BeaverBeads GSH Magnetic Beads for GST Fusion Protein Purification - Figure 1 of 2

BeaverBeads GSH magnetic beads as supplied by BEAVER Biomedical Engineering.

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Beaver Biomedical Engineering Co Ltd
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Beaver Biomedical Engineering Co Ltd

BeaverBeads GSH Magnetic Beads for GST Fusion Protein Purification

SKU BHD13200060 · Cat# 70601, 70601-5, 70601-K10, 70601-100, 70601-1000
In Stock at ManufacturerNew

BeaverBeads GSH are glutathione-functionalised superparamagnetic agarose beads (30-150 um) that bind up to 10 mg of GST fusion protein per mL of beads. They purify GST-tagged proteins from crude lysate in a single magnetic step, with mild elution in reduced glutathione that preserves biological activity.

At a glance
Ligand
Glutathione (GSH)
Target
GST-tagged fusion proteins
Binding Capacity
Up to 10 mg/mL beads
Bead Diameter
30-150 um
Matrix
Magnetic agarose (Fe3O4 core)
Suspension
10% (v/v)
Elution
10 mM reduced glutathione, pH 8.0 (native)
Storage
4-8 C in 20% ethanol
See all 5 configurations
All configurations · 5 options
Catalog No.SizeAvailability Price Qty Order
70601-55 mLIn Stock at Manufacturer $580.00
Quote
70601-K10Kit, 5 mL (10 reactions)In Stock at Manufacturer $580.00
Quote
70601-1002 x 50 mLIn Stock at Manufacturer $5,000.00
Quote
70601-10004 x 250 mLMade to Order Quote—
70601Other size - enquireMade to Order Quote—
Ambient temperature Store at 4-30 C; 4-8 C recommended for long-term storage. Do not freeze, dry or centrifuge. 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 GSH Magnetic Beads for GST Fusion Protein Purification?

Product Overview

BeaverBeads™ GSH are superparamagnetic agarose microspheres presenting immobilised glutathione, the natural ligand of glutathione S-transferase. They capture GST-tagged recombinant proteins directly from crude lysate and release them under mild, non-denaturing conditions with free reduced glutathione — a single-step purification that preserves the biological activity of the target.

Because separation is magnetic, the workflow avoids the steps that make column chromatography slow: no high-speed clarification of the crude sample, no filtration, no flow-rate control and no chromatography hardware. The manufacturer reports that a skilled operator can obtain highly purified protein in under one hour, and that parallel processing of many samples scales without additional equipment.

Binding capacity and performance

Up to 10 mg of GST fusion protein bound per mL of beads. Capacity is quoted against 100% beads; the product is supplied as a 10% (v/v) suspension, so 1 mL of suspension contains 100 µL of beads. Actual capacity depends on the size, folding and accessibility of the GST fusion partner, so the manufacturer states this as a reference value rather than a guarantee.

Purification workflow

Binding and washing use Buffer A (140 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, 1.8 mM KH2PO4, pH 7.4). Elution uses Buffer B (50 mM Tris-HCl with 10 mM reduced glutathione, pH 8.0), prepared fresh because reduced glutathione oxidises readily. Tightly bound fusions can be recovered by extending the elution time, repeating the elution, or raising the glutathione concentration.

Beads are then regenerated: alternating high-pH (0.1 M Tris-HCl, 0.5 M NaCl, pH 8.5) and low-pH (0.1 M sodium acetate, 0.5 M NaCl, pH 4.5) washes for light use; 6 M guanidine hydrochloride followed by PBS to strip denatured or precipitated protein; 70% ethanol or 0.1% non-ionic detergent to remove hydrophobic contaminants.

Applications

Purification of GST-tagged recombinant proteins from bacterial, insect and mammalian expression systems; GST pull-down assays for protein–protein interaction mapping; immunoprecipitation using GST-fusion bait; and purification of glutathione transferases and other glutathione-binding proteins. Suitable for both research-scale and process-development work, manually or on automated magnetic workstations.

Handling and safety

Do not freeze, dry out or centrifuge the beads — each causes irreversible aggregation. Resuspend fully before every use. A magnetic separator is required. Prepare the glutathione elution buffer immediately before use. 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

TargetGlutathione S-transferase (GST) fusion proteins
ApplicationsProtein Purification, Immunoprecipitation, Protein Interaction
TagGST
Concentration10% (v/v) bead suspension (1 mL suspension = 100 uL beads)
FormAqueous magnetic bead suspension
StorageStore at 4-30 C; 4-8 C recommended for long-term storage. Do not freeze, dry or centrifuge.
Storage buffer20% (v/v) ethanol
ShippingAmbient temperature
Unit of measuremL
Catalog no. (Mfr.)70601, 70601-5, 70601-K10, 70601-100, 70601-1000
Main SKUBHD13200060

Applications

Applications & how to use

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.

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 Interaction

Detects and quantifies binding between a protein and a partner molecule, whether another protein, a nucleic acid, a lipid or a small molecule. Readouts range from gel shift and pull-down to fluorescence and label-free biophysics, and are used to confirm complex formation and measure affinity.

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.

Resources

Documents & downloads

Questions

Frequently asked questions

How much GST fusion protein will these beads bind?

Up to 10 mg per mL of beads. Note the product is a 10% (v/v) suspension, so 1 mL of what you pipette contains 100 uL of beads. Real capacity depends on the size and folding of your fusion partner, so treat 10 mg/mL as a ceiling and titrate.

How do I elute without denaturing my protein?

Compete the GST-glutathione interaction with free reduced glutathione: 50 mM Tris-HCl, 10 mM reduced glutathione, pH 8.0. This is a native elution - the protein keeps its activity. Make the buffer fresh, because reduced glutathione oxidises quickly and an oxidised buffer elutes poorly.

My protein will not come off. What now?

Extend the elution incubation, elute a second and third time, or raise the glutathione concentration above 10 mM. Some fusions bind tightly enough to need all three. If it still will not elute, check that the GST tag is not sterically buried by the partner protein.

Can I reuse the beads?

Yes. For light use, alternate high-pH (0.1 M Tris-HCl, 0.5 M NaCl, pH 8.5) and low-pH (0.1 M sodium acetate, 0.5 M NaCl, pH 4.5) washes three times. If capacity has dropped because denatured protein has accumulated, strip with 6 M guanidine hydrochloride then wash three times in PBS. For hydrophobic contaminants, wash with 70% ethanol or 0.1% non-ionic detergent.

Do I need to clarify my lysate first?

Not to the degree column chromatography demands. That is the point of magnetic separation - no high-speed clarification, no filtration, no flow-rate control. Remove gross debris and proceed.

What is the difference between 70601 and 70601-K10?

70601-5 supplies beads only. 70601-K10 is BEAVER's kit format at the same 5 mL volume, configured for 10 purification reactions. The full buffer component list for the kit is not published in the current datasheet - contact us to confirm before ordering.

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.

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Customization

Customization & add-ons

BEAVER manufactures affinity 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 4 x 250 mL catalogue pack, including litre-scale production.
  • Related affinity chemistries: IDA-Nickel and IDA-Cobalt for His-tag, Strep-Tactin for Strep-tag II, Protein A / G / A-G for antibodies, Heparin and DEAE for ion exchange.
  • Custom ligand immobilisation: your ligand coupled to the Magrose matrix by the manufacturer.
  • OEM / ODM supply: for kit and instrument manufacturers.
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