Streptavidin Iron Oxide Nanoparticles

SKU:BHD12200115
Overview
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Streptavidin-conjugated superparamagnetic iron oxide nanoparticles (10–30 nm). Streptavidin surface binding captures biotinylated antibodies, nucleic acids, and other biotinylated ligands. Applied to biotin–streptavidin magnetic capture, nucleic acid isolation, and magnetic immunoassay development.
Particle Type Iron Oxide Nanoparticle
Surface Chemistry Streptavidin
Particle Size 10 nm–10 nm, 20 nm and 30 nm
Conjugation Type Pre-conjugated
Dispersion Aqueous
Applications Immunoassay, Nucleic Acid Isolation, Cell Separation
Options selector
Catalog no. Particle Size Volume
SHS10-01 10 nm
SHS20-01 20 nm
SHS30-01 30 nm
Combo-SHS-3 10 nm, 20 nm and 30 nm
Available Options

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

  • Options: Particle Size (4 options): 10 nm, 10 nm, 20 nm and 30 nm, 20 nm, 30 nm | Volume (3 options): 1 mL, 3 x 1 mL, 5 mL
  • Lead time: varies by selected option; please contact us for current fulfillment timing.
  • Storage: Store at 2-8°C.
  • Shipping: cold-chain shipment (typically with ice packs).
  • 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 SHS10, SHS20, SHS30, Combo-SHS-3
Concentration 1 mg/mL
Form solid
Molecular Weight 231.53 g/mol
Product Type
  • Beads & Nanoparticles
  • Nanoparticles
  • Iron Oxide Nanoparticles
Shipping Ice Pack
Storage Store at 2-8°C.

Overview

These Streptavidin Iron Oxide Nanoparticles are superparamagnetic particles with excellent colloidal stability and biocompatible coating for biomedical applications including: in-vivo magnetic resonance imaging (MRI), magnetic particles imaging (MPI), magnetic sensing for in-vitro diagnostics, small molecular drug delivery, immunotherapy, hyperthermia, adjuvant for vaccine, etc. Streptavidin magnetic nanoparticles are nanosized (5-30 nm) iron oxide particles with streptavidin groups. biotinylated nucleic acids, antibodies, or other biotinylated ligands and targets are easily labeled on the iron oxide nanoparticle surface. With excellent colloidal stability and unique surface coating, the streptavidin magnetic nanoparticles exhibit good binding capacity and low non-specific binding of protein or nucleic acids.

Key Features

  • Narrow size distribution
  • High colloidal stability
  • Low non-specific binding
  • Easy conjugation
  • Easy purification with magnetic column developed by Ocean NanoTech

Applications

  • In-vivo magnetic resonance imaging (MRI)
  • Magnetic particles imaging (MPI
  • Magnetic sensing for in-vitro diagnostics
  • Small molecular drug delivery
  • Immunotherapy
  • Hyperthermia
  • Adjuvant for vaccine

Physical & Chemical Properties

  • Zeta Potential: from -10 mV to -30 mV
  • Chemical Stability: The product is chemically stable under standard ambient conditions (room temperature).
  • Incompatible Materials: Strong oxidizing agents
  • Appearance / Color: brown

These are superparamagnetic iron oxide nanoparticles (10–30 nm, 10 mg/mL) with streptavidin conjugated to their surface. Streptavidin binds biotin with extremely high affinity (Kd ≈ 10⁻¹⁵ M), enabling fast and essentially irreversible capture of any biotinylated molecule — including antibodies, oligonucleotides, proteins, and small molecules — under mild aqueous conditions.

Nanoparticle-streptavidin (10–30 nm) provides much larger surface area per mg than micron-sized beads and longer suspension time, maximizing contact with dilute biotinylated targets in solution-phase capture. They are suited for assays where fast diffusion-driven binding is important.

Applications include biotin–streptavidin magnetic capture of biotinylated antibodies, nucleic acids, proteins, and cells; nucleic acid isolation using biotinylated probes; magnetic immunoassay development; and target cell depletion or enrichment.

Available in 10, 20, and 30 nm particle sizes, and in 1 mL and 5 mL volumes. A combo pack of all three sizes is available for comparative experiments.

Store at 2–8°C. Do not freeze. Bath-sonicate before use to ensure complete resuspension. Avoid amine-containing buffers (Tris, glycine) during incubation steps as free amines can compete with biotin binding at high concentrations.

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. 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
  3. 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
  4. Liu X et al. (2026). Interacting proteins of AMPK studied using TurboID proximity labeling technology. Exp Ther Med. DOI: 10.3892/etm.2026.13144 PMID: 42022757
  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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