Welcome to our new website!

【New Product Release】Novel Macroporous Polymer-Based Ion Exchange Medium

Novel Macroporous Polymer-Based Ion Exchange Medi

Ion exchange chromatography is the most commonly used method for the separation and purification of biomacromolecules. The target protein interacts electrostatically with the ion exchange resin, and separation is achieved through the exchange of proteins with ions of the same charge on the surface of the resin. Depending on the type and strength of charges on the protein surface, cation exchange or anion exchange resins can be chosen as needed for the separation process.


Welch's Polymate IEC series ion exchange resins are based on polymers, offering excellent physical and chemical stability as well as higher mechanical strength. Through surface hydrophilic treatment, they exhibit excellent compatibility with biologically active macromolecules, allowing for the modification of different ion groups.


This series of products features large pores, high flow rates, and low back pressure, making them widely applicable for the separation and purification of antibodies, proteins, insulin, peptides, nucleic acids, antibiotics, natural products, and more. The large pore size is particularly suitable for the separation of large molecular proteins such as vaccine antigens, viruses, recombinant proteins, and antibodies.




 Polymate IEC Ion Exchange Chromatography Medium  


The Polymate IEC chromatography medium introduced by Welch Materials utilizes hydrophilically modified acrylic ester polymers as the backbone, with a pore size of up to 2500Å. Its pressure resistance and mass transfer properties are both outstanding.


Product Features


01Technical Specifications

Types of Packing SP CM Q DEAE
Matrix
Polymethacrylate
Activation Groups Sulfopropyl carboxymethyl  Quaternary Ammonium

Diethyl Aminoethyl

Shape
Spherical
Average Particle Size
60μm, distribution 48-88μm
Pore Size
~2500Å
Ion Content

0.15meq

/mL

0.4meq

/mL

0.15meq

/mL

0.15meq

/mL

Dynamic Capacity 25mg/mL 35mg/mL 25mg/mL 20mg/mL
Max. Pressure
2MPa
Storage
20% ethanol

02 Flow Rate-Pressure Relationship



The flow rate-pressure relationship of Polymate IEC ion exchange chromatography medium


03 Application of Packing


(1) Column Packing

  1. Calculate the column volume to be packed, and use 1.3 times the volume of the column for the packing material.
  2. Prepare a suspension of the packing material with approximately 50% concentration using a 0.2M sodium chloride solution.

  3. Pour the suspended packing material into the chromatography column and pack it using a constant pressure of 0.2 MPa.

  4. Once the packing height stabilizes, mark the position and scale, then lower the column head to 3mm below the marked scale line. Tighten the column head seal ring to complete the column packing.


(2) Instructions for Use

The typical usage of a new chromatography column involves several steps including equilibration, sample loading, washing, elution, and regeneration.

  1. Equilibration: Prior to use, equilibrate the newly packed chromatography column with at least 10 column volumes (CV) of equilibration buffer (e.g., 20mM or 50mM PBS or Tris HCl pH 7.2) until all baselines stabilize.

  2. Sample Loading: Prepare the sample preferably in equilibration buffer and filter it using a 0.45μm filter membrane. Load the sample according to 80% of the dynamic capacity.

  3. Washing: After sample loading, continue washing the column with equilibration buffer until the baselines stabilize.

  4. Elution: Perform elution by washing the column with elution buffer (e.g., high salt buffer containing 1.5M sodium chloride) until the baselines stabilize, and collect the eluate.

  5. Regeneration: After each chromatography run, wash the column with 1-2M NaCl solution to remove proteins strongly bound to the medium.

  6. In-situ Cleaning: If significant decrease in medium capacity occurs, further clean the column with 5-10 column volumes of 0.1M-0.5M sodium hydroxide to remove strongly bound proteins. Then rinse the column with equilibration buffer until neutral.

  7. Storage: After usage, flush the column with a large volume of ultrapure water to replace the buffer inside the column, followed by 20% ethanol, and seal it for storage in a refrigerator (2-5°C).

(3) Storage of Packing Material

Ion exchange chromatography packing material is initially stored in 20% ethanol upon leaving the factory and should be stored tightly sealed at 2-5°C in a refrigerator. It is recommended to replace the storage solution every two months.



Order Information  (25/100/500mL,1/5L)

Pre-packed Column Order Information  

(1/5 mL)

 Polymate EP Polymer-based Epoxy-Activated  Medium

The matrix (Polymate EP) surface contains a large number of epoxy groups, with a pore size of 2500Å. It features convenience in use, mild coupling conditions, high coupling efficiency, and a wide range of applications, making it suitable for direct coupling with various ligands.


Welch Polymate series microsphere microscopy image


Product Characteristics


01 Technical Parameters


Parameters Polymate EP
Matrix Acrylic Ester
Ligand Bonding Method Epoxy Bonding
Particle Size Epoxy Bonding
Pore Size 2500Å
Activation Group Density >40μmol/mL wet gel
Maximum Pressure Resistance 2MPa
pH Stability 2-13
Storage Conditions 2~8℃, 20% ethanol

02 Flow Rate-Pressure Relationship


Flow rate-pressure relationship graph for Polymate EP chromatography medium.


Note: All products listed in the order form are available for sample trials and can also be customized to other specifications according to customer requirements.




We will soon introduce more high-performance products. Stay tuned for updates!