Magnetic Microspheres
Latex Microspheres
Dyed Microspheres
Fluorescent Microspheres
Flow Cytometry Microspheres
Standard Microspheres
Size Exclusion Resins
Focurose 30PG
Focurose 200PG
Focurose 75PG
Focurose 6FF
Focurose 4FF
Ion Exchange Resins
Affinity Resins
Hydrophobic Interaction Resins
Multimodal Resins
Pre-activated Resins
Homogeneous Luminescent Immunoassay
Instruments and Reagent
Focurose 4FF
sample

Focurose 4FF is suitable for component separation and moderate purification of biomacromolecules (removal of small molecule impurities), such as viral particles, large molecular proteins, recombinant hepatitis B surface antigen, polysaccharides, and macromolecular complexes.

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Features

  • High (physicochemical) stability, high flow rate (component separation), and high recovery rate (up to 95%)

  • Mild elution conditions that preserve the biological activity and functionality of biomacromolecules

  • Easy to scale up

  • Easy to maintain


Focurose 4FF Performance Parameters    

 

Resin

Highly cross-linked 4% agarose

Particle size range  

45-165µm

Average particle size (D50)

90±5µm

Separation range (globular proteins)

60-20000 kDa

pH stability

2-12 (long-term) 2-14 (short-term)

Chemical stability

2M sodium hydroxide, 70% ethanol, 30% isopropanol, 30% acetonitrile, 1% SDS, 6M guanidine hydrochloride, 8M urea

Linear flow velocity (0.3 MPa)

≥250 cm/h

Maximum pressure

0.3 MPa

Storage solution

20% ethanol

Storage conditions

4℃-30℃


Frequently Asked Questions and Solutions


Issue

Possible Causes

Solutions

Rapid increase in chromatographic peak

Overly tight packing of the resin

Repack the column

Slow or tailing chromatographic peak

Loose packing of the resin

Repack the column

Cracks or dryness in the column bed

Leakage or introduction of large air bubbles

Check for leaks or bubbles in the tubing and repack the column if necessary

Poor separation efficiency

1. Inappropriate choice of matrix

Verify if the selected matrix is suitable

2. Poor column performance

Evaluate the column efficiency

3. Oversampling

Optimize the optimal sampling volume

4. Excessive flow rate

Optimize the optimal flow rate

Slow liquid flow

1. Protein or lipid aggregation

Clean the matrix or filter membrane promptly

2. Protein precipitation in the matrix

Adjust the composition of equilibration and elution buffers to maintain the stability of the target substance and the binding efficiency of the matrix

3. Microbial growth in the separation column

Reagents used must be filtered and degassed; samples must be centrifuged or filtered before loading onto the column



Order information


Product

Specification

Item number

Focurose 4FF

25mL

HN030303025M

Focurose 4FF

100mL

HN030303100M

Focurose 4FF

500mL

HN030303500M

Focurose 4FF

1L

HN030303001L

Focurose 4FF

5L

HN030303005L

Focurose 4FF

20L

HN030303020L

 

 



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