Direct radioactive labeling of unpurified PCR products using Klenow fragment.

Abstract:

:We describe a method for rapid radioactive labeling of PCR product. The method, employing the Klenow fragment of DNA polymerase I, consumes little product, requires no product purification and takes under 30 minutes.

journal_name

Biotechniques

journal_title

BioTechniques

authors

McDaniel TK,Huang Y,Yin J,Needleman SW,Meltzer SJ

subject

Has Abstract

pub_date

1991-08-01 00:00:00

pages

164, 166

issue

2

eissn

0736-6205

issn

1940-9818

journal_volume

11

pub_type

杂志文章
  • Construction of a bicistronic vector for the co-expression of two genes in Caenorhabditis elegans using a newly identified IRES.

    abstract::The nematode Caenorhabditis elegans is an important model animal for biological research. Currently, transgenic C. elegans strains are mainly generated by injecting DNA encoding a gene of interest, in combination with a reporter gene, into the gonad. With this approach, the interpretation of negative results, such as ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113821

    authors: Li D,Wang M

    更新日期:2012-03-01 00:00:00

  • PABS: an online platform to assist BAC-by-BAC sequencing projects.

    abstract::Genome sequencing projects are either based on whole genome shotgun (WGS) or on a BAC-by-BAC strategy. Although WGS is in most cases the preferred choice, sometimes the BAC-by-BAC approach may be better because it requires a much simpler assembly process. Furthermore, when the study is limited to specific regions of t...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112686

    authors: Todesco S,Campagna D,Levorin F,D'Angelo M,Schiavon R,Valle G,Vezzi A

    更新日期:2008-01-01 00:00:00

  • Real-time measurement of PMA-induced cellular alterations by microelectrode array-based impedance spectroscopy.

    abstract::For a feasible and cost-effective impedance measurement of cellular alterations in real-time, we combined commercially available microelectrode arrays (MEAs), consisting of 60 microelectrodes, with a conventional impedance analyzer. For proof of principle, a breast carcinoma cell line (MCF-7) was cultured on MEAs, and...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112254

    authors: Rothermel A,Nieber M,Müller J,Wolf P,Schmidt M,Robitzki AA

    更新日期:2006-10-01 00:00:00

  • Quantitative measurement of proteins by western blotting with Cy5-coupled secondary antibodies.

    abstract::The concentration of proteins in cells is an important parameter that determines how a protein will interact with other proteins or pharmacological agents. Recent developments in Western blotting techniques have now made this a method of choice to measure protein concentration in complex solutions such as total cell e...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Fradelizi J,Friederich E,Beckerle MC,Golsteyn RM

    更新日期:1999-03-01 00:00:00

  • Pulse-first heterofusion of cells by electric field pulses and associated loading of macromolecules into mammalian cells.

    abstract::Exposing cells to brief, high-intensity electrical field pulses can lead to the permeabilization of their plasma membranes. This electro-induced permeated state of the cell membrane is reversible and leads to cell fusion; i.e., the electropermeabilized state if fusogenic. The size of cells intended for fusing, however...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Rols MP,Dahhou F,Teissié J

    更新日期:1994-10-01 00:00:00

  • Improved extraction of PCR-quality community DNA from digesta and fecal samples.

    abstract::Several DNA extraction methods have been reported for use with digesta or fecal samples, but problems are often encountered in terms of relatively low DNA yields and/or recovering DNA free of inhibitory substances. Here we report a modified method to extract PCR-quality microbial community DNA from these types of samp...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/04365ST04

    authors: Yu Z,Morrison M

    更新日期:2004-05-01 00:00:00

  • Effective flow cytometric phenotyping of cells using minimal amounts of antibody.

    abstract::Here we introduce a modified antibody staining method that uses up to 80% less antibody for flow cytometry. We demonstrate this method for the detection of antigens expressed at high, moderate, or low levels in mouse and rat lymphocytes as well as mouse mammary epithelial cells. We obtained reproducibly accurate resul...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/0000113854

    authors: Sharma D,Eichelberg MR,Haag JD,Meilahn AL,Muelbl MJ,Schell K,Smits BM,Gould MN

