Mouse CD19+ B Cells

SKU:BHC18500283
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iXCells Biotechnologies
iXCells Biotechnologies
Details Products
Overview
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Mouse immune cells and hematopoietic cells for in vitro research and model development. Key attributes: Primary Cells, Custom Cells; Cryopreserved; Inquire about custom lot sizes, package sizes and marker characterization; BSL-1. Commonly used in Blood biology workflows (assay dependent).
Species Mouse
Cell Type Immune Cells AND Hematopoietic Cells
Tissue Details CD19+ B
Breed/Strain CD1
Disease Normal
Options selector
Catalog no. Form Size
10MU-016 Cryopreserved
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Form: Cryopreserved; Size: Inquire about custom lot sizes, package sizes and marker characterization
  • Storage: Liquid nitrogen
  • Shipping: cold-chain shipment on dry ice.
  • Upon receipt: transfer to liquid nitrogen storage as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Species Mouse
Applications
  • Cell Culture (Growth)
  • Immunophenotyping
  • Flow Cytometry
Cell type Immune Cells AND Hematopoietic Cells
Classification Primary Cells, Custom Cells
Disease Normal
Biosafety level BSL-1
Storage Liquid nitrogen
Shipping Dry ice
Catalog no. (Mfr.) 10MU-016
Main SKU BHC18500283

Overview

Mouse CD19+ B Cells is a cell model used for research applications where physiologically relevant identity and donor background support interpretation of experimental readouts. Mouse Immune Cells AND Hematopoietic Cells within the Blood system.

*** Product available by custom isolation only, please contact us to get a quote. ***

Key elements and design rationale

  • Cell identity: Immune Cells AND Hematopoietic Cells (Primary Cells, Custom Cells)
  • Source context: CD19+ B; Blood
  • Biosafety level: BSL-1 (follow your institution’s biosafety program and local regulations)

Product-specific elements (such as tissue source, donor background, and cell classification) help frame how results should be interpreted across assays and experimental conditions.

Biological background

Cells originating from the Blood system are commonly studied to understand tissue-specific physiology, signaling, and responses to perturbations in controlled in vitro settings.

Across primary and specialty cell models, experimental outcomes can be influenced by donor heterogeneity, passage history, confluence, and media composition. For interpretation, it is common to validate key markers or functional phenotypes in the user’s assay context and to document culture variables consistently.

Research relevance and current trends

  • Increasing use of primary and specialty cells to improve translational relevance for target biology and phenotypic screening.
  • Adoption of 3D culture formats and co-culture systems to better capture tissue microenvironments and cell–cell interactions.
  • Integration of functional readouts with single-cell and multi-omics profiling to connect phenotype with molecular state.
  • Expansion of high-dimensional immune phenotyping and perturbation screens to map activation states and functional programs.

Common research applications

  • Profile identity markers by flow cytometry or immunostaining in cultured cells
  • Stimulate immune cells and quantify activation markers and cytokine release
  • Quantify functional responses to defined stimuli relevant to the model system
  • Compare baseline phenotype across donors/conditions using gene expression profiling
  • Perform immune profiling by multiparameter flow cytometry to resolve major subsets

Interpretation typically focuses on how a perturbation (e.g., cytokine exposure, metabolic stress, genetic manipulation, or compound treatment) shifts marker profiles or functional readouts relative to an appropriate control matched for donor and culture variables.

Notes for experimental interpretation

  • Donor-to-donor heterogeneity can influence baseline phenotype and treatment response; include biological replicates when feasible.
  • Passage number, confluence, and media composition can shift gene expression and functional readouts; track and report these variables consistently.
  • Contamination control (including routine mycoplasma monitoring) supports reproducibility in downstream assays.
  • Use appropriate negative/positive controls for the readout (e.g., unstimulated controls, pathway agonists/antagonists) to contextualize observed changes.

SKU:BHC18500283

Customization & Add-ons: Can't find the cell line you need—or require a custom cell-based solution for your project? We can help you source the best match or support custom cell line services for diverse research needs, including cell line sourcing and selection (species, tissue, and disease model matching), stable cell line engineering (overexpression, knockdown, or knockout via CRISPR/Cas9, shRNA, or sgRNA), reporter gene integration (GFP, RFP, luciferase, and other fluorescent or bioluminescent constructs), genome editing and knockin (point mutations, tagged endogenous proteins, conditional alleles), inducible expression systems (Tet-On/Off and other regulatable constructs), drug resistance marker selection (puromycin, G418, hygromycin, and others), custom growth and media optimisation for specific assay requirements, scale-up production for high-throughput screening campaigns, and authentication and QC services (STR profiling, mycoplasma testing, viability assessment). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.

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