BeaverBeads Mag COOH 300 nm magnetic polymer beads scanning electron micrograph - Figure 1 of 1

Scanning electron micrograph of BeaverBeads Mag COOH polymer microspheres, showing the narrow size distribution characteristic of the monodisperse Mag COOH series. Image published by BEAVER Biomedical Engineering.

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Beaver Biomedical Engineering Co Ltd
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Beaver Biomedical Engineering Co Ltd

BeaverBeads Mag COOH Carboxyl Magnetic Polymer Beads, 300 nm

SKU BHD13200044 · Cat# 70106, 70106-5, 70106-50
In Stock at ManufacturerNew

BeaverBeads Mag COOH-300 are monodisperse 300 nm superparamagnetic polymer beads supplied at 10 mg/mL with approximately 60 umol/g of surface carboxyl groups. EDC/NHS activation couples antibodies, proteins and amine-modified oligonucleotides covalently to the surface for immunoassay development, immunoprecipitation and targeted capture.

At a glance
Particle Type
Magnetic polymer bead
Surface Chemistry
Carboxyl (-COOH)
Mean Particle Size
300 nm, monodisperse
Surface COOH Content
~60 umol/g
Core / Shell
Fe3O4 / polymer
Saturation Magnetisation
46.37 emu/g
Concentration
10 mg/mL
Coupling Chemistry
EDC/NHS to primary amines
See all 3 configurations
All configurations · 3 options
Catalog No.SizeAvailability Price Qty Order
70106-55 mLIn Stock at Manufacturer $1,060.00
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70106-5050 mLIn Stock at Manufacturer $5,460.00
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70106Other size - enquireMade to Order Quote—
Ambient temperature Store at 2-8 C. Do not freeze, dry or centrifuge - all cause irreversible aggregation and loss of surface activity. Shipping calculated at checkout · card orders +3% · Sales terms & conditions — please review before ordering. For Research Use Only. Not for diagnostic or therapeutic use.
Questions? Talk to us 1-866-986-9598 orders@biohippo.com

Overview

What is BeaverBeads Mag COOH Carboxyl Magnetic Polymer Beads, 300 nm?

Product Overview

BeaverBeads™ Mag COOH-300 are monodisperse superparamagnetic microspheres with an Fe3O4 core and a hydrophilic polymer shell carrying surface carboxyl groups. At 300 nm they sit at the small end of the BeaverBeads COOH range, where the very high surface-area-to-volume ratio maximises capture efficiency per milligram of bead and the particles stay suspended long enough for homogeneous binding kinetics.

Surface carboxyls are activated with EDC and NHS and coupled through stable amide bonds to any ligand bearing a primary amine — antibodies, proteins, peptides and amine-modified oligonucleotides. The result is a custom capture reagent with the low non-specific binding and tight size distribution that quantitative immunoassays require.

How it works

Beads are washed into MES buffer at pH 5.0, activated with freshly prepared EDC and NHS for 30 minutes at 25 °C, then coupled to 50–200 µg of ligand at pH 8.0. After coupling, residual activated sites are blocked and the conjugate is washed into a storage buffer. The manufacturer's manuals under Documents give the full procedure and quenching conditions.

Applications

Magnetic chemiluminescent immunoassay (CLIA) development, immunoprecipitation, cell sorting, phage display screening, targeted nucleic acid capture, biosensor construction, and drug screening and delivery studies.

Choosing the right size

The Mag COOH series is supplied at 300 nm (this product, Cat. 70106), 500 nm, 1 µm, 2 µm and 5 µm. Carboxyl density rises with particle size in this family — roughly 60 µmol/g at 300 nm against 200–250 µmol/g at 1–5 µm — but the smaller bead gives faster, more homogeneous binding and stays dispersed longer. Choose 300 nm when binding kinetics and suspension stability matter more than absolute capacity per gram; choose the larger sizes when you need faster magnetic pelleting or higher capacity. Where an agarose matrix and much lower background are preferred, see BeaverBeads Magrose COOH.

Handling and safety

Do not freeze, dry out or centrifuge these beads — each causes irreversible aggregation and loss of surface activity. Vortex or sonicate briefly before every use; sub-micron beads settle during storage. A magnetic separator is required, and separation of 300 nm particles takes longer than for micron beads. Keep beads and separators away from metal objects, electronic devices and implanted electronic devices such as cardiac pacemakers.

For Research Use Only. Not for use in diagnostic or therapeutic procedures. Specifications are those published by the manufacturer, BEAVER Biomedical Engineering Co., Ltd.

