Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue. / Kirkeby, S.

In: Acta Histochemica, Vol. 68, No. 1, 1981, p. 111-6.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Kirkeby, S 1981, 'Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue', Acta Histochemica, vol. 68, no. 1, pp. 111-6.

APA

Kirkeby, S. (1981). Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue. Acta Histochemica, 68(1), 111-6.

Vancouver

Kirkeby S. Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue. Acta Histochemica. 1981;68(1):111-6.

Author

Kirkeby, S. / Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue. In: Acta Histochemica. 1981 ; Vol. 68, No. 1. pp. 111-6.

Bibtex

@article{77474770f68b11ddbf70000ea68e967b,
title = "Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue",
abstract = "In tissue decalcified with MgNa2EDTA at a neutral pH activity for ATPase can used be for demonstration of the vascular structures at the muscle-bone interface. The GOMORI method for alkaline phosphatase is only of value, when fresh unfixed tissue is to be examined. The azo-dye method for alkaline phosphatase failed to give satisfactory results, and so did the alpha-amylase PAS method. 5'-nucleotidase activity is present in both capillaries and in cells lining the surfaces of bones, while larger blood vessels are poorly stained.",
author = "S Kirkeby",
note = "Keywords: 5'-Nucleotidase; Adenosine Triphosphatases; Alkaline Phosphatase; Amylases; Animals; Bone and Bones; Capillaries; Histocytochemistry; Muscles; Nucleotidases; Rats; Staining and Labeling; alpha-Amylases",
year = "1981",
language = "English",
volume = "68",
pages = "111--6",
journal = "Acta Histochemica",
issn = "0065-1281",
publisher = "Elsevier GmbH - Urban und Fischer",
number = "1",

}

RIS

TY - JOUR

T1 - Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue

AU - Kirkeby, S

N1 - Keywords: 5'-Nucleotidase; Adenosine Triphosphatases; Alkaline Phosphatase; Amylases; Animals; Bone and Bones; Capillaries; Histocytochemistry; Muscles; Nucleotidases; Rats; Staining and Labeling; alpha-Amylases

PY - 1981

Y1 - 1981

N2 - In tissue decalcified with MgNa2EDTA at a neutral pH activity for ATPase can used be for demonstration of the vascular structures at the muscle-bone interface. The GOMORI method for alkaline phosphatase is only of value, when fresh unfixed tissue is to be examined. The azo-dye method for alkaline phosphatase failed to give satisfactory results, and so did the alpha-amylase PAS method. 5'-nucleotidase activity is present in both capillaries and in cells lining the surfaces of bones, while larger blood vessels are poorly stained.

AB - In tissue decalcified with MgNa2EDTA at a neutral pH activity for ATPase can used be for demonstration of the vascular structures at the muscle-bone interface. The GOMORI method for alkaline phosphatase is only of value, when fresh unfixed tissue is to be examined. The azo-dye method for alkaline phosphatase failed to give satisfactory results, and so did the alpha-amylase PAS method. 5'-nucleotidase activity is present in both capillaries and in cells lining the surfaces of bones, while larger blood vessels are poorly stained.

M3 - Journal article

C2 - 6167124

VL - 68

SP - 111

EP - 116

JO - Acta Histochemica

JF - Acta Histochemica

SN - 0065-1281

IS - 1

ER -

ID: 10208912