Literature DB >> 1313387

Measurement of hygromycin B phosphotransferase activity in crude mammalian cell extracts by a simple dot-blot assay.

M S Sørensen1, M Duch, K Paludan, P Jørgensen, F S Pedersen.   

Abstract

Hygromycin B (Hy) resistance, encoded by the prokaryotic gene hph, is commonly used as a dominant selectable marker for gene transfer experiments in mammalian cells. We describe a simple, quantitative dot-blot assay for measuring the activity in crude mammalian cell extracts of Hy phosphotransferase, the product of the hph gene. The assay shows no cross interference with substrates for neomycin phosphotransferase II, the product of the commonly used marker gene neo; hph and neo may thus be useful as a set of two non-interfering selectable marker and reporter genes for gene transfer experiments in mammalian cells.

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Year:  1992        PMID: 1313387     DOI: 10.1016/0378-1119(92)90386-4

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  5 in total

1.  Mutated primer binding sites interacting with different tRNAs allow efficient murine leukemia virus replication.

Authors:  A H Lund; M Duch; J Lovmand; P Jørgensen; F S Pedersen
Journal:  J Virol       Date:  1993-12       Impact factor: 5.103

2.  A UV-induced mutation in neurospora that affects translational regulation in response to arginine.

Authors:  M Freitag; N Dighde; M S Sachs
Journal:  Genetics       Date:  1996-01       Impact factor: 4.562

3.  A correlation between dexamethasone inducibility and basal expression levels of retroviral vector proviruses.

Authors:  M Duch; K Paludan; J Lovmand; L Pedersen; P Jørgensen; F S Pedersen
Journal:  Nucleic Acids Res       Date:  1993-10-11       Impact factor: 16.971

4.  Expression of hygromycin phosphotransferase alters virulence of Histoplasma capsulatum.

Authors:  A George Smulian; Reta S Gibbons; Jeffery A Demland; Deborah T Spaulding; George S Deepe
Journal:  Eukaryot Cell       Date:  2007-09-14

5.  Purification and characterization of aminoglycoside phosphotransferase APH(6)-Id, a streptomycin-inactivating enzyme.

Authors:  Meseret Ashenafi; Tatiana Ammosova; Sergei Nekhai; W Malcolm Byrnes
Journal:  Mol Cell Biochem       Date:  2013-11-19       Impact factor: 3.396

  5 in total

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