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Lucerna-Chem ag ly300328
Ly300328, supplied by Lucerna-Chem ag, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ly300328/ly300328/pm32330455-408-34-35
Average 90 stars, based on 1 article reviews
ly300328 - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Expressing:

Article Title: Cathepsin S Regulates Antigen Processing and T Cell Activity in Non-Hodgkin Lymphoma.
Article Snippet: At the end of the B cell/T cell co-culture, cells were collected, stained with PE-Cy7 anti-mouse CD8a antibody (Clone 53-6.7, BD Biosciences, San Jose, CA, USA cat #552877) and analyzed for the proliferation of T cells stained by quantifying CellTrace violet proliferation peaks using flow cytometry.

Staining:

Article Title: Cathepsin S Regulates Antigen Processing and T Cell Activity in Non-Hodgkin Lymphoma.
Article Snippet: At the end of the B cell/T cell co-culture, cells were collected, stained with PE-Cy7 anti-mouse CD8a antibody (Clone 53-6.7, BD Biosciences, San Jose, CA, USA cat #552877) and analyzed for the proliferation of T cells stained by quantifying CellTrace violet proliferation peaks using flow cytometry.

Isolation:

Article Title: Cathepsin S Regulates Antigen Processing and T Cell Activity in Non-Hodgkin Lymphoma.
Article Snippet: At the end of the B cell/T cell co-culture, cells were collected, stained with PE-Cy7 anti-mouse CD8a antibody (Clone 53-6.7, BD Biosciences, San Jose, CA, USA cat #552877) and analyzed for the proliferation of T cells stained by quantifying CellTrace violet proliferation peaks using flow cytometry.

Transgenic Assay:

Article Title: Cathepsin S Regulates Antigen Processing and T Cell Activity in Non-Hodgkin Lymphoma.
Article Snippet: At the end of the B cell/T cell co-culture, cells were collected, stained with PE-Cy7 anti-mouse CD8a antibody (Clone 53-6.7, BD Biosciences, San Jose, CA, USA cat #552877) and analyzed for the proliferation of T cells stained by quantifying CellTrace violet proliferation peaks using flow cytometry.



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