CL6B200
Sepharose™ CL-6B Size Exclusion Resin
Cross-linked, 90-350 mesh
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product name
Sepharose™ CL-6B, Cross-linked
Quality Level
form
suspension
bead diameter
40-165 μm
pore size
10,000-1,000,000 fractionation range (Dextrans)
10,000-4,000,000 fractionation range (Globular proteins)
storage temp.
2-8°C
Related Categories
General description
Sepharose CL is a cross-linked derivative of sepharose, prepared by reacting sepharose with 2,3-dibromopropanol under strongly alkaline conditions.
Application
Sepharose CL-6B is used in affinity chromatography, protein chromatography, gel filtration chromatography, separation media and resins. Sepharose™ CL-6B has been used to study in vitro inhibition of human melanoma cells and to gather data in other valuable anticancer studies.
Sepharose™CL-6B has been used for the purification of glucoamylase enzyme and targeted ribonucleoprotein (RNP).
Legal Information
Sepharose is a trademark of Cytiva
replaced by
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Certificates of Analysis (COA)
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A membrane-associated ATPase with an M(r) of approximately 510,000 and containing subunits with M(r)s of 80,000 (alpha), 55,000 (beta), and 25,000 (gamma) was isolated from the methanogen Methanococcus voltae. Enzymatic activity was not affected by vanadate or azide, inhibitors of
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Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica, 30(6), 561-564 (2002-08-09)
Luffin B, a plan single-chain ribosome inactivating protein, was purified from seeds of Luffa cylindrica by Blue Sepharose CL-6B affinity chromatography. An immunotoxin was constructed with luffin B and Ng76, a monoclonal antibody to human melanoma cell M(21). Luffin B-Ng76
Eric Bertoft et al.
International journal of biological macromolecules, 49(4), 441-453 (2011-06-28)
The unit chains of amylopectin are organized into clusters. In this study, the cluster structure was analysed in detail in four different genotypes of barley, of which two possessed the amo1 genetic background. Amylose content of the barley starches differed
Carla Cruz et al.
Journal of molecular recognition : JMR, 24(6), 975-980 (2011-11-01)
The binding between four matrices (beaded cellulose, cellulose acetate, cellulose triacetate and Sepharose CL-6B) and beaded cellulose derivatized with a thiacarbocyanine dye with 5'-mononucleotides is investigated by Saturation Transfer Difference Nuclear Magnetic Resonance (STD-NMR) technique. This procedure intends to identify
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