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ligand
diethyl-(2-hydroxypropyl)aminoethyl
品質水準
物質
polypropylene housing
製品種目
Fractogel®
形状
prepacked column
パラメーター
≤8 bar pressure
~170 cm/hr max. flow rate
column I.D. × L
8 mm × 100 mm
容量
5 mL
マトリックス活性基
Methacrylate
平均粒径
40-90 μm
キャパシティ
~100 mg, BSA binding capacity
アプリケーション
gene therapy
recombinant protein
vaccine development
分離法
anion exchange
保管温度
15-25°C
詳細
Weak cation exchange Fractogel® EMD DMAE (M) resin in a convenient pre-packed 5ml column
特徴および利点
MiniChrom Column Fractogel® DMAE (M), 5 ml enables:
Due to the titration behavior, the ion exchange capacity can be used from pH 2 to pH 9.5. The separation of proteins is based on reversible electrostatic interactions between the negatively charged regions of the proteins′ surface and the support. Proteins are retained efficiently on Fractogel® EMD DEAE when the pH of the buffer is about 1 unit above their isoelectric points (pl).
The strength of the binding depends on the following:
- Excellent binding to large viruses and plasmid DNA
- Homogenous binding with high selectivity and purity
- Lower elution volumes for the highest purity levels
- Compatibility with 2.5 % (v/v) aqueous benzyl alcohol containing 150 mM NaCl storage solution
Due to the titration behavior, the ion exchange capacity can be used from pH 2 to pH 9.5. The separation of proteins is based on reversible electrostatic interactions between the negatively charged regions of the proteins′ surface and the support. Proteins are retained efficiently on Fractogel® EMD DEAE when the pH of the buffer is about 1 unit above their isoelectric points (pl).
The strength of the binding depends on the following:
- the buffer system
- pH value of the buffer which determines the surface charge of the protein
- the degree of the ionization of the functional groups of the exchanger
- the concentration of the counter ions
- the charge density on the support (protein binding capacity)
法的情報
FRACTOGEL is a registered trademark of Merck KGaA, Darmstadt, Germany
試験成績書(COA)
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