: sstDNA Library Capture and emPCR |
index.php?prt=133 | Protocol 17: Roche/454 Sequencer: Executing a Sequencing Run |
index.php?prt=134 | Protocol 18: Validation |
index.php?prt=135 | Protocol 19: Quality Assessment of Sequence Data |
index.php?prt=136 | Protocol 20: Data Analysis |
index.php?prt=137 | Protocol 1: DNA Bisulfite Sequencing for Single-Nucleotide-Resolution DNA Methylation Detection |
index.php?prt=138 | Protocol 2: Methylation-Specific PCR for Gene-Specific DNA Methylation Detection |
index.php?prt=139 | Protocol 3: Methyl-Cytosine-Based Immunoprecipitation for DNA Methylation Analysis |
index.php?prt=140 | Protocol 4: High-Throughput Deep Sequencing for Mapping Mammalian DNA Methylation |
index.php?prt=141 | Protocol 5: Roche 454 Clonal Sequencing of Bisulfite-Converted DNA Libraries |
index.php?prt=142 | Protocol 6: Illumina Sequencing of Bisulfite-Converted DNA Libraries |
index.php?prt=143 | Protocol 1: Random Priming: Labeling of Purified DNA Fragments by Extension of Random Oligonucleotides |
index.php?prt=144 | Protocol 2: Random Priming: Labeling of DNA by Extension of Random Oligonucleotides in the Presence of Melted Agarose |
index.php?prt=145 | Protocol 3: Labeling of DNA Probes by Nick Translation |
index.php?prt=146 | Protocol 4: Labeling of DNA Probes by Polymerase Chain Reaction |
index.php?prt=147 | Protocol 5: Synthesis of Single-Stranded RNA Probes by In Vitro Transcription |
index.php?prt=148 | Protocol 6: Synthesis of cDNA Probes from mRNA Using Random Oligonucleotide Primers |
index.php?prt=149 | Protocol 7: Radiolabeling of Subtracted cDNA Probes by Random Oligonucleotide Extension |
index.php?prt=150 | DNA Polymerase I |
index.php?prt=151 | Protocol 9: Dephosphorylation of DNA Fragments with Alkaline Phosphatase |
index.php?prt=152 | Protocol 10: Phosphorylation of DNA Molecules with Protruding 5-Hydroxyl Termini |
index.php?prt=153 | Protocol 11: Phosphorylation of DNA Molecules with Dephosphorylated Blunt Ends or Recessed 5 Termini |
index.php?prt=154 | Protocol 12: Phosphorylating the 5 Termini of Oligonucleotides Using T4 Polynucleotide Kinase |
index.php?prt=155 | Protocol 13: Labeling the 3 Termini of Oligonucleotides Using Terminal Deoxynucleotidyl Transferase |
index.php?prt=156 | DNA Polymerase I |
index.php?prt=157 | Protocol 15: Purification of Labeled Oligonucleotides by Precipitation with Ethanol |
index.php?prt=158 | Protocol 16: Purification of Labeled Oligonucleotides by Size-Exclusion Chromatography |
index.php?prt=159 | Column |
index.php?prt=160 | Protocol 18: Hybridization of Oligonucleotide Probes in Aqueous Solutions: Washing in Buffers Containing Quaternary Ammonium Sal... |
index.php?prt=161 | Protocol 1: Random Mutagenesis Using Error-Prone DNA Polymerases |
index.php?prt=162 | Protocol 2: Creating Insertions or Deletions Using Overlap Extension PCR Mutagenesis |
index.php?prt=163 | Protocol 3: In Vitro Mutagenesis Using Double-Stranded DNA Templates: Selection of Mutants with DpnI |
index.php?prt=164 | Protocol 4: Altered -Lactamase Selection Approach for Site-Directed Mutagenesis |
index.php?prt=165 | Protocol 5: Oligonucleotide-Directed Mutagenesis by Elimination of a Unique Restriction Site (USE Mutagenesis) |
index.php?prt=166 | Protocol 6: Saturation Mutagenesis by Codon Cassette Insertion |
index.php?prt=167 | Protocol 7: Random Scanning Mutagenesis |
index.php?prt=168 | Protocol 8: Multisite-Directed Mutagenesis |
index.php?prt=169 | Protocol 9: Megaprimer PCR-Based Mutagenesis |
index.php?prt=170 | Protocol 1: DNA Transfection Mediated by Cationic Lipid Reagents |
index.php?prt=171 | Protocol 2: Calcium-Phosphate-Mediated Transfection of Eukaryotic Cells with Plasmid DNAs |
index.php?prt=172 | Protocol 3: Calcium-Phosphate-Mediated Transfection of Cells with High-Molecular-Weight Genomic DNA |
index.php?prt=173 | Protocol 4: Transfection Mediated by DEAE-Dextran: High-Efficiency Method |
index.php?prt=174 | Protocol 5: DNA Transfection by Electroporation |
index.php?prt=175 | Protocol 6: Analysis of Cell Viability by the alamarBlue Assay |
index.php?prt=176 | Protocol 7: Analysis of Cell Viability by the Lactate Dehydrogenase Assay |
index.php?prt=177 | Protocol 8: Analysis of Cell Viability by the MTT Assay |
index.php?prt=178 | Protocol 1: Construction of Recombinant Adenovirus Genomes by Direct Cloning |
index.php?prt=179 | Protocol 2: Release of the Cloned Recombinant Adenovirus Genome for Rescue and Expansion |
index.php?prt=180 | Protocol 3: Purification of the Recombinant Adenovirus by Cesium Chloride Gradient Centrifugation |
index.php?prt=181 | Protocol 4: Characterization of the Purified Recombinant Adenovirus for Viral Genome Structure by Restriction Enzyme Digestions |
index.php?prt=182 | End-Point Dilution and qPCR |
index.php?prt=183 | Protocol 6: Detection Assay for Replication-Competent Adenovirus by Concentration Passage and Real-Time qPCR |
index.php?prt=184 | Protocol 7: Production of rAAVs by Transient Transfection |
index.php?prt=185 | Protocol 8: Purification of rAAVs by Cesium Chloride Gradient Sedimentation |
index.php?prt=186 | Protocol 9: Purification of rAAVs by Iodixanol Gradient Centrifugation |
index.php?prt=187 | Protocol 10: Purification of rAAV2s by Heparin Column Affinity Chromatography |
index.php?prt=188 | Protocol 11: Enrichment of Fully Packaged Virions in Column-Purified rAAV Preparations by Iodixanol Gradient Centrifugation Foll... |
index.php?prt=189 | Protocol 12: Titration of rAAV Genome Copy Number Using Real-Time qPCR |
index.php?prt=190 | End-Point Dilution and qPCR |
index.php?prt=191 | Protocol 14: Analysis of rAAV Sample Morphology Using Negative Staining and High-Resolution Electron Microscopy |
index.php?prt=192 | Protocol 15: Analysis of rAAV Purity Using Silver-Stained SDS-PAGE |
index.php?prt=193 | Protocol 16: Production of High-Titer Retrovirus and Lentivirus Vectors |
index.php?prt=194 | Protocol 17: Titration of Lentivirus Vectors |
index.php?prt=195 | Protocol 18: Monitoring Lentivirus Vector Stocks for Replication-Competent Viruses |
index.php?prt=196 | Protocol 1: Assay for -Galactosidase in Extracts of Mammalian Cells |
index.php?prt=197 | Protocol 2: Single Luciferase Reporter Assay |
index.php?prt=198 | Protocol 3: Dual Luciferase Reporter Assay |
index.php?prt=199 | Protocol 4: Using ELISA to Measure GFP Production |
index.php?prt=200 | Protocol 5: Generation of Cell Lines with Tetracycline-Regulated Gene Expression |
index.php?prt=201 | Protocol 1: Preparation of siRNA Duplexes |
index.php?prt=202 | Protocol 2: RNAi in Mammalian Cells by siRNA Duplex Transfection |
index.php?prt=203 | S2 Cells by siRNA Duplex Transfection |
index.php?prt=204 | Protocol 4: Preparation of dsRNAs by In Vitro Transcription |
index.php?prt=205 | S2 Cells by dsRNA Soaking |
index.php?prt=206 | S2 Cells by dsRNA Transfection |
index.php?prt=207 | Protocol 7: Analysis of Small RNAs by Northern Hybridization |
index.php?prt=208 | Protocol 8: Analysis of Small RNAs by Quantitative Reverse Transcription PCR |
index.php?prt=209 | Protocol 9: Construction of Small RNA Libraries for High-Throughput Sequencing |
index.php?prt=210 | Protocol 10: Preparation of Antisense Oligonucleotides to Inhibit miRNA Function |
index.php?prt=211 | Protocol 11: Inhibiting miRNA Function by Antisense Oligonucleotides in Cultured Mammalian Cells |
index.php?prt=212 | S2 Cells |
index.php?prt=213 | Using IPTG-Inducible Promoters |
