2012
DOI: 10.1369/0022155412452146
|View full text |Cite
|
Sign up to set email alerts
|

Application of Immunohistochemical Staining to Detect Antigen Destruction as a Measure of Tissue Damage

Abstract: During the late 19th century, a number of dye types were used in early microscopic investigations of simple plant and tissue materials (Cook 1997). These included (1) hematoxylin and eosin (H&E) used separately, (2) picric acid and carmine used concurrently, and, finally, (3) the combination of H&E (Cook 1997;Gill 2010). The H&E staining method evolved rapidly into a traditional staining standard used for morphological study within histology and cytology settings throughout the world (Cook 1997;Shi et al. 2011… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
13
0

Year Published

2013
2013
2024
2024

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 18 publications
(13 citation statements)
references
References 13 publications
0
13
0
Order By: Relevance
“…Sections were incubated in appropriate blocking serum and then treated with primary antibodies [biotinylated anti-swine IgG (Vector Laboratories, Inc., Burlingame, CA; Catalogue BA-9020, dilution 1 : 100) or anti-A␤ 42 (Millipore Corporation, Billerica, MA; Catalogue # AB5078P; dilution 1 : 50)] for 1 h at room temperature. The specificity of the antibodies used has already been verified [48][49][50]. After a thorough rinse in PBS, sections probed with anti-A␤ 42 were then probed with biotin-labeled secondary antibody (anti-rabbit IgG, Vector Laboratories, Inc.;…”
Section: Immunohistochemistrymentioning
confidence: 99%
“…Sections were incubated in appropriate blocking serum and then treated with primary antibodies [biotinylated anti-swine IgG (Vector Laboratories, Inc., Burlingame, CA; Catalogue BA-9020, dilution 1 : 100) or anti-A␤ 42 (Millipore Corporation, Billerica, MA; Catalogue # AB5078P; dilution 1 : 50)] for 1 h at room temperature. The specificity of the antibodies used has already been verified [48][49][50]. After a thorough rinse in PBS, sections probed with anti-A␤ 42 were then probed with biotin-labeled secondary antibody (anti-rabbit IgG, Vector Laboratories, Inc.;…”
Section: Immunohistochemistrymentioning
confidence: 99%
“…Tissue damage resulting in cell death can occur without observable morphological changes, and this may not be revealed through routine histological methods. 23 That is why in the current study, IHC was used to evaluate both cellular and acellular components of hyaline cartilage separately. IHC provides more in-depth information on a particular sample, plus more detailed information on the presence and localization of certain substances (normal or abnormal) in cells or tissues, as well as number of molecules.…”
Section: Discussionmentioning
confidence: 99%
“…The immunoreaction was evaluated according to the estimated staining intensity according to the following parameter: 0 = no staining, + = weak staining, ++ = moderate staining, +++ = strong staining, and ++++ = very strong staining. 0 and + are considered negative (low level) while ++, +++ and ++++ are considered positive (high level) [13] .…”
Section: Immunohistochemistrymentioning
confidence: 99%