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A6017

Sigma-Aldrich

ω-Aminohexyl–Agarose

saline suspension

Sinonimo/i:

Omega-Aminohexyl-Agarose, 1,6-Diaminohexane–Agarose (N-linked), 6-Aminohexyl–Agarose

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10 ML
155,00 €
50 ML
586,00 €
100 ML
952,00 €

155,00 €

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Cambia visualizzazione
10 ML
155,00 €
50 ML
586,00 €
100 ML
952,00 €

About This Item

Numero CAS:
58856-73-8
Numero MDL:
MFCD00801286
Codice UNSPSC:
23151817
NACRES:
NA.56

155,00 €

Per informazioni sulla disponibilità, contatta il Servizio Clienti.

Origine biologica

plant

Stato

saline suspension

Grado di funzionalizzazione

≥5 μmol per mL

tecniche

affinity chromatography: suitable

Matrice

cross-linked 4% beaded agarose

Attivazione matrice

cyanogen bromide

Gruppi immobilizzati alla matrice

amino of 1,6-diaminohexane

Braccio spaziatore

1 atom

Capacità

≥5 mg/mL binding capacity (bovine serum albumin)

Compatibilità

suitable for chromatography

Temperatura di conservazione

2-8°C

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Descrizione generale

Hydrophobic ligands can serve as potentselective adsorbents. Both ω-aminoalkyl and alkyl agaroses can interact with the hydrophobic regions found in various proteins. The ω-aminoalkyl agarose product offered here consists of activated agarose with 1,6-diaminohexane covalently attached to one of its amine groups.

Applicazioni

ω-Aminohexyl–Agarose has been used in the conjugation of fatty acids with chain length from two carbons to 20 for fatty acyl beads pull-down experiments.
ω-aminohexyl–agarose has been used for coupling of serotype b-specific carbohydrate antigen (SbAg) of Actinobacillus actinomycetemcomitans Y4 for isolation of anti-SbAg antibodies using protein chromatography.[1]

Azioni biochim/fisiol

ω-aminoalkyl-agaroses are used in chromatography. In these, the protein is retained by lipophilic association between the hydrocarbon side chains on the agarose and hydrophobic pockets in the protein.[2]

Stato fisico

Suspension in 0.5 M NaCl containing preservative

Altre note

For R&D use only. Not for drug, household, or other uses. Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H315,H318

Classi di pericolo

Eye Dam. 1 - Skin Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificati d'analisi (COA)

Lot/Batch Number
0000431410
0000431410
0000362926
0000362927
0000348305

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S Mandjiny et al.
Journal of chromatography, 616(2), 189-195 (1993-07-02)
Histidine, a pseudobiospecific ligand, had been utilized to purify several proteins such as chymosin, acidic protease, carboxypeptidase Y and immunoglobulin G (IgG). A detailed study was undertaken to purify IgG on histidine coupled to aminohexyl Sepharose [A. El-Kak and M.
L G Martini et al.
Pharmaceutical research, 12(11), 1786-1790 (1995-11-01)
The purpose of this study was to investigate the influence of hydration characteristics on the in vitro release of 5-fluorouracil from a swellable matrix prepared using a novel triblock copolymer of poly(epsilon-caprolactone) and poly(oxyethylene). Matrices were prepared by dry compression
Y Ruttyn et al.
Journal of chromatography, 491(2), 299-308 (1989-07-21)
Human plasma was chromatographed under different experimental conditions on aminohexyl Sepharose. A strong retention of factor VIII/vWf and of factors VII, II, IX and X was observed. A satisfactory stabilization of eluted factor VIII clotting activity was obtained after addition
D Couchie et al.
The Biochemical journal, 199(2), 441-446 (1981-11-01)
Chromatography on hexyl-agarose resolved a partially purified cyclic GMP-activated phosphodiesterase from rat liver into two peaks of activity: the first was eluted with 0.5 M-KCl and was cyclic AMP-specific. The second was tightly bound to hexyl-agarose and was not eluted
Hydrophobic chromatography: use for purification of glycogen synthetase.
Shaltiel S and Er-El Z
Proceedings of the National Academy of Sciences of the USA, 70, 778-781 (1973)
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