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Sepax Antibodix Columns
Sepax Antibodix Columns
Origin of place United States
Model
Supplier Sepax Technologies, Inc.
Price
Hits 854
Updated 4/1/2013
  • Product Detail
  • Company Profile

Description

Antibodix columns are specially designed for high resolution, high efficiency and high recovery separations of antibodies. The packing support is composed of a rigid, spherical, highly cross-linked poly(styrene divinylbenzene) (PS/DVB) non-porous bead. The non-porous resin has particle size of 1.7, 3, 5 and 10 µm. The PS/DVB resin surface is grafted with a highly hydrophilic, neutral polymer thin layer with the thickness in the range of nanometer. On the top of the hydrophilic layer, weak cation-exchange functional groups are attached via a proprietary chemistry, resulting in high capacity ion-exchange layer.
Packing

 


Support: High cross-linked, spherical PS/DVB beads
Particle size: 1.7, 3, 5 and 10 µm
Pore size: non-porous
Phase structure: weak cation exchanger with carboxylate functional groups chemically bonded and hydrophilic


Characteristic

  • Highly cross-linked non-porous PS/DVB particle as the support
  • Uniform particle size
  • Particle size availability: 1.7, 3, 5, and 10 µm
  • Weak-cation exchange chemistry
  • Hydrophilic surface specially designed for elimination of non-specific bindings
  • High separation efficiency, selectivity and resolving power
  • High lot-to-lot reproducibility (link to below header)
  • High loading capacity (link to below header)
  • High recovery
  • High mechanical stability with pressure tolerance higher than 8,000 psi for 5 and 10 µm, and 10,000 psi for 1.7 and 3 µm
  • High pH stability: 2-12
  • Well suited for UPLC and regular HPLC systems
  • Complete selection for analytical, semi-preparative and preparative separations
  • Applications for proteins, especially antibodies

Chromatogram of a protein mixture separated by Antibodix NP5, 7.8×50mm

Conditions  
Column: Antibodix NP5 (5 µm, 7.8×50 mm)
Mobile phase: A: 10 mM phosphate buffer, pH 6
B: A + 1.0 M NaCl
Gradient: 10-45%B (21 min)
Flow rate: 1.5 mL/min
Temperature: Ambient
Injection volume: 10 µL
Sample: 1. Cytochrome C
2. Lysozyme
3. Ribonuclease A

Separation of MAb on Antibodix NP1.7 (1.7 µm, 4.6×50 mm) 
 

Conditions  
Column: Antibodix NP1.7 (1.7 µm, 4.6×50 mm)
Mobile phase: A. 10 mM phosphate buffer, pH 7.5
B. A + 100 mM NaCl
Gradient: 15-55% B (30 min)
Flow rate: 0.3 mL/min
Detector: UV 214 nm
Temperature: Ambient
Injection volume: 5 µL
Sample: Monoclonal antibody (5 mg/mL)

High lot to lot reproducibility

Sample 1. Protein mixtures 

Conditions  
Column: Antibodix NP10 (10 µm, 4.6×250 mm)
Mobile phase: A: 10 mM phosphate buffer, pH 7.5
B: A + 100 mM NaCl
Gradient: 15-55%B (30 min)
Flow rate: 0.8 mL/min
Temperature: Ambient
Detector: UV 214 nm
Injection volume: 5 µL
Sample: 1. Cytochrome C (5 mg/mL)
2. Lysozyme (5 mg/mL)
3. Ribonuclease A (5 mg/mL)

Sample 2. Monoclonal antibodies 
 

Conditions  
Column: Antibodix NP10 (10 µm, 4.6×250 mm)
Mobile phase: A. 10 mM phosphate buffer, pH 7.5
B. A + 100 mM NaCl
Gradient: 15-55% B (30 min)
Flow rate: 0.8 mL/min
Temperature: Ambient
Detector: UV 214 nm
Injection volume: 5 µL
Sample: Monoclonal antibody (5 mg/mL)

High Loading

Conditions  
Column: Antibodix NP10 (10 µm, 4.6×250 mm)
Mobile phase: A: 10 mM phosphate buffer, pH 6
B: A + 1.0 M NaCl
Gradient: 10-100%B (25 min)
Flow rate: 0.8 mL/min
Temperature: Ambient
Detector: UV 214 nm
Sample: 1. Aprotinin (3.3 mg/mL)
2. Lysozyme (5.6 mg/mL)
3. Ribonuclease (3.0 mg/mL)

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