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| you’re in > Products > Manufacturers > Tosoh > TSK-GEL Anion Exchange COLUMNS |
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TSK-GEL Anion Exchange Columns |
- TSKgel Q- and DNA-STAT columns provide high efficiency separations at short analysis time.
- TSKgel DNA-NPR columns are ideal for PCR fragment
analysis.
- TSKgel SuperQ-5PW columns have higher capacity than TSKgel DEAE-5PW due to novel bonding chemistry, effective pore size is smaller for SuperQ-5PW.
- Pore structure and bonding chemistry of TSKgel BioAssist Q
columns provide high capacity for small to very large MW
proteins and nucleic acids.
- BioAssist columns are packed in 4.6 mm ID or 10 mm ID PEEK
hardware. Other columns are available in glass and stainless
steel for analytical, semi-preparative and preparative
applications.
- Binding capacity for small to medium size proteins on TSKgel
DEAE-3SW is roughly double that of the DEAE-5PW due to the
smaller pore size and larger surface area.
- TSKgel DEAE-5PW and DEAE-2SW columns are available in
2 mm ID format for mass spec applications.
- Specialty columns for analysis of mono- and disaccharides
and sugar alcohols are also available.
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| Please click here to see TSK-GEL Anion Exchange Applications. |
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Specialty Columns
Analyses of monosaccharides, disaccharides, and sugar alcohols
can be performed on PS-DVB columns, either by isocratic
(TSKgel Sugar AXI) or by gradient (TSKgel Sugar AXG) analysis.
Saccharides are retained on Sugar AX columns following the
formation of negatively charged complexes with boric acid at
alkaline pH. Figure 7 shows the separation of twelve mono- and
di-saccharides.
The strong anion exchange TSKgel SAX column can be used for
the separation of isomerized sugars, alcohols, and low molecular
weight organic acids. |
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Description |
ID (mm) |
Length (cm) |
Particule Size (μm) |
Number Theoretical Plates |
Flow Rate (mL/min)
|
Max Pressure Drop (kg/cm2)
|
Part # |
| Range |
Max |
| Glass columns |
| DEAE-5PW 1000 Å |
5.0 |
5.0 |
10 |
≥ 700 |
0.5-0.8 |
1.0 |
15 |
13061 |
| DEAE-5PW 1000 Å |
8.0 |
7.5 |
10 |
≥ 1,300 |
0.5-1.0 |
1.2 |
10 |
08802 |
| DEAE-5PW 1000 Å |
20.0 |
15.0 |
13 |
≥ 3,000 |
4.0-6.0 |
8.0 |
15 |
14016 |
| SuperQ-5PW 1000 Å |
8.0 |
7.5 |
10 |
≥ 1,300 |
0.5-1.0 |
1.2 |
20 |
13386 |
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| PEEK Columns |
| BioAssist Q, 4000 Å |
4.6 |
5.0 |
10 |
≥ 500 |
0.3-1.0 |
1.2 |
25 |
19685 |
| BioAssist Q, 4000 Å |
10 |
10.0 |
13 |
≥ 500 |
1.0-5.0 |
7.0 |
25 |
21410 |
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| Stainless steel columns: polymer-based |
| Q-STAT, nonporous |
3.0 |
3.5 |
10 |
≥ 200 |
|
|
100 |
21960 |
| Q-STAT, nonporous |
4.6 |
10.0 |
7 |
≥ 2,000 |
|
|
100 |
21961 |
| Q-STAT, nonporous |
4.6 |
10.0 |
5 |
≥ 4,000 |
|
|
150 |
21962 |
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| DEAE-NPR, nonporous |
4.6 |
3.5 |
2.5 |
≥ 1,300 |
1.0-1.5 |
1.6 |
200 |
13075 |
| DNA-NPR, nonporous |
4.6 |
7.5 |
2.5 |
≥ 6,000 |
0.5-1.0 |
1.5 |
300 |
18249 |
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| QC-PAK GFC 200 |
7.8 |
15 |
5 |
≥ 10,000 |
0.5-1.0 |
1.2 |
40 |
16215 |
| QC-PAK GFC 300 |
7.8 |
15 |
5 |
≥ 10,000 |
0.5-1.0 |
1.2 |
40 |
16049 |
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| DEAE-5PW, 1000 Å |
2.0 |
7.5 |
10 |
≥ 1,300 |
0.05-0.10 |
0.12 |
15 |
18757 |
| DEAE-5PW, 1000 Å |
7.5 |
7.5 |
10 |
≥ 1,300 |
0.5-1.0 |
1.2 |
15 |
07164 |
| DEAE-5PW, 1000 Å |
21.5 |
15.0 |
13 |
≥ 3,000 |
4.0-6.0 |
8.0 |
25 |
07574 |
| DEAE-5PW, 1000 Å |
55.0 |
20.0 |
20 |
≥ 1,500 |
20.0-40.0 |
50.0 |
4 |
07930 |
| SuperQ-5PW, 1000 Å |
7.5 |
7.5 |
10 |
≥ 1,300 |
0.5-1.0 |
1.2 |
20 |
18257 |
| SuperQ-5PW, 1000 Å |
21.5 |
15.0 |
13 |
≥ 3,000 |
4.0-6.0 |
8.0 |
20 |
18387 |
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Sugar AXI,
60 Å |
4.6 |
15.0 |
8 |
≥ 3,700 |
0.2-0.4 |
0.5 |
30 |
08639 |
Sugar AXI,
60 Å |
4.6 |
15.0 |
10 |
≥ 2,700 |
0.2-0.4 |
0.5 |
20 |
08640 |
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| SAX |
6.0 |
15.0 |
5 |
≥ 2,000 |
0.5 - 1.0 |
1.2 |
150 |
07157 |
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| Stainless steel columns: silica-based |
| DEAE-2SW, 125 Å |
2.0 |
25.0 |
5 |
≥ 5,000 |
0.12-0.17 |
0.22 |
130 |
18761 |
| DEAE-2SW, 125 Å |
4.6 |
25.0 |
5 |
≥ 5,000 |
0.6-0.8 |
1.0 |
150 |
07168 |
| DEAE-3SW, 250 Å |
7.5 |
7.5 |
10 |
≥ 1,300 |
0.5-1.0 |
1.2 |
20 |
07163 |
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| Guard column products |
| DEAE-NPR |
4.6 |
0.5 |
5 |
Guard column for P/N 13075 |
17088 |
| DNA-NPR |
4.6 |
0.5 |
5 |
Guard column for P/N 18249 |
18253 |
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| SuperQ-5PW |
|
|
20 |
Guardgel Kit for P/N 18257 |
18388 |
| SuperQ-5PW |
|
|
20 |
Guardgel Kit Glass for P/N 18386 |
