2019
DOI: 10.3233/cbm-181911
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TROY expression is associated with pathological stage and poor prognosis in patients treated with radical cystectomy

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Cited by 3 publications
(3 citation statements)
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“…We sliced 10% formalin‐fixed and paraffin‐embedded tissues and cell lines into 3 μm thick sections and stained them with hematoxylin and eosin. To evaluate GAL3 expression, these sections were additionally immunostained using the Bond‐MAX Automated Immunohistochemistry system and Bond Polymer Refine Detection Kit (DC 9800; Leica Biosystems) based on our previous study with minor modifications 19 . First, the sections were deparaffinized and pretreated with Bond Epitope Retrieval Solution 2 (Leica Biosystems) at 100°C for 20 min.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…We sliced 10% formalin‐fixed and paraffin‐embedded tissues and cell lines into 3 μm thick sections and stained them with hematoxylin and eosin. To evaluate GAL3 expression, these sections were additionally immunostained using the Bond‐MAX Automated Immunohistochemistry system and Bond Polymer Refine Detection Kit (DC 9800; Leica Biosystems) based on our previous study with minor modifications 19 . First, the sections were deparaffinized and pretreated with Bond Epitope Retrieval Solution 2 (Leica Biosystems) at 100°C for 20 min.…”
Section: Methodsmentioning
confidence: 99%
“…To evaluate GAL3 expression, these sections were additionally immunostained using the Bond-MAX Automated Immunohistochemistry system and Bond Polymer Refine Detection Kit (DC 9800; Leica Biosystems) based on our previous study with minor modifications. 19 First, the sections were deparaffinized and pretreated with Bond Epitope Retrieval Solution 2 (Leica Biosystems) at 100 C for 20 min. After washing, peroxidase blocking was performed for 10 min.…”
Section: Evaluation Of Immunohistochemical Stainmentioning
confidence: 99%
“…Formalin-fixed (10%) and paraffin-embedded tissues were processed into 3-μm-thick sections. Immunohistochemical staining was performed using a Leica Bond-Max automated system and the BOND polymer Refine Detection Kit (Leica Biosystems, Bannockburn, IL), based on the previous report of Nomura et al (26). Tissues were first deparaffinized with AutoDewaxer and antigens were retrieved with BOND Epitope Retrieval Solution 2 at 100°C for 20 min.…”
Section: Methodsmentioning
confidence: 99%