Analysis of isoactin expression in cultured mouse cells by in situ hybridization
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Updated: Sep 15, 2026

A High Throughput in situ Hybridization Method to Characterize mRNA Expression Patterns in the Fetal Mouse Lower Urogenital Tract
Published on: August 19, 2011
1Division of Biochemistry, Chiba Cancer Center Research Institute, Japan.
Abstract:
The expression of cytoskeletal isoactin genes in NIH 3T3 and L cells was studied by in situ hybridization. Anti-sense RNA probes specific for beta- and gamma-actin were prepared by in vitro transcription of the 3'-untranslated regions of each cDNA which diverge in an isoactin-specific manner. Both NIH 3T3 and L cells showed a higher expression of beta- and gamma-actin mRNAs in a growing state than in a stationary one. Among these changes, the suppression of gamma-actin mRNA in L cells was most prominent and that of beta-actin in 3T3 cells was least profound.
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