Template secondary structure promotes polymerase jumping during PCR amplification.

Abstract:

:Pairs of primers flanking known miniTn10 transposon insertion sites were used to confirm the presence of the transposon in DNA isolated from Legionella pneumophila mutants. It was expected that the polymerase chain reaction products derived from the mutant template would be larger than those from the wild-type (WT) template due to the presence of the 1.8-kb transposon. Instead, it was observed that the mutant template yielded a product of almost the same size as that yielded by WT template. We present evidence to indicate that the aberrant product from the mutant template is a direct result of secondary structure of the template resulting from an inverted repeat sequence present in the miniTn10 transposon.

journal_name

Biotechniques

journal_title

BioTechniques

authors

Viswanathan VK,Krcmarik K,Cianciotto NP

doi

10.2144/99273st04

subject

Has Abstract

pub_date

1999-09-01 00:00:00

pages

508-11

issue

3

eissn

0736-6205

issn

1940-9818

journal_volume

27

pub_type

  • Copper treatment increases recombinant baculovirus production and polyhedrin and p10 expression.

    abstract::Treatment with 2 mM CuSO4 was used to induce a Drosophila melanogaster metallothionein (Mtn) promoter that had been cloned into a recombinant baculovirus. Careful study revealed that the Mtn promoter functioned as an inducible, if somewhat "leaky" promoter within the context of baculovirus-infected cells. In the proce...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/97234rr01

    authors: Lanier LM,Storm K,Shafaie A,Volkman LE

    更新日期:1997-10-01 00:00:00

  • A rapid and reliable method to create tandem arrays of short DNA sequences.

    abstract::Tandemly polymerized regulatory elements, antisense RNA segments or ribozymes are potentially useful in selective gene silencing. However, existing methods of tandemly polymerizing short DNA segments are laborious. We present a procedure that can create cloned arrays of 40-70 monomer units in two steps. We have create...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Graham GJ,Maio JJ

    更新日期:1992-11-01 00:00:00

  • Protein aggregation mediated by cysteine oxidation during the stacking phase of discontinuous buffer SDS-PAGE.

    abstract::The resolution of complex protein mixtures by discontinuous buffer SDS-PAGE is accomplished by their concentration into thin bands in the stacking gel, followed by their separation during migration through the resolving gel. Recombinant human interferon-inducible protein-10 (IP-10), a 10-kDa C-X-C chemokine with four ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/01302st04

    authors: Crow MK,Karasavvas N,Sarris AH

    更新日期:2001-02-01 00:00:00

  • Solid-phase gene assembly of constructs derived from the Plasmodium falciparum malaria blood-stage antigen Ag332.

    abstract::A general method for solid-phase gene assembly on streptavidin-coated magnetic beads has been developed. The introduction of biotin in the 5'-end of the initiation oligonucleotide enables anchoring to the bead by means of the streptavidin-biotin interaction. The immobilization of one oligonucleotide enables controlled...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Ståhl S,Hansson M,Ahlborg N,Nguyen TN,Liljeqvist S,Lundeberg J,Uhlén M

    更新日期:1993-03-01 00:00:00

  • Efficient and robust preparation of tyrosine phosphorylated intrinsically disordered proteins.

    abstract::Intrinsically disordered proteins (IDPs) are subject to post-translational modifications. This allows the same polypeptide to be involved in different interaction networks with different consequences, ranging from regulatory signalling networks to the formation of membrane-less organelles. We report a robust method fo...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/btn-2019-0033

    authors: Brázda P,Šedo O,Kubíček K,Štefl R

    更新日期:2019-07-01 00:00:00

  • Simplified DGS procedure for large-scale genome structural study.

    abstract::Ditag genome scanning (DGS) uses next-generation DNA sequencing to sequence the ends of ditag fragments produced by restriction enzymes. These sequences are compared to known genome sequences to determine their structure. In order to use DGS for large-scale genome structural studies, we have substantially revised the ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113294

    authors: Jung YC,Xu J,Chen J,Kim Y,Winchester D,Wang SM

    更新日期:2009-11-01 00:00:00

  • Cautionary note on the use of Caenorhabditis elegans to study muscle phenotypes caused by mutations in the human MYH7 gene.

