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AB270237

Glutathione Affinity Resin - Amintra

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(3 Publications)

Glutathione Affinity Resin - Amintra® (ab270237) is designed for simple, rapid purification of Glutathione-S-transferase (GST)-tagged recombinant proteins produced using the pGEX series of expression vectors, other glutathione -S-transferases and glutathione binding proteins from bacteria, yeast, insect and mammalian cultures.

Key facts

Form

Liquid

form

Storage buffer

pH: 6 - 8 Constituents: Agarose beads, 20% Ethanol

storage-buffer

Product details

Glutathione Affinity Resin - Amintra® (ab270237) is designed for simple, rapid purification of Glutathione-S-transferase (GST)-tagged recombinant proteins produced using the pGEX series of expression vectors, other glutathione -S-transferases and glutathione binding proteins from bacteria, yeast, insect and mammalian cultures. GST-tagged proteins can be purified directly from pre-treated bacterial lysates using Glutathione Affinity Resin - Amintra®. The tagged proteins are eluted under mild, nondenaturing conditions that preserve protein antigenicity and function.

This product is manufactured by Expedeon, an Abcam company, and was previously called Amintra® Glutathione Affinity Resin. Expedeon product codes AGS0010 (10 mL Medium), AGS0025 (25 mL Medium) and AGS0100 (100 mL Medium) are the same as the current sizes: 10 mL, 25 mL, and 100 mL, respectively.

The glutathione ligand is coupled to highly cross-linked 4% agarose beads. The coupling is optimized to give high binding capacity for GST-tagged proteins and other glutathione binding proteins. Glutathione Affinity Resin - Amintra® can purify GST-tagged proteins under high flow rate. Its high flow properties make it excellent for scale-up.

Glutathione Affinity Resin - Amintra® is stable with all commonly used buffers and reagents including 0.1M NaOH and organic solvents. Removal of the GST tag can be performed whilst the fusion protein is bound to the column or in solution after elution.

Characterization of the Resin

  • Supporting matrix: 4% highly crosslinked agarose resin
  • Bead size range: 45-165 μm
  • Recommended working pH: pH 3.0-12.0
  • Typical binding capacity: > 10mg GST-tagged protein/ml resin
  • Recommended Flow rate*: 100 – 300 cm/h
  • Maximum Flow rate: 450 cm/h
  • Maximum pressure: 3 bar, 43 psi
  • Chemical stability: High
  • Solubility in water: Insoluble
  • Ligand: The glutathione ligand is coupled via a 12-atom linker
  • Ligand concentration: 120-320 μmol glutathione/ml medium

* Binding of GST to glutathione is flow dependent and lower flow rates often increase the binding capacity. This is important during sample loading and elution. Protein characteristics, pH and temperature may also affect the binding
capacity.

Properties and storage information

Shipped at conditions
Ambient - Cannot Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Do Not Freeze

Product protocols

Target data

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

Scientific reports 9:13820 PubMed31554828

2019

Bioorthogonal protein-DNA conjugation methods for force spectroscopy.

Applications

Unspecified application

Species

Unspecified reactive species

Marie Synakewicz,Daniela Bauer,Matthias Rief,Laura S Itzhaki

Cancer cell 35:519-533.e8 PubMed30889383

2019

DNA Replication Vulnerabilities Render Ovarian Cancer Cells Sensitive to Poly(ADP-Ribose) Glycohydrolase Inhibitors.

Applications

Unspecified application

Species

Unspecified reactive species

Nisha Pillay,Anthony Tighe,Louisa Nelson,Samantha Littler,Camilla Coulson-Gilmer,Nourdine Bah,Anya Golder,Bjorn Bakker,Diana C J Spierings,Dominic I James,Kate M Smith,Allan M Jordan,Robert D Morgan,Donald J Ogilvie,Floris Foijer,Dean A Jackson,Stephen S Taylor

Cell chemical biology 25:1117-1127.e4 PubMed30017913

2018

The MALDI-TOF E2/E3 Ligase Assay as Universal Tool for Drug Discovery in the Ubiquitin Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Virginia De Cesare,Clare Johnson,Victoria Barlow,James Hastie,Axel Knebel,Matthias Trost
View all publications
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