Protein G Iron Oxide Nanoparticles

SKU:BHD12200274
Suppliers
Ocean NanoTech, LLC
Ocean NanoTech, LLC
Details Products
Overview
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Protein G-conjugated superparamagnetic iron oxide nanoparticles (10–30 nm) for antibody capture via Fc-region binding. Applied to immunoprecipitation, antibody purification, magnetic cell separation, and immunoassay development.
Particle Type Iron Oxide Nanoparticle
Surface Chemistry Protein G
Particle Size 10 nm–30 nm
Conjugation Type Pre-conjugated
Dispersion Aqueous
Applications Immunoassay, Immunoprecipitation, Cell Separation
Options selector
Catalog no. Particle Size Volume
IPG10-01 10 nm
IPG30-01 30 nm
Available Options

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

  • Options: Particle Size (2 options): 10 nm, 30 nm | Volume (2 options): 1 mL, 5 mL
  • Lead time: varies by selected option; please contact us for current fulfillment timing.
  • Storage: Refer to the product datasheet for storage and handling.
  • Shipping: see shipping details at checkout.
  • Upon receipt: inspect packaging; record lot number; allow product to reach appropriate working temperature per the product datasheet before use.
  • Sales terms and conditions: all sales are subject to BioHippo's standard Terms and Conditions.
Field Specification
Mfr No IPS10, IPS30, IPG10, IPG30
Product Type
  • Beads & Nanoparticles
  • Nanoparticles
  • Iron Oxide Nanoparticles

These are superparamagnetic iron oxide nanoparticles (10–30 nm, 10 mg/mL) with Protein G conjugated to their surface. Protein G binds specifically to the Fc region of IgG antibodies, enabling non-covalent, orientation-controlled antibody immobilization that leaves the antigen-binding (Fab) domains free for target capture.

Protein G binds IgG from human, mouse, rat, rabbit, bovine, goat, and many other species. It shows strong affinity for mouse IgG1 and human IgG3 — subclasses where Protein A affinity is reduced. Check antibody datasheet to confirm Protein G compatibility for your specific isotype.

Applications include immunoprecipitation, co-immunoprecipitation, antibody purification and enrichment from biological fluids, magnetic bead-based immunoassay development, and cell sorting using antibody-loaded nanoparticles.

Apply low-pH elution buffer (e.g., 100 mM glycine, pH 2.0–2.5) and magnetically separate the nanoparticles to recover the eluate. Neutralize the eluate immediately. Protein G binding is reversible, allowing complete antibody recovery under these conditions.

Available in 10 nm and 30 nm particle sizes, in 1 mL and 5 mL volumes per size. Choose 10 nm for maximum surface area; 30 nm for faster magnetic separation.

The following customization and add-on services are available for this product through the supplier. For inquiries and pricing, contact support@biohippo.com.

Customization Options

  • Custom Nanoparticle Synthesis: Iron oxide nanoparticles with customized particle sizes (nanometers to micrometers), narrow size distributions, surface coatings, and functional groups can be synthesized for specialized imaging, drug delivery, or sensing applications.
  • Custom Surface Modification: Deep understanding of surface chemistry allows custom modification of iron oxide nanoparticle surfaces for different applications — including custom PEG lengths, targeting ligands, or specific reactive groups.
  • Custom Conjugation Service: Pre-conjugated iron oxide nanoparticle–antibody, nanoparticle–protein, or nanoparticle–drug conjugates can be prepared using your supplied biomolecule. The supplier specializes in conjugation chemistry across iron oxide nanoparticles, quantum dots, magnetic beads, and latex beads.
  • Assay Development: Technical support for magnetic nanoparticle-based in vitro diagnostic assay development, including magnetic sensing assays and lateral flow platforms, is available.
  • Bulk & OEM Manufacturing: Bulk iron oxide nanoparticle supply and OEM manufacturing for diagnostic and therapeutic research device development are available.

To inquire about customization options, request a quote, or discuss OEM manufacturing, contact support@biohippo.com.

  1. Rezaei E et al. (2026). A deep dive into ferritin nanoparticle advancements: experimental and computational perspectives. Discov Nano. DOI: 10.1186/s11671-026-04577-8 PMID: 42018247
  2. Jensen P et al. (2021). Improved Immunoprecipitation to Mass Spectrometry Method for the Enrichment of Low-Abundant Protein Targets. Methods Mol Biol. DOI: 10.1007/978-1-0716-1186-9_14 PMID: 33420993
  3. Amaolo A et al. (2026). Breaking Through the Barrier: Nanoparticle-Driven MRI Strategies for Diagnosis and Therapy of Pancreatic Cancer. ACS Nanosci Au. DOI: 10.1021/acsnanoscienceau.5c00116 PMID: 42004273
  4. Fan Y et al. (2026). Bio-magnetic nanomedicine for targeted drug delivery of breast cancer: green synthesis, functional design, and translational challenges. Breast Cancer Res. DOI: 10.1186/s13058-026-02278-9 PMID: 42002783
  5. Morais B et al. (2026). Integrating green chemistry into SPION development: a theranostic study on prostate cell models. Nanoscale. DOI: 10.1039/d6nr00113k PMID: 41954586
  6. Dong J et al. (2026). Advancements in nanomaterials for the treatment and management of vascular surgeries: from drug delivery to biomedical implants. Front Bioeng Biotechnol. DOI: 10.3389/fbioe.2026.1788897 PMID: 41953561
  7. Galarza-Arévalo GE et al. (2026). Clinical Applications and Future Prospects of Metallic Nanoparticles in Diagnosis and Therapy. Int J Nanomedicine. DOI: 10.2147/IJN.S567931 PMID: 42023082
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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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