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Polystyrene beads with Amine Groups (20 nm) Conjugates Molecular Depot
Polystyrene beads with Amine Groups (20 nm) Conjugates Molecular Depot
Polystyrene beads with Amine Groups (20 nm) Conjugates Molecular Depot
Polystyrene beads with Amine Groups (20 nm) Conjugates Molecular Depot

Polystyrene beads with Amine Groups (20 nm)

$1,295.00

    Catalog Number: B2013396 (1 ml)

    Polystyrene beads with Amine Groups (20 nm) are amine-functionalized 20 nm polystyrene nanoparticles supplied as a 1 mL suspension. The surface amine groups enable easy covalent conjugation of proteins, antibodies, dyes, or drugs using standard EDC/NHS chemistry. These beads are ideal for creating custom targeted nanoparticles, diagnostic assays, cellular uptake studies, and surface chemistry research. Custom bulk amounts of this product are available upon request.

    Products are for in vitro research use only (RUO).

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Polystyrene Beads with Amine Groups (20 nm) – Catalog #B2013396

Polystyrene Beads with Amine Groups (20 nm) (Catalog #B2013396) are uniform 20 nm polystyrene nanoparticles bearing surface amine (-NH₂) functional groups, supplied as a 1 mL aqueous suspension. The primary amine groups enable straightforward covalent conjugation to carboxyl-containing molecules, proteins, antibodies, dyes, or other ligands using standard EDC/NHS chemistry. These aminated beads are excellent tools for creating custom functionalized nanoparticles, targeted drug delivery systems, diagnostic assays, and surface chemistry studies.

Catalog number: B2013396
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 mL
Molecular Weight or Concentration: N/A (particle suspension)
Supplied as: Aqueous suspension
Applications: Covalent bioconjugation, targeted nanoparticle preparation, immunoassay development, drug delivery research, cell labeling, and surface functionalization studies
Storage: 2-8°C (do not freeze)
Keywords: Polystyrene beads Aminated, amine-functionalized polystyrene nanoparticles, 20 nm NH2 beads
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

Scientific Overview

These 20 nm amine-functionalized polystyrene beads provide reactive primary amine groups on the surface for easy covalent attachment of biomolecules via EDC/NHS coupling or other amine-reactive chemistries. The small size combined with high surface area makes them ideal for creating targeted nanoconjugates, fluorescent probes, drug-delivery vehicles, and diagnostic reagents. They are widely used in nanomedicine, immunoassay development, cell labeling, and fundamental studies of nanoparticle–cell interactions.

Key applications include:

  • Covalent conjugation of antibodies, proteins, peptides, or dyes
  • Development of targeted nanoparticles for drug delivery
  • Immunoassays and lateral flow diagnostics
  • Cellular uptake and intracellular trafficking studies
  • Fluorescent labeling and imaging probes

Usage & Handling Guidance

Store at 2–8°C. Do not freeze. Gently vortex or pipette up and down before use to ensure uniform suspension. For conjugation, wash beads if necessary and follow standard EDC/NHS protocols. After conjugation, blocking with glycine or ethanolamine is recommended to quench unreacted groups.

  • Typical working concentration: 0.1–1% (w/v) for conjugation reactions
  • Conjugation chemistry: EDC/NHS for carboxyl-containing ligands
  • Stability: Stable for months when stored refrigerated; protect from contamination

What You Get

  • 1 mL of 20 nm Polystyrene Beads with Amine Groups (aqueous suspension)
  • Reactive surface amine groups for covalent bioconjugation
  • Uniform particle size and high surface area
  • Ready for direct use in coupling reactions
  • For research use only (RUO)

Why Researchers Choose It

  • Ready-to-conjugate amine surface for easy attachment of biomolecules
  • Small 20 nm size ideal for nanomedicine and cellular uptake studies
  • Stable, high-quality polystyrene core with low non-specific binding
  • Versatile platform for creating custom fluorescent or targeted nanoparticles
  • Convenient suspension format for immediate experimental use