18389 |
| SuperQ-5PW |
|
|
20 |
Guardgel Kit for P/N 18387 |
18390 |
| |
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| DEAE-5PW |
|
|
20 |
Guardgel Kit for P/N 18257 |
07210 |
| DEAE-5PW |
2.0 |
1.0 |
10 |
Guard cartridge for P/N 18757 |
42152 |
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| DEAE-5PW |
|
|
20 |
Guardgel Kit Glass for P/N 13061 and 08802 |
08806 |
| DEAE-5PW |
20 |
2.0 |
13 |
Guard column Glass for P/N 14016 |
14466 |
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| DEAE-5PW |
|
|
20 |
Guardgel Kit Prep for P/N 07574 |
16092 |
| DEAE-5PW |
45 |
5.0 |
20 |
Guard column for P/N 07930 |
07928 |
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| DEAE-SW |
|
|
20 |
Guardgel Kit for P/N 07168 and 07163 |
07648 |
| DEAE-2SW |
2.0 |
1.0 |
5 |
Guard cartridge for P/N 18761 |
42154 |
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| Guard cartridge holder(2.0mm ID, 1.5cm L) |
For all 2mm ID guard cartridges |
19308 |
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| Applications |
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Nonporous TSKgel STAT Anion Exchange Columns
STAT columns are available in various column formats and particle sizes to perfectly match specific application needs. For fast and ultra-fast analysis anion and cation exchange columns in 3 mm ID and 3.5 cm length are packed with 10 µm particles.
They are ideally suited for rapid candidate screening or process monitoring. 4.6 mm ID and 10 cm length columns packed with 7 µm particles are designed for high resolution IEC separation for example for the separation of nucleic acids, mAb variants, PEGylated protein or protein aggregates.
Figure 1 compares the high resolution separation of nucleotides on a 10 cm length column to the high throughput separation on a 3.5 cm length column (analysis performed on prototype columns). Polymer-based Anion Exchange Columns. |
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Figure 1 |
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BioAssist Q TSKgel
BioAssist Q is suitable for use in systems that are designed for laboratory or semi-preparative applications. Figure 2 demonstrates the performance enhancement of TSKgel BioAssist Q over a competitive product when operated side-byside on an FPLC system. TABLE I shows typical dynamic binding capacities on BioAssist Q relative to competitive products.
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Table 1 |
Figure 2 |
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SuperQ-5PW and DEAE-5PW
Figure 3 shows the analysis of a 16-mer morpholine oligonucleotide on TSKgel SuperQ-5PW column using a NaCl gradient in a 10 mmol/L sodium hydroxide mobile phase. Figure 4 shows the fractionation of high molecular weight E. coli RNA on TSKgel DEAE-5PW, effectively utilising the large 1000 Å pores of this base resin. |
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Figure 3 |
Figure 4 |
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DEAE-NPR and DNA-NPR
Because of their small (2.5 µm) particle size, non porous resin (NPR) columns excel in rapid separations of large biomolecules such as DNA digests.
A chromatogram of a standard Hae III digest of pBR322 DNA on TSKgel DEAE-NPR, protected by a guard column, is shown in Figure 5.
To achieve better resolution for PCR fragment analysis we recommend the use of TSK-GEL DNA-NPR columns, which are 7.5 cm long and 4.6 mm wide, providing higher efficiency in a longer column. |
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Figure 5 |
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Silica-based Anion Exchange Columns
TSK-GEL 2SW-type columns provide high performance separations of small ionic solutes. The increased solubility of the silica backbone above pH 7 limits the use of the TSK-GEL 2SWtype columns to acidic or neutral mobile phases. This restricts method development and requires special cleaning procedures when compared to the more robust TSK-GEL 5PW-type polymerbased columns.
High performance analyses of small anionic species are best performed on small pore silica-based anion exchangers, such as TSKgel DEAE-2SW. This is demonstrated in Figure 6. The 250 Å pore size TSKgel DEAE-3SW column is used for separating peptides, low MW proteins and DNA fragments. |
Specialty Columns
Analyses of monosaccharides, disaccharides, and sugar alcohols can be performed on PS-DVB columns, either by isocratic (TSKgel Sugar AXI) or by gradient (TSKgel Sugar AXG) analysis. Saccharides are retained on Sugar AX columns following the formation of negatively charged complexes with boric acid at alkaline pH.
Figure 7 shows the separation of twelve mono- and di-saccharides. The strong anion exchange TSKgel SAX column can be used for the separation of isomerized sugars, alcohols, and low molecular weight organic acids. |
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Figure 6 |
Figure 7 |
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