ORIGINAL ARTICLES APPLICATION OF SILVER ACETATE AUTOMETALLOGRAPHY AND GOLD-SILVER STAINING METHODS FOR IN SITU DNA HYBRIDIZATION

被引:0
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作者
GW Hacker
AH Graf
C Hauser-Kronberger
G Wirnsberger
A Schiechl
G Bernatzky
U Wittauer
苏慧慈
H Adam
J Thurner
G Danscher
L Grimelius
机构
[1] Landeskrankenanstalten Salzburg,Institute of Pathological Anatomy,Immunohistochemistry and Biochemistry Unit,Salzburg,Austria
[2] University of Graz,Institute of PatholOgical Anatomy,Graz.Austria
[3] University of Salzburg,Institute of Zoology,Salzburg,Auatria
[4] University of Salzburg,Institute of Zoology,Salzburg,Austria
[5] Department of Histology and Embryology,Fourth Military Medical University,Xi’an,Shaanxi,PR China
[6] Landeskrankenanstalten Salzburg,Institute Of Pathological Anatomyy,Immunohistochemistry and Biochemistry Unit,Salzburg,Austria
[7] University of Aarhus,Institute of Anatomy,Department of Neurobiology,Aarhus,Denmark
[8] Uppsala University Hospital,Institute of Pathology,Uppsala,Sweden
基金
瑞典研究理事会;
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D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
In situ hybridization using biotinylated DNA probes hasbecome an important tool in histopathology.It is well knownthat the sensitivity of the methods used to demonstrate viralDNA in formalin-fixed and paraffin-embedded specimen de-pends strongly on the detection system used.In the presentstudy,an optimized in situ DNA hybridization protocol wascombined with four different approaches of gold-silver stainingmethods.For silver enhancement,the recently described meth-od of silver acetate autometallography,a technique allowinghighly efficient development without the necessity of dark roomillumination has been used.The most efficient detection methodfound in our experiments was the use of gold-adsorbedanti-biotin antibodies with subsequent silver enhancement.Thisstaining procedure can be completed in 5 hours includinghybridization and is a highly sensitive alternative to peroxidaseand alkaline phosphatase detection systems.
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页码:83 / 92
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