Comparative studies in efficiency of expression of bacterial β-galactosidase in vivo by the immunofluorescence method

Authors

  • S. P. Shpilevaya Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • I. E. Kostetsky Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • L. I. Likhacheva Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • L. G. Zharova Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • D. M. Irodov Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • E. V. Usenko Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • T. V. Stolyar Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author
  • V. A. Kordium Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR Kiev, USSR Author

DOI:

https://doi.org/10.7124/bc.000249

Abstract

The expression of some vector molecules encoding the synthesis of bacterial p-galactosidase in mouse liver hepatocytes 24 h after direct injection has been investigated. The advantages of immunofluorescence method with the microcytophotometry for rapid test of gene expression at the cell level are discussed.

References

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Published

1990-01-20

Issue

Section

Biopolymers and Cell