RY(ham) Yoshida Sarcoma cell

What it means: Species tells you which organism this cell line originates from. Here, Rat indicates the cells were derived from Rat tissue.

Why it matters:

• Biological relevance: Species affects how well the model reflects the biology you want to study and which pathways or receptors are present.
• Reagent & assay compatibility: Antibody reactivity, primers/probes, reference genomes, and detection kits often need to match the species.
• Data interpretation: Baseline gene expression and drug response can differ across species, so controls and conclusions should be species-appropriate.

How to interpret here: The Rat value confirms the species background for this line. Pair it with species-matched controls and verify cell identity/QC (e.g., authentication and mycoplasma testing) in your workflow.

What it means: Disease model describes the disease context the cell line is derived from or commonly used to study. Here, Sarcoma indicates relevance to Sarcoma-related biology.

Why it matters:

• Fit-for-purpose: Disease-associated lines may retain phenotypes that are useful for mechanism studies, biomarker work, or target validation.
• Screening context: Disease background can influence pathway activity and treatment response, which affects assay sensitivity and hit interpretation.
• Controls: Comparing to matched “normal” or tissue-matched controls helps separate disease effects from cell-type effects.

How to interpret here: Use Sarcoma as a guide for whether this model fits your hypothesis. Phenotypes can drift with passage, so keep passage windows consistent and confirm key markers for your use case when possible.

What it means: Growth Properties describes how the cells grow in culture—such as whether they attach to the surface (adherent), grow free-floating (suspension), or show mixed behavior. Here, Adherent,suspension summarizes the expected growth pattern.

Why it matters:

• Culture setup: Growth mode determines vessel choice, coating needs, and whether you culture as a monolayer or in suspension.
• Passaging & counting: Adherent vs suspension growth changes dissociation, viability assessment, and how you calculate seeding density.
• Assay compatibility: Some workflows (imaging, barrier assays) prefer adherent monolayers, while others (bioreactors, some screens) are easier in suspension.

How to interpret here: Use Adherent,suspension to plan your routine culture workflow and assay format.

• Adherent culture: Plan for coated/uncoated plastic as recommended, gentle dissociation, and confluence-based passaging.
• Suspension culture: Use appropriate agitation/handling, monitor clumping, and count cells with methods suited to suspension growth.