추천 제품
제품명
Sepharose™ CL-6B, Cross-linked
Quality Level
양식
suspension
비드(bead) 직경
40-165 μm
공극 크기
10,000-1,000,000 fractionation range (Dextrans)
10,000-4,000,000 fractionation range (Globular proteins)
저장 온도
2-8°C
일반 설명
Sepharose CL is a cross-linked derivative of sepharose, prepared by reacting sepharose with 2,3-dibromopropanol under strongly alkaline conditions.
애플리케이션
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).
법적 정보
Sepharose is a trademark of Cytiva
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Hiroshi Tomoda et al.
Analytical biochemistry, 311(1), 50-56 (2002-11-21)
The galabiose structure Galalpha1-4Gal is rarely found in natural glycoproteins, but is abundantly present in pigeon egg white proteins as Galalpha(1-4)Galbeta(1-4)GlcNAc termini. Pigeon ovalbumin, ovomucoid, or the whole egg white were immobilized on periodate-oxidized Sepharose CL-6B gels by reductive amination.
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
Mrinal Kumar Das et al.
International journal of biological macromolecules, 49(5), 1096-1103 (2011-09-21)
Articulatin-D, a 66 kDa ribosome inactivating protein (RIP) comprised of 29 kDa A-chain linked to 35 kDa B-chain, is purified from leafless mistletoe (Viscum articulatum) parasitic on Dalbergia sp. from Western Ghats (India). N-terminal sequence and LC-MS/MS analyses of A-
Preparation and Mammalian Plasma Membranes, 7 (1979)
N Vinay Kumar et al.
Methods (San Diego, Calif.), 32(4), 389-397 (2004-03-09)
Intracellular signaling by protein kinases controls many aspects of cellular biochemistry and physiology. Determining the direct substrates of protein kinases is important in understanding how these signaling enzymes exert their effect on cellular functions. One of the recent developments in
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