CYBB Antibody / NOX2 / gp91phox

SKU:BHA17109822
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NSJ Bioreagents
NSJ Bioreagents
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Overview
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Anti-CYBB antibody (Rabbit, clone GOH-3, Rabbit IgG) for WB in research assays (RUO).
Target CYBB
Clone number GOH-3
Host Rabbit
Reactivity Human
Isotype Rabbit IgG
Application WB
Conjugate(s) Unconjugated
Options selector
Catalog no. Formulation Size
RQ5084 Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5mg/ml BSA
Available Options

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

  • Options: Formulation: Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5mg/ml BSA; Size: 100 ul
  • Lead time: typically ships in ~2-3 business days; timing may vary by selected option.
  • Storage: Store the CYBB antibody at -20oC.
  • 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 RQ5084
Clonality
  • Rabbit Monoclonal
Host Rabbit
Immunogen A synthetic peptide specific to human Nox2 / CYBB was used as the immunogen for the CYBB antibody.
Isotype
  • Rabbit IgG
Product Type
  • Antibodies
  • Primary Antibodies
Purity Affinity purified
Reactivity
  • Human
Storage Store the CYBB antibody at -20oC.
Target CYBB
UniProt # P04839

Overview

CYBB Antibody / NOX2 / gp91phox is a research-use antibody directed against CYBB. It is supplied for use in common immunoassay contexts such as WB (RUO).

Key elements and design rationale

  • Target: CYBB.
  • Description (provided): Critical component of the membrane-bound oxidase of phagocytes that generates superoxide.
  • Antibody type: Rabbit, clone GOH-3, Rabbit IgG.
  • Format: Purified; Affinity purified.
  • Species reactivity: tested: Human.
  • Immunogen (if provided): A synthetic peptide specific to human Nox2 / CYBB was used as the immunogen for the CYBB antibody..

The information above helps you match the antibody format to your assay context, interpret species-dependent differences, and anticipate how epitope context (isoforms, PTMs, or conformational state) may influence signal.

Biological background

Critical component of the membrane-bound oxidase of phagocytes that generates superoxide. It is the terminal component of a respiratory chain that transfers single electrons from cytoplasmic NADPH across the plasma membrane to molecular oxygen on the exterior. Also functions as a voltage-gated proton channel that mediates the H+ currents of resting phagocytes. It participates in the regulation of cellular pH and is blocked by zinc. [UniProt]

For curated annotations (gene/protein naming, domains, isoforms, and pathway links) for CYBB, consult primary databases such as UniProt, NCBI Gene, and Ensembl.

Research relevance and current trends

  • Context-dependent expression studies: researchers often examine CYBB abundance and localization across perturbations (genetic, pharmacologic, or environmental) to connect phenotype to molecular changes.
  • Reagent reproducibility: there is growing emphasis on antibody specificity checks using orthogonal approaches (e.g., genetic perturbation or independent antibodies) and transparent reporting of clone/lot information.
  • Multi-modal datasets: antibody-based readouts are increasingly combined with transcriptomics and imaging to relate protein-level measurements to cell-state transitions.

Common research applications

  • Western blotting (immunoblot) for relative detection of target protein abundance and apparent molecular weight.

When comparing conditions, interpret changes in signal in the context of sample composition, expected localization, and any known isoform complexity for the target.

Notes for experimental interpretation

  • Isoforms and PTMs: alternative splicing or post-translational modifications can change epitope accessibility and apparent molecular weight; interpret bands/signals accordingly.
  • Cross-reactivity and matrix effects: background binding can vary by sample type, species, and blocking/detection chemistries; include appropriate negative controls.
  • Control concepts: where feasible, use genetic perturbation (KO/KD/overexpression), orthogonal assays, or independent antibodies to support specificity claims.

Antibody considerations: Polyclonal reagents may recognize multiple epitopes and can increase sensitivity but may show broader binding profiles, while monoclonal clones provide a single-epitope readout that can improve consistency across experiments. If a conjugate is listed, the antibody supports more direct detection workflows; otherwise, it is typically used with a compatible secondary antibody.

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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