Delivery of protein into cells using polycationic liposomes.

Abstract:

:We describe a procedure for delivery of purified proteins into a variety of tissue culture cells using a new polycationic lipid preparation, LipofectAMINE. Several different proteins, with diverse physical properties, can be delivered into cells by this method. Compared with commercially available monocationic lipids, protein delivery using LipofectAMINE is more efficient. Unlike other methods for protein delivery, the lipofection procedure is simple, inexpensive and effective for both adherent and nonadherent cell types. Proteins introduced into cells using this method are shown to be biochemically and biologically active.

journal_name

Biotechniques

journal_title

BioTechniques

authors

Sells MA,Li J,Chernoff J

subject

Has Abstract

pub_date

1995-07-01 00:00:00

pages

72-6, 78

issue

1

eissn

0736-6205

issn

1940-9818

journal_volume

19

pub_type

  • Surveying the repair of ancient DNA from bones via high-throughput sequencing.

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    authors: Mouttham N,Klunk J,Kuch M,Fourney R,Poinar H

    更新日期:2015-07-01 00:00:00

  • A program for computer-assisted scoring of Southern blots.

    abstract::SCORE, a program for computer-assisted scoring of Southern blots of clone DNA, retains the use of expert human judgment while taking over much of the drudgery of the scoring task. The primary functions of the program are to help make an aligned overlay of the fluorescence gel image and the autoradiogram blot image, to...

    journal_title:BioTechniques

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    doi:

    authors: Cannon TM,Koskela RJ,Burks C,Stallings RL,Ford AA,Hempfner PE,Brown HT,Fickett JW

    更新日期:1991-06-01 00:00:00

  • Method for linking a synthesized protein to its mRNA-DNA complex.

    abstract::A nascent protein remains in a complex with its ribosome and mRNA if the stop codon is deleted from the mRNA. In the same manner, mRNA forms a stable complex with DNA if the transcription termination is blocked. In principle, if both mRNA translation and DNA transcription termination are prevented, the protein should ...

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:10.2144/00294st06

    authors: Liu S,Shivashankar GV,Sano T,Libchaber A

    更新日期:2000-10-01 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

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

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    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

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Copley CG,Boot C

    更新日期:1992-12-01 00:00:00

  • Graphene veils: A versatile surface chemistry for sensors.

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    journal_title:BioTechniques

    pub_type: 杂志文章

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    更新日期:2014-07-01 00:00:00

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    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Joshi AK,Baichwal V,Ames GF

    更新日期:1991-01-01 00:00:00

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    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

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    doi:10.2144/98246cr04

    authors: Sasaki CY,Passaniti A

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    pub_type: 杂志文章

    doi:

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

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  • CRISPR vs COVID-19: how can gene editing help beat a virus?

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    authors: Damude S,Muller Kobold AC,Bastiaannet E,Kruijff S,Hoekstra HJ,Wevers KP

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    abstract::We describe here a simple and efficient transfection method for transient expression of cloned genes in cell lines and primary cultured cells. The method involves the use of DEAE-dextran to target DNA to the cellular endocytotic pathway and the use of a human adenovirus to ensure efficient lysis of endosomal vesicles....

    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Forsayeth JR,Garcia PD

    更新日期:1994-08-01 00:00:00

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    journal_title:BioTechniques

    pub_type: 杂志文章

    doi:

    authors: Mitchell BW,Palmieri S

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  • Eukaryotic GST fusion vector for the study of protein-protein associations in vivo: application to interaction of ATFa with Jun and Fos.

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    journal_title:BioTechniques

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    doi:

    authors: Lindquist S,Hansson L,Hernell O,Lönnerdal B,Normark J,Strömquist M,Bergström S

    更新日期:1994-10-01 00:00:00

  • Generation of Flp-intm-ready DG44 and Lec 3.2.8.1 CHO cell lines for quick and easy constitutive protein expression.

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    journal_title:BioTechniques

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    authors: Texier P,Coddeville M,Bordes P,Genevaux P

    更新日期:2018-09-01 00:00:00

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    authors: Vang S,Seitz K,Krysan PJ

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    authors: Schmidt M,Grey M,Brendel M

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  • Direct RT-PCR amplification of mRNA supported on membranes.

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    journal_title:BioTechniques

    pub_type:

    doi:

    authors: Ruiz A,Bok D

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    pub_type: 杂志文章

    doi:10.2144/99264st08

    authors: Reddy LV,DeSilva R,Handley RS,Schaap AP,Akhavan-Tafti H

    更新日期:1999-04-01 00:00:00