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| L00432-1 | |
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| 咨询产品问题 | |
| Product Description |
GenScript Anti‐DYKDDDDK G1 Affinity Resin
(Cat. No. L00432) is designed for the purification of DYKDDDDK‐tagged protein
from commonly used protein expression systems including bacteria, yeast and mammalian
cells. |
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| Key Features |
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| Product Content |
50% settled resin in TBS with 0.02% sodium azide |
| Matrix |
4% cross‐linked agarose |
| Average Bead size |
90 μm |
| Ligand |
Mouse monoclonal antibody against DYKDDDDK tag, clone G1 |
| Binding Capacity |
Approximately 1.5 mg DYKDDDDK‐tagged protein per ml settled resin |
| Elution Method |
Acid, alkaline, neutral, peptide competitive or SDS‐PAGE loading buffer elutions* (*If elute with SDS-PAGE loading buffer, the heavy chain of G1 antibody will be denatured and release from the resin.) |
| Resin Reuse |
The resin can be recycled for at least 4 times. If maintained properly, the
resin can be reused 10 times with minimum loss of binding capability. |
| Reagents Compatibility |
Compatible with commonly used reagents at certain concentrations |
| Storage & Stability | This product is stable for 1 year if stored at 2°C~8°C from the date of manufacture. Do not store at 0°C or below 0°C to avoid freezing the resin. |
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Figure 1.
Purification of
DYKDDDDK‐tagged protein from E. coli lysate
Lanes:
1. Whole cell lysate
2. Flow through
3. Protein marker
4‐8. Eluate of target DYKDDDDK‐tagged protein (M.W. 60.4 kDa)
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Figure 2.
Purification of N‐ terminus and Cterminus
DYKDDDDK ‐tagged
proteins
Lanes:
1‐2．Eluate of N‐terminus DYKDDDDKtagged protein (M.W. 19.2 kDa)
3. Protein marker
4‐5. Eluate of C‐terminus DYKDDDDKtagged protein (M.W. 26.4 kDa)
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Figure 3.
Purification of
DYKDDDDK‐tagged protein from mammalian cells
Lanes:
1. Protein marker
2. Supernatant from cultured CHO cells
3. Flow through after binding
4. Eluate of target DYKDDDDK ‐tagged protein (M.W. 27.6 kDa)
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Figure 4.
Purification of
DYKDDDDK‐tagged glycoprotein from mammalian cells
The upper figure shows SDS‐PAGE analysis result and the lower figure shows Western blot result.
Lanes:
1. Protein marker
2. Supernatant from CHO cells expressing target glycoprotein
3. Flow through after binding
4. Eluate of target DYKDDDDK‐tagged protein (M.W. 50.0 kDa)
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Figure 5.
Purification of
DYKDDDDK‐tagged proteins using different elution methods.
Lanes:
1. Protein #1 (M.W. 16.8 kDa) by competitive elution using 300 μg/ml DYKDDDDK peptide.
2. Protein #2 (M.W. 54.6 kDa) by neutral elution with 3M NaCl
3. Protein #3 (M.W. 27.6 kDa) by acid elution, pH 3.5
4. Protein #1 (M.W. 16.8 kDa) by alkaline elution, pH 10.5
5. Protein #1 (M.W. 16.8 kDa) by alkaline elution, pH 12
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Figure 6.
Benchmark with
Sigma‐Aldrich’s
ANTI‐FLAG M2
Affinity Gel
Side‐by‐side comparison of DYKDDDDKtagged protein purification with GenScript’s Anti‐DYKDDDDK G1 Affinity
Resin and Sigma‐Aldrich’s ANTI‐FLAG M2 Affinity Gel, from same staring material following manufacturer suggested procedures.
Lanes:
1. Protein marker
2. Purification from M2 gel (pH 3.5 elution)
3. Purification from G1 resin (pH 12.0 elution)
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