Bifunctional protein conferring enhanced green fluorescence and puromycin resistance.

Abstract:

:A new genetic marker was created in which sequences from enhanced green fluorescent protein were fused to those of puromycin N-acetyl transferase. The resulting fusion protein (EGFP-puro) conferred both green fluorescence and resistance to puromycin when expressed in mammalian cells. The utility of EGFP-puro as a selectable/screenable marker was demonstrated by the ease with which a recombinant guinea pig cytomegalovirus containing EGFP-puro was isolated by a combination of puromycin selection and screening for green fluorescence. We conclude that EGFP-puro is a compact and versatile marker that should prove useful for recombinant virus and transgenic cell line construction, particularly in applications in which coding capacity is limited.

journal_name

Biotechniques

journal_title

BioTechniques

authors

Abbate J,Lacayo JC,Prichard M,Pari G,McVoy MA

doi

10.2144/01312st05

subject

Has Abstract

pub_date

2001-08-01 00:00:00

pages

336-40

issue

2

eissn

0736-6205

issn

1940-9818

journal_volume

31

pub_type

  • Template secondary structure promotes polymerase jumping during PCR amplification.

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    journal_title:BioTechniques

    pub_type:

    doi:10.2144/99273st04

    authors: Viswanathan VK,Krcmarik K,Cianciotto NP

    更新日期:1999-09-01 00:00:00

  • Pyrophosphorolysis-activated polymerization (PAP): application to allele-specific amplification.

    abstract::To measure mutation load or to detect minimal residual disease, a robust method for identifying one mutant allele in the range of 10(6)-10(9) wild-type alleles would be advantageous. Herein, we present evidence that pyrophosphorolysis-activated polymerization (PAP) has the potential to provide a highly specific and ro...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/00295rr03

    authors: Liu Q,Sommer SS

    更新日期:2000-11-01 00:00:00

  • A hemagglutinating substance in chitin.

    abstract::Chitin from crustacean shells has often been used to isolate and purify plant lectins that have an affinity for poly-N-acetylglucosamine (poly-GlcNAc). When we used washed chitin from crab shells as an affinity medium to isolate a lectin from Pinus strobus L. (eastern white pine) ovules, we found that a substance havi...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Whitmore FA

    更新日期:1992-02-01 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

  • High-performance subtractive hybridization of cDNAs by covalent bonding between specific complementary nucleotides.

    abstract::We have developed an improved subtractive hybridization method that provides a fast, simple and reliable isolation of desired different sequences from two compared DNA libraries, one of which contains all unwanted homologues (subtracter) and another contains certain desired heterologues (tester). The DNA library can b...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/99265rr06

    authors: Ying SY,Lin S

    更新日期:1999-05-01 00:00:00

  • Alternative system for detection and mapping of activation domains.

    abstract::The ZEBRA protein is a transcriptional activator that induces expression of viral lytic genes in cells harboring latent Epstein-Barr virus (EBV). In this report it is shown that a derivative of ZEBRA that cannot activate transcription (Zd) can be used to detect and characterize activation domains. Three expression vec...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/97225rr02

    authors: Asković S,Baumann R

    更新日期:1997-05-01 00:00:00

  • Multicolor luciferase assay system: one-step monitoring of multiple gene expressions with a single substrate.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/05386ST03

    authors: Nakajima Y,Kimura T,Sugata K,Enomoto T,Asakawa A,Kubota H,Ikeda M,Ohmiya Y

    更新日期:2005-06-01 00:00:00

  • A mechanically strong matrix for protein electrophoresis with enhanced silver staining properties.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Patton WF,Lopez MF,Barry P,Skea WM

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  • 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

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  • Generation of a phagemid mouse recombinant antibody fragment library by multisite-directed mutagenesis.

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    journal_title:BioTechniques

    pub_type:

    doi:10.2144/03354st05

    authors: Kelley LL,Momany C

    更新日期:2003-10-01 00:00:00

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112169

    authors: Leitz AJ,Bayburt TH,Barnakov AN,Springer BA,Sligar SG

    更新日期:2006-05-01 00:00:00

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Lugert R,König H,Kurth R,Tönjes RR

    更新日期:1996-02-01 00:00:00

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114574

    authors: Persson H,Søkilde R,Pirona AC,Rovira C

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

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    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

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Fotadar U,Shapiro LE,Surks MI

