LSKMAGS08
Supporto magnetico PureProteome
The PureProteome Magnetic Stand is designed to rapidly & easily isolate magnetic particles from up to eight 1. 5 mL or 2. 0 mL tubes.
Sinonimo/i:
Supporto per microsfere magnetiche, Supporto per separazione magnetica
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Informazioni su questo articolo
Vai a
Materiali
self-standing
Caratteristiche
binder
Produttore/marchio commerciale
PureProteome
tecniche
RNA purification: suitable (with magnetic beads)
protein purification: suitable
Condizioni di spedizione
ambient
Categorie correlate
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Questo articolo | LSKMAGS15 | LSKMAG03CBX | LSKMAGL10 |
|---|---|---|---|
| feature binder | feature binder | feature - | feature - |
| manufacturer/tradename PureProteome | manufacturer/tradename PureProteome | manufacturer/tradename PureProteome | manufacturer/tradename PureProteome |
| material self-standing | material self-standing | material - | material - |
| technique(s) RNA purification: suitable (with magnetic beads) | technique(s) RNA purification: suitable (with magnetic beads), protein purification: suitable | technique(s) protein purification: suitable | technique(s) depletion: suitable (serum), protein purification: suitable |
| shipped in ambient | shipped in ambient | shipped in wet ice | shipped in wet ice |
Descrizione generale
Applicazioni
Colture cellulari
Caratteristiche e vantaggi
- Assicura processi riproducibili
- Risultati paragonabili a quelli dei protocolli convenzionali
Esclusione di responsabilità
Certificati d'analisi (COA)
Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.
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Articoli
Vergleich von Elutionstechniken für die Proteinaufreinigung von FLAG® Tag Proteinen im kleinen Maßstab mittels anti-FLAG® M2 Magnetperlen.
Comparison of elution techniques for small-scale protein purification of FLAG® tag proteins using anti-FLAG® M2 magnetic beads.
PureProteome™ Protein A and G Magnetic beads provide a rapid and reproducible means to purify immunoglobulins (IgG) using the KingFisher Duo particle processor.
Contenuto correlato
Immunoprecipitation (IP) is a powerful technique for proteomic screening, biomarker discovery, and signaling network elucidation. It is frequently used to enrich target proteins from complex samples such as cell lysates or extracts. Traditional IP protocols use Protein A, Protein G or a mixture of Protein A and G coupled to a solid support resin, such as agarose beads, to capture an antigen/antibody complex in solution. As the number of samples increase, the traditional, manual IP method can be time-consuming. Processing of multiple IP reactions in parallel can introduce complexity, variability and pipetting errors, which may affect reproducibility.
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