Affinity Media

Protein G SepFast Media

£156.79£10,482.23 ex. VAT

Description

Protein G SepFast Media is a family of affinity resins with protein G immobilised to highly cross-linked agarose-based beads of various sizes.

  • Protein G SepFast HighRes: 20 – 50 µm, good for small column run at shorter residence time (i.e. higher flowrate)
  • Protein G SepFast: 50 – 150 µm, good for most applications from small scale to large scale purification requirements (i.e. low column pressure);
  • Protein G SepFast Large Bead: 150 – 350 µm, particularly good for processing viscous or cell-containing feedstocks (i.e. high settling rate and extremely low column pressure)

Protein G binds to the Fc region of IgG from a variety of mammalian species. Protein G SepFast may be used to isolate and purify classes, subclasses and fragments of Immunoglobulins from any biological fluid or cell culture medium. Protein G SepFast is extremely useful for isolation of immune complexes.

The potential applications of protein G include practically all of the current and projected applications of protein A. Protein G and protein A, however, have different IgG binding specificities, dependent on the origin of the IgG. Compared to protein A, protein G binds more strongly to polyclonal IgG, for example, from cow, sheep and horse. Furthermore, unlike protein A, protein G binds polyclonal rat IgG, human IgG3 and mouse IgG1.

Protein G SepFast is developed and supported for production scale chromatography. BioToolomics offers both loose medium and pre-packed ready-to-use disposable columns.

Further information about Protein G SepFast.

Characteristics of Protein G SepFast Media

Matrix

Highly cross-linked agarose bead

Particle Size

20 – 50 µm Protein G SepFast HighRes
50 – 150 µm Protein G SepFast
150 – 350 µm Protein G SepFast Large Bead

Max. Operating Pressure

0.3 MPa (3 bar, 42 psi)

Binding Capacity**

≥ 15 mg human IgG/mL resin

**Please note that there might be considerable deviations in binding capacity for different immunoglobulins derived from the same species, even if they are of the same subclass.

Chemical Compatibility

The commonly used reagents for antibody purifications

Chemical Stability

Stable in most commonly used buffers, 6 M guanidine-HCl; 70% ethanol, 8 M urea, pH 10.5; 0.1 M Glycine-NaOH, pH 11

Physical Stability

Negligible volume variation due to changes in pH or ionic strength

pH Stability

3 to 9 (long term); 2 to 10 (short term)

Sanitisation

Sanitise the column with 70% ethanol

Storage & Temperature

20% ethanol at 2°C – 8°C