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Merck

H9914

Millipore

HIS-Select® Nickel Magnetic Agarose Beads

Synonym(e):

nickel charged magnetic beaded agarose

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1 ML
CHF 169.00
5 ML
CHF 670.00

CHF 169.00


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1 ML
CHF 169.00
5 ML
CHF 670.00

About This Item

UNSPSC-Code:
41106500
NACRES:
NA.56

CHF 169.00


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Bulk-Bestellung anfordern

Konjugat

magnetic beads

Form

suspension

Haltbarkeit

2 yr (Unopened product)

Matrix

6% beaded magnetic agarose

Kapazität

≥15 mg/mL binding capacity

Lagertemp.

2-8°C

Allgemeine Beschreibung

HIS-Select Magnetic Agarose Beads consist of paramagnetic, immobilized metal-ion affinity chromatography (IMAC) resin that contain a proprietary quadridentate chelate, which is bound with nickel and covalently attached through a non-charged, hydrophilic linker to magnetic beaded agarose. The magnetic properties of the beads aid in manipulations, such as repetitive washings, and recovery of the protein bound beads. This leads to greater experimental reproducibility and more accurate quantitation of the His-tagged proteins of interest.

Anwendung

The HIS-Select Nickel Magnetic Agarose Beads are designed for use in automated and small-scale affinity capture (molecular pull-down) purifications of histidine-tagged protein / His-tag protein while exhibiting low non-specific binding of other proteins. The beads can be used to purify His-tagged proteins under native and denaturing conditions.

Physikalische Form

Supplied as a 50% slurry suspension in 30% Ethanol.

Rechtliche Hinweise

HIS-Select is a registered trademark of Merck KGaA, Darmstadt, Germany

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Aquatic Chronic 3 - Carc. 1B - Flam. Liq. 3 - Repr. 1B - Skin Sens. 1 - STOT RE 2

Zielorgane

Respiratory Tract

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

86.0 °F

Flammpunkt (°C)

30 °C


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Sonja Hänzelmann et al.
Clinical epigenetics, 7, 19-19 (2015-03-13)
Primary cells enter replicative senescence after a limited number of cell divisions. This process needs to be considered in cell culture experiments, and it is particularly important for regenerative medicine. Replicative senescence is associated with reproducible changes in DNA methylation
Mei Suen Kong et al.
Science signaling, 12(567) (2019-02-07)
T cell activation is initiated by signaling molecules downstream of the T cell receptor (TCR) that are organized by adaptor proteins. CIN85 (Cbl-interacting protein of 85 kDa) is one such adaptor protein. Here, we showed that CIN85 limited T cell
Philip Vitorino et al.
Nature, 519(7544), 425-430 (2015-03-25)
Cell migration is a stepwise process that coordinates multiple molecular machineries. Using in vitro angiogenesis screens with short interfering RNA and chemical inhibitors, we define here a MAP4K4-moesin-talin-β1-integrin molecular pathway that promotes efficient plasma membrane retraction during endothelial cell migration.
Joshua W Burgess et al.
American journal of respiratory cell and molecular biology, 41(6), 714-721 (2009-03-17)
Pneumocystis organisms are opportunistic fungal pathogens that cause significant pneumonia in immune-compromised hosts. Recent evidence has suggested that Pneumocystis carinii exists as separate mating types, and expresses and regulates proteins that govern meiosis and progression of the life cycle. This
Yun Wei et al.
Journal of materials chemistry. B, 1(15), 2066-2071 (2013-04-21)
The imidazolium cation was chosen as protein selective affinity group and a kind of ionic liquid magnetic microspheres was developed by immobilizing imidazolium cations onto the surface of silica-coated magnetic microspheres to form imidazolium ionic liquid modified magnetic microspheres (Fe3O4@SiO2@IL).

Verwandter Inhalt

Protein purification techniques, reagents, and protocols for purifying recombinant proteins using methods including, ion-exchange, size-exclusion, and protein affinity chromatography.

Proteinaufreinigungsverfahren, Reagenzien und Protokolle zur Aufreinigung rekombinanter Proteine unter Anwendung von Methoden wie Ionenaustausch, Größenausschluss und Proteinaffinitätschromatographie.

Proteinexpressionstechnologien für verschiedene Expressionssysteme zur Unterstützung von Forschung und der Herstellung von Arzneimitteln und Impfstoffen.

Protein expression technologies for various expression systems supporting research, therapeutics, and vaccine production.

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