[15] Immunohistochemical detection of metallothionein

https://doi.org/10.1016/0076-6879(91)05091-9Get rights and content

First page preview

First page preview
Click to open first page preview

References (31)

  • F.O. Brady et al.

    Anal. Biochem.

    (1979)
  • R.K. Mehra et al.

    Biochem. J.

    (1983)
  • D. Banerjee et al.

    Toxicology

    (1982)
  • C. Tohyama et al.

    Acta Histochem. Cytochem.

    (1988)
  • M.E. Elmes et al.

    J. Pathol.

    (1989)
  • W. Savino et al.

    J. Histochem. Cytochem.

    (1984)
  • J. Gwyn-Jones et al.

    Scand. J. Gastroenterol. Suppl.

    (1981)
  • C.F.A. Culling et al.

    Cellular Pathology Techniques

    C.F.A. Culling et al.

    Cellular Pathology Techniques

  • A.F.W. Morselt et al.

    Arch. Toxicol.

    (1984)
  • R.S. Vander Mallie et al.

    Immunocytochemistry

    (1978)
  • S. Ohi et al.

    J. Biol. Chem.

    (1981)
  • D.R. Winge et al.
  • Y. Kikuchi et al.

    Mol. Immunol.

    (1988)
  • K.G. Danielson et al.
  • J.P. Clarkson et al.

    Histochem. J.

    (1985)
  • Cited by (86)

    • Spatial expression of metallothionein, matrix metalloproteinase-1 and Ki-67 in human epidermal wounds treated with zinc and determined by quantitative immunohistochemistry: A randomised double-blind trial

      2021, European Journal of Cell Biology
      Citation Excerpt :

      In contrast to MMP-1, MT was induced in the wound bed and in NHDFs in response to ZnSO4. The anti-MT antibody used for immunohistochemical quantification reacts with a conserved and shared N-epitope of MT1 and MT2 (Jasani and Elmes, 1991). There are 8 functional human MT1 subisoforms (MT1A, MT1B, MT1E, MT1F, MT1G, MT1H, MT1M, and MT1X) and 1 MT2 subisoform (MT2A).

    • Prognostic significance of metallothionein in B-cell lymphomas

      2006, Blood
      Citation Excerpt :

      Group comparisons were done using 2-sided, paired Student t test (equal variance assumed). Sections of formalin-fixed, paraffin-embedded biopsies were heated in a Milestone Micromed microwave oven (Sorisole, Italy) in citrate buffer (pH 6) for 15 minutes, incubated 60 minutes at room temperature with a 1:40 dilution of DAKO-MT (clone, E9; DAKO, Carpinteria, CA) reactive with MT-I and MT-II in routinely processed histologic samples,13 and stained in the Techmate 500 Immunostainer (DAKO, Glostrup, Denmark), using the DAKO Envision K5007 as a secondary antibody. Since the results suggested that some of the MT-positive cells represented macrophages, samples were also stained using CD68 (PGM1) on adjacent sections.

    • Evaluation of MT expression and detection of apoptotic cells in LEC rat kidneys

      2004, Biochimica et Biophysica Acta - Molecular Basis of Disease
    • Metallothionein in bovine spongiform encephalopathy

      2002, Journal of Comparative Pathology
    View all citing articles on Scopus
    View full text