index.php?prt=214 | Protocol 2: Expression of Cloned Genes Using the Baculovirus Expression System |
index.php?prt=215 | Using the Methanol-Inducible Promoter AOX1 |
index.php?prt=216 | Protocol 4: Preparation of Cell Extract for Purification of Soluble Proteins Expressed in E. coli |
index.php?prt=217 | Protocol 5: Purification of Polyhistidine-Tagged Proteins by Immobilized Metal Affinity Chromatography |
index.php?prt=218 | Protocol 6: Purification of Fusion Proteins by Affinity Chromatography on Glutathione Resin |
index.php?prt=219 | Protocol 7: Solubilization of Expressed Proteins from Inclusion Bodies |
index.php?prt=220 | Protocol 8: SDS-PAGE of Proteins |
index.php?prt=221 | Protocol 9: Analysis of Proteins by Immunoblotting |
index.php?prt=222 | Protocol 10: Methods for Measuring the Concentrations of Proteins |
index.php?prt=223 | Protocol 1: Formaldehyde Cross-Linking |
index.php?prt=224 | Protocol 2: Preparation of Cross-Linked Chromatin for ChIP |
index.php?prt=225 | Protocol 3: ChIP |
index.php?prt=226 | Protocol 4: ChIPQuantitative PCR (ChIP-qPCR) |
index.php?prt=227 | Protocol 5: ChIP-chip |
index.php?prt=228 | Protocol 6: ChIP-seq |
index.php?prt=229 | Protocol 7: Generation of 3C Libraries from Cross-Linked Cells |
index.php?prt=230 | Protocol 8: Generation of ChIP-loop Libraries |
index.php?prt=231 | Protocol 9: Generation of Control Ligation Product Libraries |
index.php?prt=232 | Protocol 10: PCR Detection of 3C Ligation Products Present in 3C, ChIP-loop, and Control Libraries: Library Titration and Intera... |
index.php?prt=233 | Protocol 11: 4C Analysis of 3C, ChIP-loop, and Control Libraries |
index.php?prt=234 | Protocol 12: 5C Analysis of 3C, ChIP-loop, and Control Libraries |
index.php?prt=235 | Protocol 1: Optimization of Immunoprecipitation Stringency for CLIP |
index.php?prt=236 | Protocol 2: UV Cross-Linking of Live Cells and Lysate Preparation |
index.php?prt=237 | Protocol 3: RNase Titration, Immunoprecipitation, and SDS-PAGE |
index.php?prt=238 | Protocol 4: 3-Linker Ligation and Size Selection by SDS-PAGE |
index.php?prt=239 | Protocol 5: Isolation of the RNA Tags, 5-Linker Ligation, and Reverse Transcription PCR Amplification |
index.php?prt=240 | Protocol 6: Sequencing of RNA CLIP Tags |
index.php?prt=241 | Protocol 7: Gel Purification and Storage of RNA Linkers |
index.php?prt=242 | Protocol 1: Generating Yeast One-Hybrid DNA-Bait Strains |
index.php?prt=243 | Protocol 2: Generating Yeast Two-Hybrid Bait Strains |
index.php?prt=244 | Protocol 3: Identifying Interactors from an Activation Domain Prey Library |
index.php?prt=245 | Protocol 4: High-Efficiency Yeast Transformation |
index.php?prt=246 | Protocol 5: Colony Lift Colorimetric Assay for -Galactosidase Activity |
index.php?prt=247 | Protocol 6: Yeast Colony PCR |
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Name Server: PHAGE.CSHL.ORG
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of whois database: 2018-10-19T14:45:28Z <<<
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currently set to expire. This date does not necessarily reflect the expiration
date of the domain name registrant's agreement with the sponsoring
registrar. Users may consult the sponsoring registrar's Whois database to
view the registrar's reported date of expiration for this registration.
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reserves the right to modify these terms at any time.
The Registry database contains ONLY .COM, .NET, .EDU domains and
Registrars.
ФРГ - Деттинген-унтер-Тек - 176.9.118.138
ФРГ - Деттинген-унтер-Тек - 176.9.118.139
Нидерланды - Амстердам - 85.17.177.246
Hetzner Online GmbH
LeaseWeb
Hetzner Online GmbH
LeaseWeb B.V.
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