    更新日期:2012-07-01 00:00:00

  • Determination of human NAT2 acetylator genotype by oligonucleotide ligation assay.

    abstract::The oligonucleotide ligation assay (OLA) was adapted to the genotyping of the N-arylamine-acetyltransferase (NAT2) gene. This assay allows the use of 96-well microplates and robotic workstations for high sample throughput. We found this assay to be accurate, efficient and reliable. Another advantage for epidemiologica...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/97224st03

    authors: Bigler J,Chen C,Potter JD

    更新日期:1997-04-01 00:00:00

  • A simple method for isolation of DNA from blood clots suited for use in PCR.

    abstract::We describe a rapid, simple and inexpensive method for the isolation of DNA from blood clots suited for use in PCR. Our method is based on the lysing and nuclease-inactivating properties of guanidine thiocyanate together with the nucleic acid-binding properties of silica particles. Isolated DNA can be used for in vitr...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Zeillinger R,Schneeberger C,Speiser P,Kury F

    更新日期:1993-02-01 00:00:00

  • Continuous fluorescence monitoring of rapid cycle DNA amplification.

    abstract::Rapid cycle DNA amplification was continuously monitored by three different fluorescence techniques. Fluorescence was monitored by (i) the double-strand-specific dye SYBR Green I, (ii) a decrease in fluorescein quenching by rhodamine after exonuclease cleavage of a dual-labeled hydrolysis probe and (iii) resonance ene...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/97221bi01

    authors: Wittwer CT,Herrmann MG,Moss AA,Rasmussen RP

    更新日期:1997-01-01 00:00:00

  • Maleimide scavenging enhances determination of protein S-palmitoylation state in acyl-exchange methods.

    abstract::S-palmitoylation (S-acylation) is emerging as an important dynamic post-translational modification of cysteine residues within proteins. Current assays for protein S-palmitoylation involve either in vivo labeling or chemical cleavage of S-palmitoyl groups to reveal a free cysteine sulfhydryl that can be subsequently l...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114516

    authors: Hurst CH,Turnbull D,Plain F,Fuller W,Hemsley PA

    更新日期:2017-02-01 00:00:00

  • Generation of clonal DNA templates for in vitro transcription without plasmid purification.

    abstract::WE present a rapid procedure based on the polymerase chain reaction for generation of double-stranded DNA templates suitable for in vitro transcription by T3 or T7 RNA polymerase. DNA fragments cloned into a phage promoter vector are amplified together with a flanking promoter to provide functional templates. Extensio...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Weier HU,Rosette C

    更新日期:1990-03-01 00:00:00

  • Enhanced detection of beta-galactosidase reporter activation is achieved by a reduction of hemoglobin content in tissue lysates.

    abstract::beta-galactosidase (beta-gal), the product of the E. coli LacZ gene, has been used extensively as a reporter in numerous systems. Until recently, the most commonly used method of detecting beta-gal reporter enzymatic activity was a colormetric assay based on the cleavage of the beta-gal substrate 5-bromo-4-chloro-3-in...

    journal_title:BioTechniques

    pub_type:

    doi:10.2144/01304st03

    authors: Nazarenko DA,Dertinger SD,Gasiewicz TA

    更新日期:2001-04-01 00:00:00

  • Amplification of reproducible allele markers for amplified fragment length polymorphism analysis.

    abstract::A procedure for amplification by PCR of reproducible allele markers for amplified fragment length polymorphism (Amp-FLP) analysis is presented. We have prepared markers for the allelic products of the VNTR loci D1S80 (MCT118) and D17S30 (YNZ22) and for the hypervariable VNTR locus close to the 3' end of the apolipopro...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Sajantila A,Puomilahti S,Johnsson V,Ehnholm C

    更新日期:1992-01-01 00:00:00

  • Bacterial IMPDH gene used for the selection of mammalian cell transfectants.

