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Stock Code 300487
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Agarose-Based Chromatography Resins
Agarose-Based Chromatography Resins
Size Exclusion Chromatography – Agarose
Size Exclusion Chromatography – Agarose

Seplife® 4AG/90

  • Industrial-scale fractionation of large biomolecules and virus particles
  • Hydrophilic base matrix ensures very low levels of non-specific adsorption and high recovery rate
  • Designed to fractionate proteins of 4×104–3×10⁷ Da
  • Seplife® 4AG/90 is a size exclusion chromatography resin designed for industrial processing at high flow rate.
    Seplife® 4AG/90 is size exclusion chromatographic resin based on 4% cross-linked agarose with a large particle size (45-165 micron).
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Products

Properties

Product

Seplife® 4AG/90

Appearance

White spherical beads

Type

Size exclusion agarose

Matrix

4% crossed linked agarose

Particle size range (μm)

45-165

Selectivity: Kav IgG 150000MW

0.66-0.76

pH stability

3-13 (operational), 2-14 (CIP)

Chemical Stability

Stable in all common aqueous buffers; 1M sodium hydroxide; 8M urea; 6M guanidine hydrochloride; 70% ethanol.

Flow rate* (cm/h)

max 420cm/h

Shipped as

20% ethanol slurry

*Testing conditions: Chromatography column 16mm×400mm; column bed height 25cm; temperature 25°C; mobile phase water.

Instructions

Column packing

Column loading should be performed in accordance with standard operating procedures. It is important to ensure that each material is at its working temperature, and the media may need to be degassed before column packing.

Equilibration

Equilibrate the column with an appropriate 2-5 column volume buffer. Ensure the conductivity and pH of the effluent are the same as the equilibration buffer.

Sample feeding

1. Samples are prepared in buffer, and cloudy samples need to be centrifuged and filtered before loading. Samples with too high salt content and too low concentration should be processed first before loading.

2.The separation of components in the sample by the media is carried out according to the molecular size of the components. The ones with the larger molecular size flow out first.

3. The sample loading volume is about 1-2% of the column volume. The smaller the loading volume, the better the separation.

Elution

Elute with buffer, keep the flow rate and buffer composition unchanged during elution.

Regeneration

Generally, wash with buffer solution to balance and the media can be used again. Inactivated proteins or lipids that cannot be washed out during regeneration, can be removed by Cleaning-In-Place (CIP).

Cleaning-In-Place (CIP)

1. For proteins bound by ionic bonds, 0.5~1 BV of 2M NaCl can be used to remove them.

2. For precipitated proteins, hydrophobically bound proteins or lipids, wash with 1 BV of 0.1M NaOH.

3. For proteins and lipids with strong hydrophobic binding, wash with 4-10 BV of 70% ethanol or 30% isopropanol.

4. The concentration of the organic solvent should gradually increase to avoid bubbles.

After cleaning, equilibrate the column with equilibration buffer solution at least 3 times the volume of the column bed until the pH and conductivity remain unchanged.

Storage

Sealed and stored at 4~30°C (preservation solution is 20% ethanol), in a ventilated, dry and clean place, do not freeze. 

Ordering information

Product Name

References

Pack Size

Seplife®4AG/90

A1003102

25ml

A1003103

100ml

A1003104

500ml

A1003105

1L

A1003106

5L

A1003107

10L

Production date: See label

Expiry Date: 5 years, under proper storage conditions

 

Manufacturer: Sunresin New Materials Co. Ltd.

Add:No. 135, Jinye Rd, Xi'an Hi-tech Industrial Development Zone, Shaanxi, 710076, China

www.seplite.com    www.sunresin.com

E-mail: info.lifescience@sunresin.com

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