Frequently Asked Questions (FAQ)

  • What chemistry can be used for conjugation?
    Standard EDC/NHS coupling to carboxyl groups is most common. Other amine-reactive reagents (e.g., NHS-esters) can also be used.
  • Can these beads be used in live cells?
    Yes. They are suitable for cellular uptake, trafficking, and nanomedicine studies after conjugation.
  • How should I store the product?
    Store at 2–8°C. Do not freeze. Mix gently before use.
  • What is the concentration?
    The suspension is typically used as supplied or diluted according to your conjugation protocol.
  • Are the beads fluorescent?
    No. These are plain aminated polystyrene beads. Fluorescent versions (e.g., FITC, Cy5) are available separately.
This product is for Research Use Only (RUO). It is not intended for diagnostic or therapeutic use in humans or animals.

References

  • Kiremitçi M, Pişkin E. Cell adhesion to the surfaces of polymeric beads. Biomater Artif Cells Artif Organs. 1990;18(5):599-603. Reference
  • Townsend JB, Shaheen F, Liu R, Lam KS. Jeffamine derivatized TentaGel beads and poly(dimethylsiloxane) microbead cassettes for ultrahigh-throughput in situ releasable solution-phase cell-based screening of one-bead-one-compound combinatorial small molecule libraries. J Comb Chem. 2010 Sep 13;12(5):700-12. Reference
  • Tekabe Y, Einstein AJ, Johnson LL, Khaw BA. Targeting very small model lesions pretargeted with bispecific antibody with 99mTc-labeled high-specific radioactivity polymers. Nucl Med Commun. 2010 Apr;31(4):320-7. Reference
  • Zhang Y, McElrea A, Sanchez GV Jr, Do D, Gomez A, Aguirre SL, Rendy R, Klumpp DA. Dicationic electrophiles from olefinic amines in superacid. J Org Chem. 2003 Jun 27;68(13):5119-22. Reference
  • Jain R, Agarwal A, Kierski PR, Schurr MJ, Murphy CJ, McAnulty JF, Abbott NL. The use of native chemical functional groups presented by wound beds for the covalent attachment of polymeric microcarriers of bioactive factors. Biomaterials. 2013 Jan;34(2):340-52. Reference
  • Rose SL, Babensee JE. Procoagulant phenotype of endothelial cells after coculture with biomaterial-treated blood cells. J Biomed Mater Res A. 2005 Mar 1;72(3):269-78. Reference
  • Byun Y, Jacobs HA, Kim SW. Heparin surface immobilization through hydrophilic spacers: thrombin and antithrombin III binding kinetics. J Biomater Sci Polym Ed. 1994;6(1):1-13. Reference
  • You JB, Yoo Y, Oh MS, Im SG. Simple and reliable method to incorporate the Janus property onto arbitrary porous substrates. ACS Appl Mater Interfaces. 2014 Mar 26;6(6):4005-10. Reference
  • Cho WS, Duffin R, Poland CA, Howie SE, MacNee W, Bradley M, Megson IL, Donaldson K. Metal oxide nanoparticles induce unique inflammatory footprints in the lung: important implications for nanoparticle testing. Environ Health Perspect. 2010 Dec;118(12):1699-706. Reference

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Copy of Technical Specifications

FeatureDetails
Viewing Head Siedentopf type trinocular head, inclined at 30°, Interpupillary adjustment 53mm to 75mm, graduated diopter on left eyetube (30mm I.D. eyetubes)
Eyepieces SWH10X Widefield high eyepoint eyepiece, Field No. 22, tube O.D. 30.0 mm
Nosepiece Quintuple
Quintuple LWD Planachromat Phase 10x, 20x
Condenser TC Condenser N.A. 0.30, W.D. 73.0mm
Stage180mm(X) x 245mm(Y) plain stage with replaceable glass insert with 45mm opening, Glass Stage plate insert
IlluminationKoehler without iris, with phase slider, 3W LED
WarrantyLIMITED LIFETIME WARRANTY

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