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Bio-Rad Media Sampler Pack User Manual

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Section 1
Introduction

UNOsphere Q and S ion exchange media are hydrophilic spherical polymeric beads
designed for the separation of proteins, nucleic acids, viruses, plasmids, and other
macromolecules. The UNOsphere beads are designed for high capacity, low
backpressure, and high productivity.

Section 2
Technical Description

Table 1. Characteristics of UNOsphere Media.

UNOsphere Q

UNOsphere S

Type of ion exchanger

Strong anion

Strong cation

Functional group

–N+(CH3)3

–SO3

Total ionic capacity

120 µeq/ml

260 µeq/ml

Dynamic binding capacity*

150 cm/hr

180 mg/ml

60 mg/ml

600 cm/hr

125 mg/ml

30 mg/ml

Shipping counterion

Cl–

Na+

Median particle size

120 µm

80 µm

Recommended linear flow rate range**

50–1,200 cm/hr

50–1,200 cm/hr

Chemical stability

1.0 M NaOH (20°C)

≤2,000 hr

≤2,000 hr

1.0 M HCl (20°C)

≤200 hr

≤200 hr

Volume changes

pH 4–10

<5%

<5%

0.01–1.0 M NaCl

<5%

<5%

Gel bed compression ratio***

25% ± 3%

25% ± 3%

pH stability

1–14

1–14

Autoclavability (121ºC, 30 min)

Yes

Yes

Antimicrobial agent

20% ethanol

20% ethanol

Regeneration

70% ethanol or 1–2 M NaCl

70% ethanol or 1–2 M NaCl

Storage conditions

20% ethanol or 0.1 M NaOH

20% ethanol or 0.1 M NaOH

*10% breakthrough capacity determined with 4.5 mg/ml human IgG (UNOsphere S) and 2.0 mg/ml BSA

(UNOsphere Q) in a 1.1 x 20 cm column.

**UNOsphere media packed to a 20 cm bed height and run at 1,200 cm/hr generate less than 2 bar

backpressure.

***A compression ratio is for axially compressed columns packed at a constant flow rate (100–1,200 cm/hr) or

constant pressure of 1–2 bar. Gel bed will rebound to its original volume 15–20 min after the pump stops.
Columns with small ID may not rebound to original volume due to Wall effects.

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