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Ema clone e29

Manufactured by Roche

The EMA (clone E29) is a laboratory equipment product offered by Roche. It is a monoclonal antibody that can be used for the detection and analysis of certain cellular markers. The core function of the EMA (clone E29) is to provide a tool for researchers and clinicians to study and characterize specific cell types or cellular processes. However, a more detailed and unbiased description of the product's features and intended use cannot be provided while maintaining the requested approach.

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3 protocols using ema clone e29

1

Immunohistochemical Staining Protocols for Pathological Analysis

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The immunohistochemical stains were performed at the Department of Pathology, MSKCC, using commercially available antibodies. Staining for pan-cytokeratin (clone AE1/AE3, Dako, 1:1600), EMA (clone E29, Ventana, pre-diluted), S100 (polyclonal, Dako, 1:8000), INI-1/BAF-47 (clone 25/BAF47, BD Bioscience, 1:200) were performed on the automated Ventana BenchMark ULTRA immunostainer (Roche, Indianapolis, IN), using OptiView DAB IHC Detection Kit (Ventana Medical Systems, Tucson, AZ). Staining for Brachyury (clone EPR18113, Abcam, 1:500) was performed on the Leica Bond-3 immunostainer (Leica, Buffalo Grove, IL), using a polymer detection system (DS9800; Leica, Bond Polymer Refine Detection).
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2

Immunohistochemical Profiling of Tissue Samples

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Immunohistochemistry was conducted in 5 μm formalin-fixed
paraffin-embedded (FFPE) whole tissue sections. Staining for CK7 (clone OV-TL
12/30, DAKO, 1:800), AMACR (clone 12H4, Zeta Corp, 1:100), CD10 (clone SP67,
Ventana), EMA (clone E29, Ventana), CD15 (clone MMA, Ventana) and Pax8
(Proteintech, 1:100) was performed using a BenchMark XT automated system
(Ventana, Tucson, AZ). Staining for YAP/TAZ (D24E4, Cell Signaling Technology,
1:50) was performed using an automated Ventana Discovery system (Ventana).
Immunostaining scores (H-scores) for YAP/TAZ nuclear staining were determined as
[H= intensity (0–3) x percentage of positive cells (1–100)].
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3

Immunohistochemical Profiling of Tissue Samples

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The tissue slides were deparaffinized in xylene, hydrated in alcohol, and baked in a microwave (30 min in Tris buffer pH 9). Endogenous peroxidase was blocked. Staining was performed on the Benchmark ultra-automated stainer (Ventana) using diamino-benzidine as chromogen (Dako, Glostrup, Denmark). The following antibodies were used: AE1/E3 (clone PCK26, Ventana), KL1 (clone KL1, HIS-TOLS reagent), EMA (clone E29, Ventana), P63 (4A4, Ventana), S100 protein (clone poly Z311, Dako), SOX10 (EP268, BioSB), Desmin (clone DE-R11, Ventana), Myogenin (clone LO26, Leica), MYOD1 (clone EP212, Cell marque), ALK (clones D5F3, Cell Signaling Technology and clone 1A4, Novocastra), CD99/MIC2 (12E7, Dako), ETV4 (clone 16, Santa Cruz), CD30 (BerH2, Dako), CD4 (4B12, Novocastra), and CD7 (SP94, Ventana).
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