    abstract::Stable cell transfection is used for the expression of exogenous genes or cDNAs in eukaryotic cells. Selection of these transfectants requires a dominant selectable marker. A variety of such markers has been identified and is currently in use. However, many of these are not suitable for all cell types or require uniqu...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/03346st05

    authors: Baccam M,Huberman E

    更新日期:2003-06-01 00:00:00

  • Measurement of isolated myocyte volume using the Coulter models Z2 and ZM/C256: a comparison of instrument function.

    abstract::Changes in cardiac structure that depart from normal have generally been termed "remodeling". Assessment of ventricular remodeling at the cellular level should include measurement of myocyte dimensions. A well-established and reliable method to assess myocyte remodeling uses isolated cells and the Coulter Counter/Chan...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/98253pf02

    authors: Said S,Tamura T,Gerdes AM

    更新日期:1998-09-01 00:00:00

  • Rapid polymerase chain reaction amplification using intact bacterial cells.

    abstract::We have demonstrated that efficient polymerase chain reaction amplifications from chromosomal DNA can be carried out using whole bacterial cells as the starting material. Cells from the liquid or solid cultures can be used directly, without any pre-treatment, thus eliminating the need for DNA isolation. ...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Joshi AK,Baichwal V,Ames GF

    更新日期:1991-01-01 00:00:00

  • AMDA 2.13: A major update for automated cross-platform microarray data analysis.

    abstract::Microarray platforms require analytical pipelines with modules for data pre-processing including data normalization, statistical analysis for identification of differentially expressed genes, cluster analysis, and functional annotation. We previously developed the Automated Microarray Data Analysis (AMDA, version 2.3....

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/0000113889

    authors: Kapetis D,Clarelli F,Vitulli F,de Rosbo NK,Beretta O,Foti M,Ricciardi-Castagnoli P,Zolezzi F

    更新日期:2012-07-01 00:00:00

  • Self-seal reagent: evaporation control for molecular histology procedures without chambers, clips or fingernail polish.

    abstract::Sensitive nucleic acid based detection methods such as in situ PCR, in situ RT-PCR and PRINS have great potential in the areas of developmental biology, pathogenesis and diagnostics. However, control of evaporation from in situ reactions is critical to ensure reliable data. Self-Seal Reagent, a component added directl...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/97232pf01

    authors: Sullivan DE,Bobroski LE,Bagasra O,Finney M

    更新日期:1997-08-01 00:00:00

  • Generation and characterization of recombinant vascular targeting agents from hybridoma cell lines.

    abstract::Vascular targeting agents (VTAs) can be produced by linking antibodies or antibody fragments directed against endothelial cell markers to effector moieties. So far, it has been necessary to produce the components of VTAs (antibody, antibody fragment, linker, and effector) separately and, subsequently, to conjugate the...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/01301dd03

    authors: Gottstein C,Wels W,Ober B,Thorpe PE

    更新日期:2001-01-01 00:00:00

  • CDNA library construction from a small amount of RNA: adaptor-ligation approach for two-round cRNA amplification using T7 and SP6 RNA polymerases.

    abstract::In this study, we developed a method that allows cDNA library construction from a small amount of RNA without causing serious size bias in the resulting cDNA population. For this purpose, we adopted two-round cRNA amplification by T7 and SP6 RNA polymerases. The first-round cDNAs, flanked by the promoter sequences of ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/05383RR01

    authors: Ohara R,Kikuno RF,Kitamura H,Ohara O

    更新日期:2005-03-01 00:00:00

  • Microsatellite marker discovery using single molecule real-time circular consensus sequencing on the Pacific Biosciences RS.

    abstract::Microsatellite sequences are important markers for population genetics studies. In the past, the development of adequate microsatellite primers has been cumbersome. However with the advent of next-generation sequencing technologies, marker identification in genomes of non-model species has been greatly simplified. Her...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114104

    authors: Grohme MA,Soler RF,Wink M,Frohme M

    更新日期:2013-11-01 00:00:00

  • Improved recombinant retroviral titers utilizing trichostatin A.

