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Cathe

Manufactured by Biocare Medical

CATHE is a versatile laboratory instrument designed for automated cell analysis and counting. It utilizes advanced optical techniques to accurately measure and quantify various cell properties, including cell size, cell count, and cell viability. CATHE provides reliable and consistent results, supporting researchers and clinicians in their analytical workflows.

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2 protocols using cathe

1

Xenium Analyzer Tissue Staining Protocol

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After the run, slides were removed from the Xenium Analyzer instrument and had quencher removed according to 10X Genomics’ Demonstrated Protocol CG000613. Immediately following, the slides were H&E stained according to the following protocol: xylene (x3, 3min ea), 100% alcohol (x2, 2min ea), 95% alcohol (x2, 2min ea), 70% alcohol (2min), DI water rinse (1min), hematoxylin (1min) (Biocare Medical CATHE), DI water rinse (1min), bluing solution (1min) (Biocare Medical HTBLU-M), DI water rinse (3min), 95% alcohol (30sec), eosin (5sec) (Biocare Medical HTE-GL), 95% alcohol (10sec), 100% alcohol (x2, 10sec ea), xylene (x2, 10sec ea). Coverslipping was performed using Micromount (Leica 3801731) and cured overnight at room temperature. Histology images taken on a 20X Leica Biosystems Aperio CS2.
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2

Immunohistochemical Tumor Characterization

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Histological sections of tumor tissues were analyzed following H&E staining and additional immunostaining on selected sections to determine cell origins. IHC was performed on 4 μm slides of formalin-fixed and paraffin-embedded tumor tissue specimens. The sections were deparaffinized with changes of xylenes and graded ethanols to water. Antigen retrieval was performed in a Decloaking Chamber (Biocare) with Diva DeCloaker solution (Biocare Medical, DV 2004). Staining procedures were performed on a Biocare IntelliPath autostainer. Blocking was performed using Peroxidazed 1 (PX968, Biocare Medical) for 5 min, and Background Punisher (BP974, Biocare Medical) for 10 min. Sections were then incubated for 30 min at room temperature with a prediluted monoclonal antibody (Vimentin, SM Actin, MS Actin or Cytokeratin; Biocare Medical). Secondary antibody, mouse on canine polymer (Biocare Medical, MC541) was applied for 30 min. Finally, the chromagen, diaminobenzidine (DAB) was incubated for 5 min (IP FLX DAB, IPK5010, Biocare Medical) and followed by hematoxylin counterstain (CATHE, Biocare Medical) for 2 min. Negative controls were obtained by replacing the primary antibody with Polymer negative control serum (Biocare Medical, NC499) for 30 min.
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