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Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase.

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Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase. / Multhaupt, H; Fritz, P; Schumacher, K.

I: Histochemistry, Bind 87, Nr. 5, 1987, s. 465-70.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Multhaupt, H, Fritz, P & Schumacher, K 1987, 'Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase.', Histochemistry, bind 87, nr. 5, s. 465-70.

APA

Multhaupt, H., Fritz, P., & Schumacher, K. (1987). Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase. Histochemistry, 87(5), 465-70.

Vancouver

Multhaupt H, Fritz P, Schumacher K. Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase. Histochemistry. 1987;87(5):465-70.

Author

Multhaupt, H ; Fritz, P ; Schumacher, K. / Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase. I: Histochemistry. 1987 ; Bind 87, Nr. 5. s. 465-70.

Bibtex

@article{2fcaebd05d4411dd8d9f000ea68e967b,
title = "Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase.",
abstract = "Monoclonal antibodies against human liver arginase were raised in order to determine the exact distribution of arginase in human liver using a modified indirect unlabelled immunoperoxidase method. In normal human liver specific immunohistochemical staining was found in the cytoplasm of hepatocytes. Portal components (bile ducts and veins) and fibrous tissue were non-reactive, while erythrocytes were slightly positive. The specificity of the immunological reaction was confirmed by control tests. Spectrophotometry was used to quantitate the immunohistochemical reaction product, and the results indicated that arginase is homogeneously distributed in the liver lobule.",
author = "H Multhaupt and P Fritz and K Schumacher",
note = "Keywords: Animals; Antibodies, Monoclonal; Antibody Specificity; Arginase; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoenzyme Techniques; Liver; Mice; Mice, Inbred BALB C; Spectrophotometry",
year = "1987",
language = "English",
volume = "87",
pages = "465--70",
journal = "Histochemistry",
issn = "0301-5564",
publisher = "Springer",
number = "5",

}

RIS

TY - JOUR

T1 - Immunohistochemical localisation of arginase in human liver using monoclonal antibodies against human liver arginase.

AU - Multhaupt, H

AU - Fritz, P

AU - Schumacher, K

N1 - Keywords: Animals; Antibodies, Monoclonal; Antibody Specificity; Arginase; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoenzyme Techniques; Liver; Mice; Mice, Inbred BALB C; Spectrophotometry

PY - 1987

Y1 - 1987

N2 - Monoclonal antibodies against human liver arginase were raised in order to determine the exact distribution of arginase in human liver using a modified indirect unlabelled immunoperoxidase method. In normal human liver specific immunohistochemical staining was found in the cytoplasm of hepatocytes. Portal components (bile ducts and veins) and fibrous tissue were non-reactive, while erythrocytes were slightly positive. The specificity of the immunological reaction was confirmed by control tests. Spectrophotometry was used to quantitate the immunohistochemical reaction product, and the results indicated that arginase is homogeneously distributed in the liver lobule.

AB - Monoclonal antibodies against human liver arginase were raised in order to determine the exact distribution of arginase in human liver using a modified indirect unlabelled immunoperoxidase method. In normal human liver specific immunohistochemical staining was found in the cytoplasm of hepatocytes. Portal components (bile ducts and veins) and fibrous tissue were non-reactive, while erythrocytes were slightly positive. The specificity of the immunological reaction was confirmed by control tests. Spectrophotometry was used to quantitate the immunohistochemical reaction product, and the results indicated that arginase is homogeneously distributed in the liver lobule.

M3 - Journal article

C2 - 3323144

VL - 87

SP - 465

EP - 470

JO - Histochemistry

JF - Histochemistry

SN - 0301-5564

IS - 5

ER -

ID: 5240590