    abstract::Recombinant retroviruses are a common vehicle to deliver an exogenous gene to a target cell, which makes them a useful tool in the field of gene therapy. A major drawback to using recombinant retroviruses is the low titer achieved, resulting in a limited number of target cells infected and subsequently poor expression...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/00294rr05

    authors: Tobias CA,Kim D,Fischer I

    更新日期:2000-10-01 00:00:00

  • Transient dominant host-range selection using Chinese hamster ovary cells to generate marker-free recombinant viral vectors from vaccinia virus.

    abstract::Recombinant vaccinia viruses (rVACVs) are promising antigen-delivery systems for vaccine development that are also useful as research tools. Two common methods for selection during construction of rVACV clones are (i) co-insertion of drug resistance or reporter protein genes, which requires the use of additional selec...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114537

    authors: Liu L,Cooper T,Eldi P,Garcia-Valtanen P,Diener KR,Howley PM,Hayball JD

    更新日期:2017-04-01 00:00:00

  • Detection and molecular mass determination of an HIV replication-enhancing female genital tract factor using a blot bioassay.

    abstract::We previously reported that cervicovaginal lavages (CVL) contain a factor that enhances the replication of human immunodeficiency virus (HIV) by increasing virus transcription in T cells and monocytoid cells. This factor was named the HIV-inducing factor (HIF). To determine the molecular mass of HIF, we adapted a blot...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/00283st05

    authors: Hashemi FB,Spear GT,Madsen L,Mollenhauer J

    更新日期:2000-03-01 00:00:00

  • A novel vector for positive selection of inserts harboring an open reading frame by translational coupling.

    abstract::We have developed a novel vector pTCS, as a tool for efficient selection of open reading frame (ORF)-containing inserts. In pTCS clones containing an insert with an ORF a downstream marker gene (immE3, conferring resistance to colicin) is activated via translational coupling with the insert, and transformed cells can ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112629

    authors: Ohashi-Kunihiro S,Yohda M,Masaki H,Machida M

    更新日期:2007-12-01 00:00:00

  • Colorimetric detection of loop-mediated isothermal amplification reaction by using hydroxy naphthol blue.

    abstract::Loop-mediated isothermal amplification (LAMP), a novel gene amplification method, enables the synthesis of larger amounts of both DNA and a visible byproduct--namely, magnesium pyrophosphate--without thermal cycling. A positive reaction is indicated by the turbidity of the reaction solution or the color change after a...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113072

    authors: Goto M,Honda E,Ogura A,Nomoto A,Hanaki K

    更新日期:2009-03-01 00:00:00

  • A method for visualizing fluorescence of flavonoid therapeutics in vivo in the model eukaryote Dictyostelium discoideum.

    abstract::Naturstoff reagent A (diphenylboric acid 2-aminoethyl ester [DPBA]) has been used historically in plant science to observe polyphenolic pigments, such as flavonoids, whose fluorescence requires enhancement to be visible by microscopy. Flavonoids are common dietary constituents and are the focus of considerable attenti...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/btn-2018-0084

    authors: Ferrara BT,Thompson EP

    更新日期:2019-02-01 00:00:00

  • Improving the limit of detection for Sanger sequencing: a comparison of methodologies for KRAS variant detection.

    abstract::Fluorescent dye terminator Sanger sequencing (FTSS), with detection by automated capillary electrophoresis (CE), has long been regarded as the gold standard for variant detection. However, software analysis and base-calling algorithms used to detect mutations were largely optimized for resequencing applications in whi...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113913

    authors: Davidson CJ,Zeringer E,Champion KJ,Gauthier MP,Wang F,Boonyaratanakornkit J,Jones JR,Schreiber E

    更新日期:2012-09-01 00:00:00

  • A simple microfluidic device for live cell imaging of Arabidopsis cotyledons, leaves, and seedlings.

    abstract::One of the challenges of performing live-cell imaging in plants is establishing a system for securing the sample during imaging that allows for the rapid addition of treatments. Here we report how a commercially available device called a HybriWell™ can be repurposed to create an imaging chamber suitable for Arabidopsi...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/btn-2018-0044

    authors: Vang S,Seitz K,Krysan PJ

    更新日期:2018-06-01 00:00:00