    abstract::Mutations in the human MYH7 gene, encoding a slow skeletal muscle/β-cardiac myosin heavy chain, cause different types of myopathies. The nematode model Caenorhabditis elegans has frequently been employed to study the molecular and physiological consequences of MYH7 mutations in muscle function by introducing mutations...

    journal_title:BioTechniques

    pub_type: 信件

    doi:10.2144/btn-2020-0012

    authors: Gil-Gálvez A,Carbonell-Corvillo P,Paradas C,Miranda-Vizuete A

    更新日期:2020-06-01 00:00:00

  • Antibody-mediated soluble CD14 stabilization prevents agitation-induced increases in presepsin levels in blood component specimens.

    abstract::Presepsin is a 13-kDa N-terminal glycoprotein of CD14. Previously, agitation-induced increases in presepsin levels have been reported; however, the mechanism remains poorly understood. In this study, we aimed to reveal the mechanism of presepsin increase. The agitated plasma or serum was separated using gel exclusion ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/btn-2020-0136

    authors: Morino G,Takahashi G,Kan S,Inoue Y,Sato K,Shirakawa K

    更新日期:2021-01-29 00:00:00

  • Chemically-induced affinity star restriction specificity: a novel TspGWI/sinefungin endonuclease with theoretical 3-bp cleavage frequency.

    abstract::The type IIS/IIC restriction endonuclease TspGWI recognizes the sequence 5'-ACGGA-3', cleaving DNA 11/9 nucleotides downstream. Here we show that sinefungin, a cofactor analog of S-adenosyl methionine, induces a unique type of relaxation in DNA recognition specificity. In the presence of sinefungin, TspGWI recognizes ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113685

    authors: Zylicz-Stachula A,Zołnierkiewicz O,Jeżewska-Frąckowiak J,Skowron PM

    更新日期:2011-06-01 00:00:00

  • Staining and embedding of human chromosomes for 3-d serial block-face scanning electron microscopy.

    abstract::The high-order structure of human chromosomes is an important biological question that is still under investigation. Studies have been done on imaging human mitotic chromosomes using mostly 2-D microscopy methods. To image micron-sized human chromosomes in 3-D, we developed a procedure for preparing samples for serial...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114236

    authors: Yusuf M,Chen B,Hashimoto T,Estandarte AK,Thompson G,Robinson I

    更新日期:2014-12-01 00:00:00

  • Characterizing the spatio-temporal behavior of cell populations through image auto- and cross-correlation microscopy.

    abstract::We propose two methods for characterizing the spatio-temporal behavior of cell populations in culture. The first method, image auto-correlation microscopy (IACM), allows us to characterize the variation in the number of objects as a function of time, thus enabling the quantification of the clustering properties of cel...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112478

    authors: Bonnet N,Delavoie F,Zahm JM

    更新日期:2007-07-01 00:00:00

  • Automation of dideoxynucleotide DNA sequencing reactions using a robotic workstation.

    abstract::We report here a system for automation of the dideoxynucleotide DNA sequencing method. The system consists of a Beckman Biomek 1000 robotic workstation which has been modified by the addition of a thin heater/cooler block directly on the instrument table. The heater/cooler block, which is regulated by a user-specified...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Wilson RK,Yuen AS,Clark SM,Spence C,Arakelian P,Hood LE

    更新日期:1988-09-01 00:00:00

  • Rapid high resolution western blotting: from gel to image in a single day.

    abstract::A streamlined protocol is described that allows high sensitivity antigen detection by Western blotting in a single day. The choice of membrane blotting matrix, as well as blocking reagents, has been optimized in order to allow rapid development of the blot with chemiluminescent reagents. The entire process, from gel t...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Klapper A,MacKay B,Resh MD

    更新日期:1992-05-01 00:00:00

  • Gene identification by arrested primer extension.

    abstract::This paper reports a novel method for the identification of nucleic acid target sequences when these targets have high sequence identity. Homologous genes are currently identified by sequencing. We hypothesize that by primer extension in the presence of selected nucleotides, genes with similar sequence can be identifi...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Sandhu GS,Kline BC,Bolander ME,Sarkar G

    更新日期:1993-06-01 00:00:00

  • Genetically encoded far-red fluorescent sensors for caspase-3 activity.

    abstract::Caspase-3 is a key effector caspase that is activated in both extrinsic and intrinsic pathways of apoptosis. Available fluorescent sensors for caspase-3 activity operate in relatively short wavelength regions and are nonoptimal for multiparameter microscopy and whole-body imaging. In the present work, we developed new...

