UltraPure™ 10x TBE Buffer ist eine steril filtrierte Lösung aus 1 M Tris, 0,9 M Borsäure und 0,01 M EDTA,Weitere Informationen
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Katalognummer
Menge
15581028
10 l
15581044
1 l
2 Optionen
Katalognummer 15581028
Preis (EUR)
213,00
Each
Menge:
10 l
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
213,00
Each
UltraPure™ 10x TBE Buffer ist eine steril filtrierte Lösung aus 1 M Tris, 0,9 M Borsäure und 0,01 M EDTA, die zur Herstellung von 1x Puffer für die Polyacrylamid- und Agarose-Gelelektrophorese verwendet wird. UltraPure™ 10X TBE- uffer ist in einer 1 l-Kunststoffflasche oder in einer 10 l-Cubitainer™ Box erhältlich.
Leistungs- und Qualitätskontrolle Es wurde keine DNase-, RNase- oder Protease-Aktivität festgestellt.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
PufferLaufpuffer
Konzentration10 X
Zur Verwendung mit (Anwendung)Nukleinsäure-Gelelektrophorese, Blotting
GelkompatibilitätPolyacrylamid-Gele, Agarose-Gele
ProduktlinieUltraPure
ProdukttypTBE-Puffer
Menge10 l
VersandbedingungRaumtemperatur
FormatFlasche
Unit SizeEach
Inhalt und Lagerung
Bei Raumtemperatur lagern.
Häufig gestellte Fragen (FAQ)
Can I autoclave agarose to prepare agarose gels?
No. Autoclaving at temperatures that are too high or pressures that are too high can hydrolyze the agarose polymer and weaken it.
Do you have any tips for preparing high-percentage (3% to 4%) agarose gels?
Add the powder to cold buffer while stirring. Let the agarose rehydrate for 1 to 2 hr and then heat slowly until agarose is completely dissolved. Using a microwave at low power settings is acceptable.
What can I do to prevent static on agarose bottles?
One recommendation: get a supply of fabric softener sheets and wipe the bottle with a sheet before opening it.
How can I avoid the build-up of the precipitous film sometimes seen in 10X TBE?
The precipitation of concentrated TBE stocks may be due to nucleation of salt crystals by dust particles or other insoluble materials. Therefore, filtering the solution through a 0.2 µm cellulose acetate or cellulose nitrate filter after preparation helps avoid this precipitate. [Mayeda A, Krainer A (1991) BioTechniques 10.2, 1820]
How can generation of replication competent adenoviruses be avoided when using your pSilencer adeno 1.0-CMV System?
Although there is only a very small chance of creating replication competent virus, steps should still be taken to avoid added risk. The virus is expanded in two rounds of amplification, and all secondary expansions should be performed from an initial expansion stock. Secondary amplifications in HEK293 cells should not be performed from the stock of another secondary expansion, as this could increase the chance of making replication competent virus. See the product manual for more detail and guidelines for screening.
Find additional tips, troubleshooting help, and resources within our RNAi Support Center.