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
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
Traditionally, protein purification from E. coli consists of four distinct phases: harvest, bacterial cell lysis, lysate clarification and protein purification. Bacterial lysis typically requires several time-consuming, hands-on steps, such as freeze/thaw cycles and sonication. These harsh lysis techniques may negatively impact protein quality and contribute to sample-to-sample variability. To maintain protein activity and integrity, detergent-based lysis buffers are routinely used to avoid mechanical protein extraction methods. Regardless of the lysis method used, centrifugation is traditionally required to pellet unwanted cell debris and permit recovery of the clarified lysate. The final step, purification, is frequently performed using affinity media specific for expressed epitope tags. Agarose-based media have typically been used, either as a slurry in microcentrifuge tubes or packed into gravity-driven or spin columns. While easier to manipulate, columns are greatly affected by lysate consistency and carryover of cell debris, which can lead to clogging of the column frits.
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