产品名称
HiTrap® Q High Performance, Cytiva 17-1154-01, pack of 5 × 5 mL
form
prepacked column
crosslinking
cross-linked
mol wt
protein Mr 10 MDa (exclusion limit)
packaging
pack of 5 × 5 mL
manufacturer/tradename
Cytiva 17-1154-01
storage condition
(20% ethanol)
parameter
20 mL/min max. flow rate
42 psi
5 mL/min flow rate (recommended)
technique(s)
liquid chromatography (LC): suitable
bed volume
5 mL
column I.D. × L
16 mm × 25 mm
matrix
cross-linked agarose, spherical
matrix active group
-CH2N+(CH3)3, quaternary ammonium
particle size
24-44 μm
avg. part. size
34 μm
cleaning
2-14
working range
2-12
capacity
~ 70 mg BSA/mL resin binding capacity
0.14-0.2 mmol Cl-/mL ion exchange capacity
separation technique
anion exchange
shipped in
ambient
storage temp.
2-30°C
Analysis Note
Application
Features and Benefits
- 34 μm bead size for high-performance, high-resolution purifications.
- Convenient and reproducible for fast, easy, high-performance separations either alone or connected in series.
- Designed for use with a syringe, peristaltic pump, and chromatography systems such as AKTA design.
- Strong quaternary ammonium (Q) anion exchanger
General description
Other Notes
Preparation Note
Legal Information
signalword
Warning
hcodes
存储类别
3 - Flammable liquids
法规信息
商品
This page covers detailed aspects of each step in an IEX separation to improve resolution and overall performance.
This page covers practical problems that may lead to a non-ideal IEX separation and their solutions.
This page shows how to perform a purification of His-tagged membrane proteins.
This page covers the standard ÄKTAdesign configurations for simple IEX chromatography.
实验方案
Ion exchange chromatography and Superdex column analysis facilitate protein refolding with step-by-step guidance.
This page covers the use of Sepharose High Performance media for purification of proteins, peptides or oligonucleotides, when to use them, and with which systems.
This page shows how to condition membrane proteins for further analysis with products from Cytiva.
This page clarifies sample preparation, buffer exchange and desalting, removal of lipoproteins, phenol red, and low molecular weight contaminants in Ion exchange chromatography.
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