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    pub_type: 杂志文章

    doi:10.2144/000114377

    authors: Zlobovskaya OA,Sergeeva TF,Shirmanova MV,Dudenkova VV,Sharonov GV,Zagaynova EV,Lukyanov KA

    更新日期:2016-02-01 00:00:00

  • A streamlined ribosome profiling protocol for the characterization of microorganisms.

    abstract::Ribosome profiling is a powerful tool for characterizing in vivo protein translation at the genome scale, with multiple applications ranging from detailed molecular mechanisms to systems-level predictive modeling. Though highly effective, this intricate technique has yet to become widely used in the microbial research...

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    pub_type: 杂志文章

    doi:10.2144/000114302

    authors: Latif H,Szubin R,Tan J,Brunk E,Lechner A,Zengler K,Palsson BO

    更新日期:2015-06-01 00:00:00

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    abstract::Phage display holds a key position in the use of combinatorial library approaches for the purpose of protein engineering and discovery. However, modifying the pIII protein of the phage can severely and negatively influence the infectiousness of the phage particle. This concern is particularly relevant when large pIII ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112724

    authors: Løset GÅ,Kristinsson SG,Sandlie I

    更新日期:2008-04-01 00:00:00

  • An inexpensive and simple method for thermally stable immobilization of DNA on an unmodified glass surface: UV linking of poly(T)10-poly(C)10-tagged DNA probes.

    abstract::Microarrays printed on glass slides are often constructed by covalently linking modified oligonucleotide probes to a derivatized surface at considerable expense. In this article, we demonstrate that 14-base oligonucleotides with a poly(T)10 - poly(C)10 tail (TC tag), but otherwise unmodified, can be linked by UV light...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112905

    authors: Gudnason H,Dufva M,Duong Bang D,Wolff A

    更新日期:2008-09-01 00:00:00

  • Optimized protocol for linear RNA amplification and application to gene expression profiling of human renal biopsies.

    abstract::Gene expression analysis using high-density cDNA or oligonucleotide arrays is a rapidly emerging tool for transcriptomics, the analysis of the transcriptional state of a cell or organ. One of the limitations of current methodologies is the requirement of a relatively large amount of total or polyadenylated RNA as star...

    journal_title:BioTechniques

    pub_type: 杂志文章

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    authors: Scherer A,Krause A,Walker JR,Sutton SE,Serón D,Raulf F,Cooke MP

    更新日期:2003-03-01 00:00:00

  • Improved accuracy in direct automated DNA sequencing of small PCR products by optimizing the template concentration.

    abstract::Data are presented illustrating the optimum concentration range of reverse transcription PCR-generated products under 500 bp for accurate base calling with direct automated DNA sequencing. A 357-bp fragment of the human estrogen receptor, which includes the DNA binding domain of the protein, was used as a representati...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Hyder SM,Hu C,Needleman DS,Sonoda Y,Wang XY,Baker VV

    更新日期:1994-09-01 00:00:00

  • Nonradioactive assay for sequence-specific DNA binding proteins.

    abstract::A nonradioactive functional assay was developed to quantitate DNA binding proteins. The assay was designed to allow the use of 96-well microplates for high sample throughput. We show that the assay can measure sequence-specific DNA binding of purified proteins as well as DNA binding activity present in whole cell extr...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Gubler ML,Abarzúa P

    更新日期:1995-06-01 00:00:00

  • Paradoxical effect of eukaryotic expression vectors on reporters.

    abstract::A critical issue in transfection or co-transfection experiments is to define the appropriate controls. In most cases, a corresponding empty vector is used as one control. We report a paradoxical effect of empty mammalian expression vectors on different reporters. We have found that different empty vectors can inhibit ...

