CD10 FITC

SKU:BHA19900030
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    Overview
    Click light‑blue chips for details
    Anti-CD10 antibody from Mouse Monoclonal, clone C-1A12 isotype IgG1, k conjugated to FITC reactive with Human for FC applications. Commonly used in immunology & inflammation studies, including workflows such as flow cytometry.
    Target CD10
    Clone number C-1A12
    Host Mouse
    Reactivity Human
    Isotype IgG1, k
    Conjugate(s) FITC
    Application(s) FC
    Excitation Laser Blue (488nm)
    Available Options

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

    • Options: Size (3) - 25 Tests, 100 Tests, 200 Tests
    • Lead time: typically ships in ~2-3 business days; timing may vary by selected option.
    • Storage: 2-8°C
    • Shipping: cold-chain shipment (typically with ice packs).
    • Upon receipt: refrigerate upon receipt.
    • Sales terms and conditions: Please review prior to ordering.
    Options selector
    Catalog no. Size
    114914 25 Tests
    114915 100 Tests
    114916 200 Tests
    Field Specification
    Clonality
    • Monoclonal
    Conjugate
    • FITC
    Host Mouse
    Isotype
    • IgG1
    • k
    Product Type
    • Antibodies
    • Primary Antibodies
    • Flow Cytometry Antibodies
    Reactivity
    • Human
    Storage 2-8°C
    Target CD10

    Overview

    CD10 FITC is a Mouse monoclonal targeting CD10, supplied as a FITC format for FC workflows. It supports measurement of Human target expression in common experimental systems.

    Key elements and design rationale

    • Clone: C-1A12 — consistent clone identity can support panel reproducibility and cross-study comparisons.
    • Isotype: IgG1, k — informs selection of matched controls and secondary reagents when relevant.
    • Conjugate: FITC — enables direct detection in fluorescence-based assays. Excitation is typically matched to Blue (488nm) lasers in cytometer configurations.
    • Host species: Mouse — useful for panel design and control strategy planning.
    • Reactivity: Human — interpret staining in the context of species-specific sequence and expression differences.

    Key specifications such as clone identity, isotype, and fluorophore conjugation help researchers align panel design, control selection, and instrument configuration with the biological question and sample type.

    Biological background

    The clone C-1A12, a mouse monoclonal antibody recognizes a 100 kDa protein that has neutral metalloendopeptidase activity and inactivates a variety of biologically active peptides known as CD10. CD10 is type II transmembrane glycoprotein and a common acute lymphocytic leukemia antigen that is an important cell surface marker in the classification of human acute lymphocytic leukemia (ALL). The protein is present on leukemic cells of pre-B phenotype, which represent 85% of cases of ALL. CD10 plays important role in the development process of B cells the in germinal center. This protein is not restricted to leukemic cells. Normal, healthy precursors of B and T cells and granulocytes also express CD10.

    Research relevance and current trends

    • High-parameter immunophenotyping: combining CD10 with complementary lineage and activation markers to resolve complex cell states.
    • Panel standardization and data comparability: increasing emphasis on consistent reagents, compensation-aware fluorophore choices, and shared gating strategies.
    • Integration with single-cell multi-omics: pairing surface marker profiling with transcriptomic or proteomic readouts to connect phenotype to function.

    Common research applications

    • Flow cytometry: quantify CD10-positive populations and compare expression distributions across conditions or time points.
    • Cell sorting: enrich CD10-defined subsets for downstream RNA/protein assays or functional readouts.

    Changes in measured signal are typically interpreted in the context of cell subset frequency, activation/differentiation state, and sample processing effects rather than as a standalone readout.

    Notes for experimental interpretation

    • Fluorophore selection: consider brightness, spectral overlap, and instrument configuration; compensation and spillover can affect apparent population boundaries.
    • Biology-driven confounders: activation state, differentiation, and isoform/PTM variation can shift epitope accessibility and apparent expression.
    • Control concepts: include matched isotype and fluorescence-minus-one (FMO) controls where appropriate, and interpret results alongside biological positive/negative reference samples.

    For antibody-based assays, monoclonal versus polyclonal format can influence epitope recognition breadth and signal consistency. Conjugated antibodies support direct detection and can simplify multicolor panel design when paired with appropriate controls and instrument settings.

    Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). 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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