CD45 mFluor500

SKU:BHA19900448
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Overview
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Anti-CD45 antibody from Mouse Monoclonal, clone F10-89-4 isotype IgG2a, k conjugated to mFluor™ 500 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) mFluor™ 500
Application(s) FC
Excitation Laser Violet (405nm)
Options selector
Catalog no. Size
1016154 25 Tests
1016155 100 Tests
1016156 200 Tests
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.
Field Specification
Mfr No 1016154; 1016155; 1016156
Clonality
  • Monoclonal
Conjugate
  • mFluor™ 500
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 mFluor500 is a Mouse monoclonal targeting CD45, supplied as a mFluor™ 500 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: mFluor™ 500 — enables direct detection in fluorescence-based assays. Excitation is typically matched to Violet (405nm) 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 CD45 antigen is present on all human leucocytes including lymphocytes, monocytes, granulocytes, eosinophils, and basophils in peripheral blood. The antigen has a role in signal transduction, modifying signals from other surface molecules. The CD45 has been reported to react weakly with mature circulating erythrocytes and plateletsThe 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 190kDa to 215kDa.

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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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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