    journal_title:BioTechniques

    pub_type:

    doi:10.2144/02331st04

    authors: Hu Q,Suzuki K,Hirschler-Laszkiewicz I,Rothblum LI

    更新日期:2002-07-01 00:00:00

  • Limitations for purification of murine interleukin-18 when expressed as a fusion protein containing the FLAG peptide.

    abstract::As a strategy to purify recombinant murine Interleukin (IL)-18, we cloned the mature coding region of this protein into the pFLAG-1 expression system. The intent was to use the FLAG peptide "tag" as an amino terminal addition to IL-18 so that purification of this fusion protein (FLAG-IL-18) on anti-FLAG antibody affin...

    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Elhofy A,Bost KL

    更新日期:1998-09-01 00:00:00

  • Reduced serum methods for contact-based coculture of human dermal fibroblasts and epidermal keratinocytes.

    abstract::Direct contact-based coculture of human dermal fibroblasts and epidermal keratinocytes has been a long-standing and challenging issue owing to different serum and growth factor requirements of the two cell types. Existing protocols employ high serum concentrations (up to 10% fetal bovine serum), complex feeder systems...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/btn-2020-0112

    authors: Kadam S,Vandana M,Kaushik KS

    更新日期:2020-11-01 00:00:00

  • Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing.

    abstract::Sequence-based methods for transcriptome characterization have typically relied on generation of either serial analysis of gene expression tags or expressed sequence tags. Although such approaches have the potential to enumerate transcripts by counting sequence tags derived from them, they typically do not robustly su...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112900

    authors: Morin R,Bainbridge M,Fejes A,Hirst M,Krzywinski M,Pugh T,McDonald H,Varhol R,Jones S,Marra M

    更新日期:2008-07-01 00:00:00

  • Microdissection of spatially identified single nuclei in a solid tumor for single cell whole genome sequencing.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113860

    authors: Guo Y,Yang Y,Zhou J,Czajkowsky DM,Liu B,Shao Z

    更新日期:2012-04-01 00:00:00

  • Reproducibility in the quantification of mRNA levels by RT-PCR-ELISA and RT competitive-PCR-ELISA.

    abstract::The use of reverse transcription (RT) PCR for relative quantitation of gene transcripts relies on the reproducibility of the individual RT, PCR and product measurement steps. Semi-competitive RT-PCR (RT-cPCR) uses an internal competitor template in the PCR step to improve quantitation. We have surveyed the reproducibi...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/98244rr02

    authors: Hall LL,Bicknell GR,Primrose L,Pringle JH,Shaw JA,Furness PN

    更新日期:1998-04-01 00:00:00

  • In situ hybridization with digoxigenin-labeled DNA of human papillomaviruses (HPV 16/18) in HeLa and SiHa cells.

    abstract::To establish a nonradioactive method for demonstrating HPV DNA in routinely treated smears of the uterine cervix (alcohol fixation, staining according to Papanicolaou, preservation), in situ hybridizations were carried out in HeLa and SiHa cells grown on slides. After detailed investigations, the sensitivity and speci...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Heiles HB,Genersch E,Kessler C,Neumann R,Eggers HJ

    更新日期:1988-11-01 00:00:00

  • Chemiluminescent substrates increase sensitivity of antigen detection in western blots.

    abstract::Replacement of colorimetric substrates in Western blots by chemiluminescent reagents enhances the sensitivity of detection by more than an order of magnitude. Protein levels beyond the detection limit of colorimetric substrates can be consistently detected without modifying pre-existing laboratory protocols. ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Sandhu GS,Eckloff BW,Kline BC

    更新日期:1991-07-01 00:00:00

  • [Letter to the Editor] Many commercial hot-start polymerases demonstrate activity prior to thermal activation.

    abstract::Address correspondence to Martin A. Kennedy, Department of Pathology & Carney Centre for Pharmacogenomics, University of Otago, Christchurch, PO Box 4345, Christchurch, New Zealand. E-mail: martin.kennedy@otago.ac.nz. ...

    journal_title:BioTechniques

    pub_type: 信件

    doi:10.2144/000114481

    authors: Stevens AJ,Appleby S,Kennedy MA

    更新日期:2016-12-01 00:00:00