HLA-B Antibody

SKU:BHA17112207
Suppliers
NSJ Bioreagents
NSJ Bioreagents
Details Products
Overview
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Research-use anti-HLA-B primary antibody (Mouse, clone EP-4, isotype Mouse IgM, kappa) for FACS, IF and related target-detection assays in RUO workflows.
Target HLA-B
Clone number EP-4
Host Mouse
Reactivity Human
Conjugate(s) Unconjugated
Application FACS, IF
Options selector
Catalog no. Formulation Size
V2577-100UG 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide
V2577SAF-100UG 1 mg/ml in 1X PBS; BSA free, sodium azide free
Available Options

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

  • Options: Formulation (2) - 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide, 1 mg/ml in 1X PBS; BSA free, sodium azide free; Size (2) - 100 ug, 20 ug
  • Lead time: typically ships in ~2–3 business days; timing may vary by selected option.
  • Storage: Store the HLA-B antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No V2577
Clonality
  • Monoclonal (mouse origin)
Host Mouse
Immunogen Lymphocytes from an HLA-B27 patient were used as the immunogen for the HLA-B antibody.
Isotype
  • Mouse IgM
  • kappa
Product Type
  • Antibodies
  • Primary Antibodies
Purity PEG precipitation
Reactivity
  • Human
Storage Store the HLA-B antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
Target HLA-B
UniProt # P03989

Overview

HLA-B Antibody is a research-use primary antibody intended for detection of HLA-B in experimental workflows. It is supplied in Purified format. Key antibody attributes include Mouse, Monoclonal (mouse origin), clone EP-4, isotype Mouse IgM, kappa. Applications listed for this product include FACS, IF. Reported/annotated localization context: Cell surface. Species reactivity (as provided): Human.

Key elements and design rationale

  • Target: HLA-B — selectivity and interpretation should be considered in the context of isoforms, post-translational modifications, and related family members when applicable.
  • Format: Purified — format can influence background, multiplexing compatibility, and downstream detection strategies.
  • Antibody identity: Mouse, Monoclonal (mouse origin), clone EP-4, isotype Mouse IgM, kappa — these attributes help align secondary reagents and controls (e.g., isotype-matched controls) with your assay design.
  • Localization: Cell surface — expected subcellular distribution can guide band/structure interpretation and help flag off-target signal.
  • Product notes (from provided description): This mAb recognizes the HLA-B27 cell surface antigen on human cells. It may be used to HLA type human lymphocytes. Approximately 60% of patients with ankylosing spondylitis are HLA-B27 positive. This reagent can be used to help identify this HLA haplotype in human lymphocytes. Major histocompatibility complex (MHC) molecules form an integral part of the immune response system. They are cell-surface receptors that bind pep- tides and present them to T lymphocytes. Human leukocyte antigens (HLAs) are polymorphic members of the MHC family that are specifically involved in the presentation of antigens to the T cell receptor. There are two classes of HLA antigens: class I (HLA-A, HLA-B and HLA-C) and class II (HLA-D). Class I molecules are expressed in nearly all cells and play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum. The differential structural properties of MHC class I and class II molecules account for their respective roles in activating different populations of T lymphocytes. HLA-B encodes a membrane anchored heavy chain, which hetero-dimerizes with a light chain (b-2-Microglobulin) to form MHC-I. Polymorphisms yield hundreds of HLA-B alleles. The HLA-B27 allele appears with increased frequency in uveitis patients.

Where multiple assay formats are possible, align the antibody format, host/isotype, and listed applications with your detection system and controls to support clear interpretation of signal.

Biological background

In this catalog, HLA-B is positioned within Immunology & Inflammation research contexts. Localization annotations (e.g., Cell surface) can help contextualize expected signal patterns in imaging and fractionation-based readouts. For authoritative gene/protein nomenclature, domains/isoforms, and curated functional annotations, consult resources such as UniProt, NCBI Gene, and Ensembl.

Research relevance and current trends

  • Higher-plex and spatially resolved readouts (e.g., multiplex IF/IHC, spatial omics) are increasing demand for well-characterized primary antibodies with clearly stated host/isotype and labeling strategies.
  • Genetic perturbation controls (knockout/knockdown) and orthogonal measurements (e.g., RNA vs protein) are commonly used to strengthen target attribution when interpreting antibody-derived signals.
  • Reproducibility initiatives emphasize transparent reporting of antibody identity (clone, host, isotype) and experimental context to improve cross-study comparability.

Common research applications

  • FACS: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
  • IF: interpret changes in signal in the context of sample composition, epitope accessibility, and potential isoform/PTM differences across conditions.
  • Typical workflow themes: IF/ICC localization, Flow cytometry staining, ELISA binding assay, Specificity controls.
  • Workflow notes: Detect HLA-B localization by IF/ICC in cultured cells (optimize fixation + dilution), Quantify HLA-B-positive cells by flow cytometry in single-cell suspensions (include viability gate), Measure binding to HLA-B pepti…

When comparing conditions, consistent sample processing and appropriate negative/positive controls support interpretation of qualitative localization differences and quantitative abundance changes.

Notes for experimental interpretation

  • Isoforms and post-translational modifications may shift apparent molecular weight or epitope accessibility, especially across cell states or treatments.
  • Species and tissue context can affect sequence conservation, expression level, and background binding; predicted reactivity should be verified in your sample.
  • Control concepts include isotype-matched controls, secondary-only controls (for indirect detection), and genetic/orthogonal controls (e.g., KO/KD, independent antibodies, or RNA measurements) when feasible.

Monoclonal and polyclonal antibodies can differ in epitope recognition breadth and lot-to-lot characteristics; consider clonality and clone information (when provided) alongside your assay requirements. Conjugated formats may simplify detection but can change background and multiplexing behavior compared with unconjugated primaries.

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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