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I6505

Sigma-Aldrich

Diethylaminoethyl–Sephacel®

aqueous ethanol suspension, 40-160 μm (wet), exclusion limit ~1,000,000 Da

Synonyme(s) :

DEAE-Sephacel®

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About This Item

Numéro CAS:
9013-34-7
Numéro MDL:
MFCD00146622
Code UNSPSC :
47101511
ID de substance PubChem :
24896090
Nomenclature NACRES :
NA.56

Forme

aqueous ethanol suspension

Technique(s)

activity assay: suitable

Taille des particules

40-160 μm (wet)

Dimension de pores

~1,000,000 Da exclusion limit

pH

2—12

Capacité

100-140 μeq/mL, gel

Température de stockage

2-8°C

Chaîne SMILES 

OC[C@@H]1O[C@@H](O[C@H]2[C@@H](O)[C@H](O)[C@@H](O)O[C@H]2CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3?,4?,5?,6?,7?,8?,9?,10-,11?,12+/m1/s1

Clé InChI

GUBGYTABKSRVRQ-WFVLMXAXSA-N

Description générale

I6505-500ML′s update product number is GE17-0500-01

Application

Diethylaminoethyl (DEAE) Sephacel® is used in protein chromatography, ion exchange chromatography, and anion exchange media. It has been used to study sperm motility, sperm capacitation and sperm-oocyte interactions. DEAE Sephacel has also been used to study patients with immunoglobulin A (IgA) nephropathy. Diethylaminoethyl–Sephacel® has been used:

  • in the purification of media samples by ion-exchange chromatography
  • in the isolation of glycosaminoglycans (GAG) from cultured animal cells
  • in the purification of cytotoxic fractions from Tritrichomonas foetus isolates

Forme physique

Suspension in 20% ethanol

Informations légales

Sephacel is a registered trademark of Cytiva

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Flame
GHS02

Mention d'avertissement

Warning

Mentions de danger

H226

Classification des risques

Flam. Liq. 3

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

129.2 °F

Point d'éclair (°C)

54 °C

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

H A Frank et al.
Photosynthesis research, 37(3), 193-203 (1993-09-01)
Triplet state electron paramagnetic resonance (EPR) experiments have been carried out at X-band on Rb. sphaeroides R-26 reaction centers that have been reconstituted with the carotenoid, spheroidene, and exchanged with 13(2)-OH-Zn-bacteriochlorophyll a and [3-vinyl]-13(2)-OH-bacteriochlorophyll a at the monomeric, 'accessory' bacteriochlorophyll
Pierina De Muro et al.
Scandinavian journal of urology and nephrology, 41(3), 230-236 (2007-05-01)
A 2-year follow-up study was carried out in patients with IgA nephropathy (IgAN) in order to verify the possible use of quali-quantitative analysis of urinary glycosaminoglycans (GAGs) as a prognostic index of disease and for drug treatment monitoring. Ten patients
C M Rembold et al.
Biochimica et biophysica acta, 1500(3), 257-264 (2000-03-04)
Nitrovasodilators, high extracellular Mg(2+), and some other relaxing agents can cause smooth muscle relaxation without reductions in myosin regulatory light chain (MRLC) phosphorylation. Relaxations without MRLC dephosphorylation suggest that other regulatory systems, beyond MRLC phosphorylation, are present in smooth muscle.
Daniel R Studelska et al.
Glycobiology, 16(1), 65-72 (2005-09-17)
Glycosaminoglycans (GAGs) are linear polysaccharides made by all animal cells. GAGs bind to hundreds of proteins, such as growth factors, cytokines, chemokines, extracellular matrix components, protease inhibitors, proteases, and lipoprotein lipase, through carbohydrate and protein interactions. These interactions control many
V T D'Souza et al.
Biochemical and biophysical research communications, 129(3), 727-732 (1985-06-28)
An artificial chymotrypsin, with all the features of the real chymotrypsin, namely a binding site (from cyclodextrin) attached to a catalytic site containing an imidazolyl group, a carboxylate group and a hydroxyl group, has been synthesized. This artificial chymotrypsin has
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