Literature DB >> 2438258

Metachromasia of 3-amino-9-ethylcarbazole (AEC) and its prevention in immunoperoxidase techniques.

K Koretz, J Leman, I Brandt, P Möller.   

Abstract

3-Amino-9-ethylcarbazole (AEC) used as chromogen in immunoperoxidase techniques normally has an intense, red colour. However, as an inconstant phenomenon, a pale yellowish-green reaction product severely impairing the evaluation can be observed. In order to circumvent this undesired effect, factors such as tissue fixative, proteolytic digestion, antibody concentrations and incubation time of the primary antibody were analyzed. The most important factor inducing a change in colour is probably the inadequately high local peroxidase concentration arising as the consequence of high amounts of bound primary antibody. This high enzyme concentration might cause metachromasia of AEC by producing the yellowish-green quinone-di-imine form of the substrate. As could be shown by spectrophotometry in test tube experiments, AEC metachromasia was proven to be enzyme dependent. Thus, the best way to trigger the local enzyme concentration on a tissue section to adequate levels appears to be the dilution of the primary antibody.

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Year:  1987        PMID: 2438258     DOI: 10.1007/bf00500619

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  31 in total

1.  Purification of horse-radish peroxidase and comparison of its properties with those of catalase and methaemoglobin.

Authors:  D KEILIN; E F HARTREE
Journal:  Biochem J       Date:  1951-06       Impact factor: 3.857

2.  The effects of preliminary proteolysis on the immunohistochemical and dye staining properties of elastic fibres.

Authors:  S L Mera; F Lovett; J D Davies
Journal:  Histochem J       Date:  1985-02

3.  The use of proteolytic enzymes to improve immunoglobulin staining by the PAP technique.

Authors:  B L Mepham; W Frater; B S Mitchell
Journal:  Histochem J       Date:  1979-05

4.  Immunohistochemical demonstration of hepatitis B core and surface antigens in paraffin sections.

Authors:  S N Huang
Journal:  Lab Invest       Date:  1975-07       Impact factor: 5.662

5.  A digestion technique for the reduction of background staining in the immunoperoxidase method.

Authors:  M Reading
Journal:  J Clin Pathol       Date:  1977-01       Impact factor: 3.411

6.  Immunoperoxidase staining of formalin-fixed, paraffin-embedded, human renal biopsies with a comparison of the peroxidase-antiperoxidase (PAP) and indirect methods.

Authors:  R A Sinclair; J Burns; M S Dunnill
Journal:  J Clin Pathol       Date:  1981-08       Impact factor: 3.411

7.  The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique.

Authors:  R C Graham; M J Karnovsky
Journal:  J Histochem Cytochem       Date:  1966-04       Impact factor: 2.479

8.  Sensitivity of various visualization methods for peroxidase and alkaline phosphatase activity in immunoenzyme histochemistry.

Authors:  A S De Jong; M Van Kessel-van Vark; A K Raap
Journal:  Histochem J       Date:  1985-10

9.  The horseradish peroxidase-catalyzed oxidation of 3,5,3',5'-tetramethylbenzidine. Free radical and charge-transfer complex intermediates.

Authors:  P D Josephy; T Eling; R P Mason
Journal:  J Biol Chem       Date:  1982-04-10       Impact factor: 5.157

10.  A comparison of eight different chromogen protocols for the demonstration of immunoreactive neurofilaments or glial filaments in rat cerebellum using the peroxidase-antiperoxidase method and monoclonal antibodies.

Authors:  J Q Trojanowski; M A Obrocka; V M Lee
Journal:  J Histochem Cytochem       Date:  1983-10       Impact factor: 2.479

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  1 in total

Review 1.  Towards a systems understanding of MHC class I and MHC class II antigen presentation.

Authors:  Jacques Neefjes; Marlieke L M Jongsma; Petra Paul; Oddmund Bakke
Journal:  Nat Rev Immunol       Date:  2011-11-11       Impact factor: 53.106

  1 in total

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