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  • Universal SNP genotyping assay with fluorescence polarization detection.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/01313rr01

    authors: Hsu TM,Chen X,Duan S,Miller RD,Kwok PY

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Nehls M,Messerle M,Sirulnik A,Smith AJ,Boehm T

    更新日期:1994-10-01 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

  • Genetic immunization for antibody generation in research animals by intravenous delivery of plasmid DNA.

    abstract::Genetic immunization is an attractive approach to generate antibodies because native proteins are expressed in vivo with normal posttranscriptional modifications, avoiding time-consuming and costly antigen isolation or synthesis. Hydrodynamic tail or limb vein delivery of naked plasmid DNA expression vectors was used ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000112088

    authors: Bates MK,Zhang G,Sebestyén MG,Neal ZC,Wolff JA,Herweijer H

    更新日期:2006-02-01 00:00:00

  • Preparation of amino acid mixtures for cell-free expression systems.

    abstract::Here we present a procedure for preparing amino acid mixtures--having both the desired composition and a physiological pH--at high concentrations for cell-free expression systems. Up to 2.1 mg/mL of active protein was synthesized in batch mode reactions with an all Escherichia coli cell-free expression system. Our met...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114249

    authors: Caschera F,Noireaux V

    更新日期:2015-01-01 00:00:00

  • Express primer tool for high-throughput gene cloning and expression.

    abstract::High-throughput approaches for gene cloning and expression require the development of new nonstandard tools for molecular biologists and biochemists. We introduce a Web-based tool to design primers specifically for the generation of expression clones for both laboratory-scale and high-throughput projects. The applicat...

    journal_title:BioTechniques

    pub_type:

    doi:10.2144/02336bc03

    authors: Yoon JR,Laible PD,Gu M,Scott HN,Collart FR

    更新日期:2002-12-01 00:00:00

  • Green fluorescent protein as a reporter of gene expression and protein localization.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Kain SR,Adams M,Kondepudi A,Yang TT,Ward WW,Kitts P

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  • An improved strategy and a useful housekeeping gene for RNA analysis from formalin-fixed, paraffin-embedded tissues by PCR.

    abstract::Specific amplification of nucleic acid sequences by PCR has been extensively used for the detection of gene rearrangements and gene expression. Although successful amplification of DNA sequences has been carried out with DNA prepared from formalin-fixed, paraffin-embedded (FFPE) tissues, there are only a few reports r...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Finke J,Fritzen R,Ternes P,Lange W,Dölken G

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  • Cloning and expression of antigenic epitopes of the human 68-kDa (U1) ribonucleoprotein antigen in Escherichia coli.

    abstract::Autoantibodies directed against the 68-kDa (U1) ribonucleoprotein antigen are mainly found in sera of patients with mixed connective tissue disease. The corresponding cDNA was fragmented into four regions coding for the major antigenic epitopes A', B', C' and D'. All the epitopes were subcloned and expressed as fusion...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Frorath B,Scanarini M,Netter HJ,Abney CC,Liedvogel B,Lakomek HJ,Northemann W

    更新日期:1991-09-01 00:00:00

  • A simplified method for the production of recombinant baculovirus.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Goswami BB,Glazer RI

    更新日期:1991-05-01 00:00:00

  • A novel yeast-based recombination method to clone and propagate diverse HIV-1 isolates.

    abstract::Replication studies on human immunodeficiency virus 1 (HIV-1) rely on a few laboratory strains that are divergent from dominant HIV-1 subtypes in the epidemic. Several phenotypic differences between diverse HIV-1 isolates and subtypes could affect vaccine development and treatment, but this research field lacks robust...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000113119

    authors: Dudley DM,Gao Y,Nelson KN,Henry KR,Nankya I,Gibson RM,Arts EJ

    更新日期:2009-05-01 00:00:00

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    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Shapiro M

    更新日期:1995-06-01 00:00:00

  • Improved lysis of single bacterial cells by a modified alkaline-thermal shock procedure.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/000114389

    authors: He J,Du S,Tan X,Arefin A,Han CS

    更新日期:2016-03-01 00:00:00

  • Efficacy of an amphipathic oligopeptide to shuttle and release a cis-acting DNA decoy into human cells.

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/02321dd03

    authors: Citti L,Rovero P,Colombo MG,Mariani L,Poliseno L,Rainaldi G

    更新日期:2002-01-01 00:00:00

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/01302rr04

    authors: Tur MK,Huhn M,Sasse S,Engert A,Barth S

    更新日期:2001-02-01 00:00:00