The Use of RT-PCR to Distinguish between Plasmid MnSOD Transcripts and Endogenous MnSOD mRNA

Jian-Jian Li, F. Domann, L. W. Oberley

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

We report here a convenient RT-PCR method to distinguish plasmid human MnSOD cDNA transcripts from the endogenous MnSOD gene products without engineering the cDNA insert. When a specific antisense primer for the carrier vector sequence was paired with a sense primer for the human MnSOD cDNA in RT-PCR analysis, a unique amplicon with the expected size was generated in MnSOD cDNA transfected cells but not in the wild type or vector control cells. The same primers were also used in genomic DNA-PCR to demonstrate genomic incorporation of cDNA in stably transfected cells. This method is convenient and specific in determining exogenous cDNA incorporation and expression in transfectants especially when transcripts of cDNA are difficult to separate from the endogenous mRNA by other methods.

Original languageEnglish (US)
Pages (from-to)610-618
Number of pages9
JournalBiochemical and Biophysical Research Communications
Volume216
Issue number2
DOIs
StatePublished - Nov 13 1995
Externally publishedYes

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Plasmids
Complementary DNA
Polymerase Chain Reaction
Messenger RNA
Genes
DNA

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology
  • Biophysics
  • Biochemistry

Cite this

The Use of RT-PCR to Distinguish between Plasmid MnSOD Transcripts and Endogenous MnSOD mRNA. / Li, Jian-Jian; Domann, F.; Oberley, L. W.

In: Biochemical and Biophysical Research Communications, Vol. 216, No. 2, 13.11.1995, p. 610-618.

Research output: Contribution to journalArticle

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