Download 1.16891 / 1.16886 Fractogel® EMD COO

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Cell-penetrating peptide wikipedia , lookup

Gene expression wikipedia , lookup

Membrane potential wikipedia , lookup

Mechanosensitive channels wikipedia , lookup

Gel electrophoresis wikipedia , lookup

Theories of general anaesthetic action wikipedia , lookup

Proteasome wikipedia , lookup

G protein–coupled receptor wikipedia , lookup

Immunoprecipitation wikipedia , lookup

Magnesium transporter wikipedia , lookup

SR protein wikipedia , lookup

List of types of proteins wikipedia , lookup

Protein wikipedia , lookup

Protein moonlighting wikipedia , lookup

Nuclear magnetic resonance spectroscopy of proteins wikipedia , lookup

Chromatography wikipedia , lookup

Interactome wikipedia , lookup

Cyclol wikipedia , lookup

Two-hybrid screening wikipedia , lookup

Western blot wikipedia , lookup

Protein–protein interaction wikipedia , lookup

Intrinsically disordered proteins wikipedia , lookup

G protein-gated ion channel wikipedia , lookup

Protein purification wikipedia , lookup

Protein adsorption wikipedia , lookup

QPNC-PAGE wikipedia , lookup

Transcript
1.16891 / 1.16886 Fractogel® EMD COO- (S), (M)
Ion Exchange chromatography using weak cation exchangers
Fractogel® ion exchangers are cross-linked polymethacrylate resins with pore sizes of about 800 Å modified according
to the tentacle technology. The Fractogel® beads have a high mechanical and chemical stability. Since the functional
ion exchanger groups are bonded via linear polymer chains, the ionic groups are accessible for proteins.
Fractogel® EMD COO- is a chromatographic support for the purification of basic and neutral proteins and peptides.
Due to the titration behaviour the ion exchange capacity can be used from pH 6 up to pH 12. 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 COO- when the pH of the buffer is about 1 unit below
their isoelectric points (pl).
The strength of the binding depends on:
the buffer system
pH value of the buffer which determines the surface charge of the protein
the degree of the ionisation of the functional groups of the exchanger
the concentration of the counter ions
the charge density on the support (protein binding capacity)
•
•
•
•
•
Properties of the tentacle ion exchanger
Cat. No.
1.16891, S-Type
1.16886, M-Type
Bulk material
100 ml, 500 ml, 5 l (S)
100 ml, 500 ml, 5 l (M)
Particle size
20 – 40 µm (S)
40 – 90 µm (M)
Type of chromatography
Weak cation exchange chromatography
Functional group
Carboxy ethyl group
Protein binding capacity
100 mg lysozyme/ml of gel
pK value
about 4.5
pH stability range
pH 1 up to pH 12
Elution conditions
High salt concentrations
Pressure limit
8 bar
Operating temperature
4 °C to room temperature
Storage, preservative
20 % ethanol, 150 mmol/l NaCl
Regeneration
1 – 2 M NaCl
Sanitization
0.1 – 0.5 M NaOH, sodium lauroyl sarcosinate
Linear flow rate
Up to 360 cm/h (S-type); up to 400 cm/h (M-type)
Merck KGaA · Life Science Products · Darmstadt · Germany
[email protected] · www.merck-lsp.de
1/1