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Resin parameters

Matrix
Agarose 4%
Particle Sizes
45–165
Recommended Flow Rate
90~200 cm/h
Maximum Flow Rate
250 cm/h
Maximum Working Pressure
3 bar
maximum temperature
4–30°C
Separation Range, kDA
60–20,000 (spherical molecules) | 20–6,000 (linear molecules)
Swelling Coefficient
ND
* When the column bed height is ≥ 60 cm, it is recommended that the flow rate is reduced to 45~60 cm/h.

Chemical resistance

pH Stability
2–14
Chemical Stability
All commonly used aqueous buffers, 30% isopropanol**, 75% ethanol**, 1M NaOH, 1M acetic acid, 6M guanidine hydrochloride, 8M urea
The physical and chemical properties and functions of the chromatographic resin have no obvious changes after being placed in an environment of 40°C and pH 2–14 for 7 days.

Resin description

Persefose 4FF is a highly cross-linked agarose-based gel filtration SEC resin (cross-linking ratio 4%), which separates different molecules by using their molecular weight and conformation differences. It can be used successfully for the separation and purification of a wide range of biological molecules such as recombinant proteins, antibodies, nucleic acids, viruses and virus-like particles, and polysaccharides.

Persefose 4FF has excellent scale-up capabilities:

  • A highly cross-linked agarose matrix with excellent rigidity. This reduces the restriction on column bed height and allows a high process flow rate under low back pressure, improving process efficiency.
  • An improved bead-making process achieves a smaller diffusion effect and provides better resolution.

Method of use

Chromatographic conditions

Buffer selection. Consider the stability of the sample in the buffer. To avoid possible non-specific adsorption, use a salt-containing buffer rather than ultrapure or pure water.

Flow rate. Generally use a linear flow rate of 90~200 cm/h, according to the height of the column bed. Where the column bed height is ≥ 60 cm, reduce the flow rate to 45~60 cm/h.

Sample pretreatment. Filter the sample through a 0.45 µm microporous membrane before loading to prevent the sample from clogging the column.

Chromatography steps

  1. Equilibration. Use the buffer to fully equilibrate the chromatography column until the pH and conductivity are stable and basically consistent with the equilibration buffer. This step usually requires 1–2 column bed volumes (CV).
  2. Sample loading. The usual loading volume is 1%–5% of the column volume. The sample concentration should not be too high, to avoid overpressure or affecting the resolution.
  3. Elution. Use buffer to elute, collecting the components that elute at different positions, usually over 1~1.5 CV.
  4. Regeneration. Rinse the column with a high-salt buffer (such as 1M NaCl).
  5. Re-equilibration. Re-equilibrate the column with buffer.

Cleaning and regeneration

Contaminants (e.g. lipids, endotoxins and proteins) accumulate on the column as the number of uses of the chromatography resin increases. Regular cleaning-in-place (CIP) is essential to keep the column in a stable working condition. Determine the frequency of CIP according to the degree of contamination of the chromatography resin. Where contamination is considerable, CIP after each use is recommended to ensure repeatability of results and to prolong the working life of the chromatography resin.

For different types of impurities and contaminants, the recommended cleaning conditions are as follows:

  • Strongly binding proteins: wash with 5 CV of 2M NaCl solution, or use a high-salt buffer with a pH not lower than 2, such as 1M NaAc solution.
  • Strongly hydrophobic proteins and precipitated proteins: first wash with 5 CV of 1M NaOH solution, then wash out the lye with 5–10 CV of ultrapure or pure water.
  • Lipoproteins and lipids: first wash with 5 CV of 70% ethanol or 30% isopropanol, then rinse with 5–10 CV of ultrapure or pure water.

Degas 70% ethanol or 30% isopropanol before use. The flow rate should be 30–60 cm/h during CIP. Use reverse cleaning where the clogging is severe. To reduce the microbial load, treat the chromatography resin with 0.5–1M NaOH solution for 15–30 minutes.

Storage

Keep the unopened chromatography resin in the original container and store at 4~30°C in a well-ventilated, dry and clean place. Do not freeze. Wash the used column with 2–3 CV of 20% ethanol solution and store at 2~8°C.

Destruction and recycling

Since chromatography resin is difficult to degrade in nature, it is recommended that the waste chromatography resin is incinerated to protect the environment. For chromatography resin that has been in contact with biologically active samples such as viruses and blood, follow the local biosafety requirements before destroying or disposing of it.

Packing method

Detailed information on resin packaging is available on request. Please contact your local distributor.

Ordering information

  • 701-00025 — 25 ml
  • 701-00100 — 100 ml
  • 701-00500 — 500 ml
  • 701-01000 — 1 L
  • 701-05000 — 5 L
  • 701-10000 — 10 L
  • 701-20000 — 20 L
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