SMURF2 Antibody

SKU:BHA17128068
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NSJ Bioreagents
NSJ Bioreagents
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Overview
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Anti-SMURF2 antibody from Mouse (clone 1826CT865.51.28) unconjugated. Designed for target detection, including Western blotting; for Human samples. Commonly used in workflows such as Western blotting.
Target SMURF2
Clone Number 1826CT865.51.28
Conjugate(s) Unconjugated
Host Mouse
Reactivity Human
Application WB
Options selector
Catalog no. Formulation Size
F54130-0.05ML In 1X PBS, pH 7.4, with 0.09% sodium azide
Available Options

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

  • Options: Formulation: In 1X PBS, pH 7.4, with 0.09% sodium azide; Size (2) - 0.2 ml, 0.05 ml
  • Lead time: typically ships in ~2-3 business days; timing may vary by selected option.
  • Storage: Aliquot the SMURF2 antibody and store frozen at -20˚C or colder. Avoid repeated freeze-thaw cycles.
  • 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 F54130
Clonality
  • Monoclonal (mouse origin)
Host Mouse
Immunogen Recombinant human SMURF2 was used as the immunogen for the SMURF2 antibody.
Isotype
  • Mouse IgG1
  • kappa
Product Type
  • Antibodies
  • Primary Antibodies
Purity Protein G purified
Reactivity
  • Human
Storage Aliquot the SMURF2 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Target SMURF2
UniProt # Q9HAU4

Overview

SMURF2 Antibody is an antibody targeting SMURF2, raised in Mouse for protein detection and localization studies where these specifications are required.

Key elements and design rationale

  • Target: SMURF2.
  • Antibody identity: Monoclonal (mouse origin); Clone 1826CT865.51.28; Mouse IgG1, kappa.
  • Conjugate/label: Unconjugated (affects detection chemistry and multiplex compatibility).
  • Format: Purified.
  • Species reactivity: Human.
  • Listed applications: WB (refer to on-page specifications for application-specific guidance).

Biological background

E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Interacts with SMAD1 and SMAD7 in order to trigger their ubiquitination and proteasome-dependent degradation. In addition, interaction with SMAD7 activates autocatalytic degradation, which is prevented by interaction with SCYE1. Forms a stable complex with the TGF-beta receptor-mediated phosphorylated SMAD2 and SMAD3. In this way, SMAD2 may recruit substrates, such as SNON, for ubiquitin-mediated degradation. Enhances the inhibitory activity of SMAD7 and reduces the transcriptional activity of SMAD2. Coexpression of SMURF2 with SMAD1 results in considerable decrease in steady-state level of SMAD1 protein and a smaller decrease of SMAD2 level. [UniProt]

Research relevance and current trends

  • Comparative expression profiling across cell types, tissues, or perturbations (e.g., drug treatment, genetic editing, or differentiation).
  • Subcellular localization and trafficking studies, including co-localization with pathway markers in microscopy-based assays.
  • Integration of protein-level measurements with transcriptomics or proteomics to relate abundance to regulation and phenotype.

Common research applications

  • Western blotting: researchers commonly compare relative signal levels across conditions and use appropriate negative/positive controls for interpretation.

Interpretation should account for antibody-dependent factors such as epitope accessibility, isoforms, and sample preparation differences across workflows.

Notes for experimental interpretation

  • Isoforms and PTMs: many targets have multiple isoforms and post-translational modifications that can shift apparent signal or localization; interpret bands/signals accordingly.
  • Epitope context: binding can depend on protein conformation and sample processing; region information in the title/immunogen can help anticipate what may be detected.
  • Species differences: predicted or validated reactivity may vary by ortholog sequence and sample context; confirm in your model system.
  • Control concepts: include negative controls (no-primary/isotype), and where possible genetic controls (KO/KD) or independent antibodies to strengthen conclusions.

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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