A method for establishing cell lines from Drosophila melanogaster embryos

In Vitro. 1977 Jan;13(1):36-40. doi: 10.1007/BF02615502.

Abstract

A simple method is presented for establishing continuous cell lines from Drosophila melanogaster embryos. Subculturing is performed after the first 8 weeks and at 2-week intervals thereafter. Initial plating densities of 5 x 10(4) to 5 x 10(5) cells per cm2 are required for maintaining the subcultures. Cell lines were established from wild-type embryos, from embryos bearing chromosomal rearrangements and from embryos bearing recessive mutations. Permanent lines have doubling times of 24 to 48 hr and have been maintained for as long as 13 months and 25 subcultures.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Division
  • Cell Line*
  • Chromosomes
  • Culture Media
  • Cytological Techniques
  • Drosophila melanogaster / embryology*
  • Genes, Recessive
  • Insulin
  • Sex Chromosomes
  • Translocation, Genetic

Substances

  • Culture Media
  • Insulin