Skip to main content

Antibodies to Allozymes as Potential Cell Markers for Chimeric Mouse Studies

  • Chapter
Genetic Mosaics and Chimeras in Mammals

Part of the book series: Basic Life Sciences ((BLSC,volume 12))

Abstract

The limiting factor in the use of mouse chimeras for the revelation of detailed fate maps during embryogenesis is the lack of suitable cell marker systems. This limitation is evident when the list of available chimeric or mosaic markers is examined and compared to the criteria for an ideal marker system. An ideal cell marker should (1) be expressed in all descendants of a cell; (2) be present in all cells of a tissue or organism; (3) be cell autonomous; (4) be cell localized; (5) exist in variant forms which are selectively neutral; (6) have variant forms which can be detected in histologic sections; and (7) have variants which are expressed early in embryogenesis.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

eBook
USD 16.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Askenase, P. W. and E. J. Leonard. 1970. Solid phase radioimmunoassay of human β-1C globulin. Immunochem. 7: 29–41.

    Article  CAS  Google Scholar 

  • Chapman, V. M., W. K. Whitten and F. H. Ruddle. 1971. Expression of paternal glucosephosphate isomerase-1 (GPI-1) in preimplantation mouse embryos. Devel. Biol. 26: 153–158.

    Article  CAS  Google Scholar 

  • Condamine, H., R. P. Custer and B. Mintz. 1971. Pure-strain and genetically mosaic liver tumors histochemically identified with the β-glucuronidase marker in allophenic mice. Proc. Nat. Acad. Sci., USA 68: 2032–2036.

    Article  CAS  Google Scholar 

  • Cuatrecasas, P. 1970. Protein purification by affinity chromatography. Derivations of agarose and Polyacrylamide beads. J. Biol. Chem. 245: 3059–3065.

    PubMed  CAS  Google Scholar 

  • DeLorenzo, R. J. and F. H. Ruddle. 1969. Genetic control of two electrophoretic variants of glucosephosphate isomerase in the mouse (Mus musculus). Biochem. Genet. 3: 151–162.

    Article  PubMed  CAS  Google Scholar 

  • Dewey, M. J., A. G. Gervais and B. Mintz. 1976. Brain and ganglion development from two genotypic classes of cells in allophenic mice. Devel. Biol. 50: 68–81.

    Article  CAS  Google Scholar 

  • Feder, N. 1976. Solitary cells and enzyme exchange in tetraparental mice. Nature 263: 67–69.

    Article  PubMed  CAS  Google Scholar 

  • Gearhart, J. D. and B. Mintz. 1972. Clonal origins of somites and their muscle derivatives: Evidence from allophenic mice. Devel. Biol. 29: 27–37.

    Article  CAS  Google Scholar 

  • Gearhart, J. and M. L. Oster-Granite. 1978. Isolation of glucosephosphate isomerase from mouse tissues and the obtainment of anti-GPI antisera. Submitted for publication.

    Google Scholar 

  • Herrup, K. and R. J. Mullen. 1977. Biochemical and genetic factors in the heat inactivation of murine-β-glucuronidase. Biochem. Genet. 15: 641–653.

    Article  PubMed  CAS  Google Scholar 

  • Hunter, W. M. and F. C. Greenwood, 1962. Preparation of iodine-131 labeled human growth hormone of high specific activity. Nature 194: 495–496.

    Article  PubMed  CAS  Google Scholar 

  • McLaren, A. 1976. Mammalian Chimaeras. Cambridge University Press, Cambridge, Great Britain.

    Google Scholar 

  • Mintz, B. 1974. Gene control of mammalian differentiation. Ann. Rev. Genet. 8: 411–470.

    Article  PubMed  CAS  Google Scholar 

  • Mullen, R. J. 1977. Genetic dissection of the CNS with mutant-normal mouse and rat chimeras, In Soc. Neurosci. Symp. 2: 47–65. W. M. Cowan and J. A. Ferendelli, eds.

    Google Scholar 

  • Mullen, R. J. 1978. Presented at this conference.

    Google Scholar 

  • Padua, R. A., G. Bulfield and J. Peters. 1978. Biochemical genetics of a new glucosephosphate isomerase allele (Gpi-1 c ) from wild mice. Biochem. Genet. 16: 127–143.

    Article  PubMed  CAS  Google Scholar 

  • Phillips, T. L., J. M. Talent and R. W. Gracy. 1976. Isolation of rabbit glucosephosphate isomerase by a single-step substrate elution. Biochem. Biophys. Acta 429: 624–628.

    PubMed  CAS  Google Scholar 

  • Rodriguez, J. and F. Deinhardt. 1960. Preparation of a semipermanent mounting medium for fluorescent antibody studies. Virology 12: 316–317.

    Article  PubMed  CAS  Google Scholar 

  • Sainte-Marie, G. 1962. A paraffin embedding technique for studies employing immunofluorescence. J. Histochem. Cytochem. 10: 250–256.

    Article  Google Scholar 

  • Swank, R. T., K. Paigen and R. E. Ganschow. 1974. Genetic control of glucuronidase induction in mice. J. Mol. Biol. 81: 225–243.

    Article  Google Scholar 

  • Yellin, H. and L. Guth. 1970. The histochemical classification of muscle fibers. Exper. Neurol. 26: 424–432.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1978 Plenum Press, New York

About this chapter

Cite this chapter

Gearhart, J., Oster-Granite, M.L. (1978). Antibodies to Allozymes as Potential Cell Markers for Chimeric Mouse Studies. In: Russell, L.B. (eds) Genetic Mosaics and Chimeras in Mammals. Basic Life Sciences, vol 12. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-3390-6_9

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-3390-6_9

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-3392-0

  • Online ISBN: 978-1-4684-3390-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics