CD45 iFluor™ 700

SKU:BHA19900451
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    Overview
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    Anti-CD45 antibody from Mouse Monoclonal, clone F10-89-4 isotype IgG2a, k conjugated to iFluor™ 700 reactive with Human for FC applications. Commonly used in immunology & inflammation studies, including workflows such as flow cytometry.
    Target CD45
    Clone number F10-89-4
    Host Mouse
    Reactivity Human
    Isotype IgG2a, k
    Conjugate(s) iFluor™ 700
    Application(s) FC
    Excitation Laser Red (633nm)
    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
    1016194 25 Tests
    1016195 100 Tests
    1016196 200 Tests
    Field Specification
    Clonality
    • Monoclonal
    Conjugate
    • iFluor™ 700
    Host Mouse
    Immunogen Human T lymphocytes
    Isotype
    • IgG2a
    • k
    Product Type
    • Antibodies
    • Primary Antibodies
    • Flow Cytometry Antibodies
    Reactivity
    • Human
    Storage 2-8°C
    Target CD45

    Overview

    CD45 iFluor™ 700 is a Mouse monoclonal targeting CD45, supplied as a iFluor™ 700 format for FC workflows. It supports measurement of Human target expression in common experimental systems.

    Key elements and design rationale

    • Clone: F10-89-4 — consistent clone identity can support panel reproducibility and cross-study comparisons.
    • Isotype: IgG2a, k — informs selection of matched controls and secondary reagents when relevant.
    • Conjugate: iFluor™ 700 — enables direct detection in fluorescence-based assays. Excitation is typically matched to Red (633nm) 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 F10-89-4, a mouse monoclonal antibody, recognizes a hematopoietic cell surface antigen known as CD45 which is present on all human leukocytes including lymphocytes, monocytes, granulocytes, eosinophils, and basophils in peripheral blood. CD45 has a role in signal transduction, modifying signals from other surface molecules. The CD45 antibody has been reported to react weakly with mature circulating erythrocytes and platelets. The antibody recognizes the human leukocyte common antigen which is found on cells from spleen, lymph nodes, 83% bone marrow cells, and granulocytes. The antigen recognized by F10-89-4 is a glycoprotein with a molecular weight of 190 kDa to 215 kDa.

    Research relevance and current trends

    • High-parameter immunophenotyping: combining CD45 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 CD45-positive populations and compare expression distributions across conditions or time points.
    • Cell sorting: enrich CD45-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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