70751
BugBuster® Ni-NTA His•Bind® Purification Kit
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| Taglio della confezione | SKU | Disponibilità | Prezzo |
|---|---|---|---|
| 1 kit | Per conoscere la disponibilità, visualizza il carrello | CHF 557.00 |
Informazioni su questo articolo
CHF 557.00
manufacturer/tradename
Novagen®
storage condition
OK to freeze
shipped in
wet ice
General description
Application
Other Notes
•10,000 UBenzonase Nuclease, purity >90%
•10 mlNi-NTA His•Bind Resin
•pkg/4Chromatography Columns
Legal Information
Disclaimer
1 of 1
Questo articolo | |||
|---|---|---|---|
| manufacturer/tradename Novagen® | manufacturer/tradename Novagen® | manufacturer/tradename Novagen® | manufacturer/tradename Chemicon® |
| storage condition OK to freeze | storage condition OK to freeze | storage condition OK to freeze | storage condition - |
| shipped in wet ice | shipped in wet ice | shipped in ambient | shipped in wet ice |
signalword
Warning
hcodes
Classe di stoccaggio
3 - Flammable liquids
wgk
WGK 3
Hazard Classifications
Flam. Liq. 3
Certificati d'analisi (COA)
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Articoli
This article shows the use of BugBuster® and Benzonase® as protein purification tools to extract recombinant proteins from E. coli and to reduce the viscosity of the extract.
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.
E. coli transformation with poly-histidine tagged constructs represents a common vehicle for protein production. Initial screening of small-scale cultures is routinely performed to identify clones producing the highest amounts of protein with the desired form and function. As the demand for greater throughput at this level has increased, so has the need for process simplification and greater reproducibility. To meet this need, we have developed a condensed workflow that can be performed in a single device.
Numero articolo commerciale globale
| SKU | GTIN |
|---|---|
| 369071-5G | 04061837008450 |
| 70751-3 | 04055977273168 |