Details

Specifications

ApplicationsImmunoprecipitation, Protein Purification, Bioconjugation, Chemiluminescence Immunoassay, Cell Separation
Concentration10 mg/mL
FormAqueous magnetic bead suspension
StorageStore at 2-8 C. Do not freeze, dry or centrifuge - all cause irreversible aggregation and loss of surface activity.
Storage bufferSupplied in purified water; the manufacturer recommends transferring to 20% (v/v) ethanol for long-term storage.
ShippingAmbient temperature
Unit of measuremL
Catalog no. (Mfr.)70106, 70106-5, 70106-50
Main SKUBHD13200044

Applications

Applications & how to use

Immunoprecipitation (IP)

Enriches a target protein and its interacting partners from lysate using an antibody coupled to beads. Used for interaction studies and downstream WB or MS.

Protein Purification

Separating a target protein from a complex mixture while keeping it folded and active, using chromatography, spin columns, selective binding or buffer exchange. Recovery and retained activity matter more than purity alone, so an activity assay should accompany the gel at each step.

Bioconjugation

Covalent attachment of a biological ligand — antibody, protein, peptide or oligonucleotide — to a surface or another molecule. The chemistry chosen determines orientation and retained activity, so coupling through a residue distant from the binding site usually matters more than raw coupling efficiency.

Chemiluminescence Immunoassay (CLIA)

Immunoassay read by light emitted from an enzymatic or direct chemiluminescent label, giving wider dynamic range and lower detection limits than colorimetric ELISA. Magnetic microspheres are the usual solid phase, so bead uniformity and low non-specific binding translate directly into assay sensitivity and reproducibility.

Cell Separation

Isolation of a defined cell population from a mixed suspension, most often by antibody-coated magnetic beads in positive or negative selection format. Negative selection leaves the target untouched by antibody, which is preferred when downstream function or receptor availability could be affected by bead binding.

Evidence

Validation & QC

Validation data for this product isn’t published yet.

Need specific QC or validation results — titer, purity, endotoxin, or assay data — for your application? Our scientific team can share what is available for this product and lot on request.

Request validation data

Manufacturing

How it's made & quality control

Supplier quality control

Magnetic and functionalized beads are QC-tested for size uniformity, binding capacity and lot-to-lot consistency for reproducible separation and purification.

Product sheets provide bead size, surface chemistry, binding capacity and recommended protocols.

Certificate of Analysis provided per lot with binding-capacity data.

Supplier-level quality statement. For lot-specific results, request the Certificate of Analysis for your batch.

Questions

Frequently asked questions

Which BeaverBeads COOH size should I choose?

The series covers 300 nm (this product), 500 nm, 1 um, 2 um and 5 um. Carboxyl density rises with size - about 60 umol/g at 300 nm against 200-250 umol/g at 1-5 um - but smaller beads bind faster and stay suspended longer. Pick 300 nm for kinetics and suspension stability, larger sizes for capacity and faster pelleting.

How long does magnetic separation take at 300 nm?

Longer than for micron beads. Sub-micron superparamagnetic particles respond more slowly to the same field, so allow extra time on the separator and confirm the supernatant is clear before discarding it. A stronger separator shortens the step.

What coupling chemistry do these beads use?

Standard EDC/NHS carbodiimide chemistry. Surface carboxyls are activated at pH 5.0 in MES buffer, then coupled to primary amines at pH 8.0. No proprietary reagent is required.

Are they compatible with automated platforms?

Yes, with the caveat above about slower magnetic response. They work on magnetic-rod and plate-based workstations; validate the separation dwell time on your specific instrument before running samples.

Why do the beads clump, and can I recover them?

Clumping follows freezing, drying, centrifugation, or prolonged time in a strong magnetic field. Field-induced clumping usually disperses with 2 minutes in an ultrasonic bath. Aggregation from freezing, drying or centrifugation is irreversible.

Answered by our team

Questions from researchers

No researcher questions have been answered for this product yet. Ask our technical team and we'll get back to you — approved answers are published here.

Ask our technical team

Reviewed by a scientist — typically answered within one business day.

Deals

Promotions

Codes apply at checkout

Customization

Customization & add-ons

BEAVER manufactures magnetic beads at scale and supports OEM and ODM supply. The following are available through BioHippo - contact support@biohippo.com for scope and pricing.

  • Bulk volumes: beyond the catalogue pack sizes, including litre-scale production.
  • Custom functionalisation: alternative surface groups (NH2, NHS, OH, streptavidin) and custom carboxyl densities.
  • Pre-coupled beads: your antibody or protein covalently immobilised by the manufacturer.
  • Custom particle sizes: outside the standard 300 nm to 5 um range.
  • OEM / ODM supply: for chemiluminescent immunoassay and diagnostic kit manufacturers.
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