SYBR™ Safe DNA Gel Stain in 0.5X TBE
Invitrogen™

SYBR™ Safe DNA Gel Stain in 0.5X TBE

SYBR Safe DNA-Gel-Färbemittel wurde speziell für eine verringerte Mutagenität – entwickelt, um mehr Sicherheit für das Färben von DNA inWeitere Informationen
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KatalognummerMenge
S331001 l
S331014 l
Katalognummer S33100
Preis (EUR)
235,00
Each
Menge:
1 l
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
235,00
Each
SYBR Safe DNA-Gel-Färbemittel wurde speziell für eine verringerte Mutagenität – entwickelt, um mehr Sicherheit für das Färben von DNA in Agarose- oder Acrylamid-Gelen zu bieten als Ethidiumbromid. SYBR Safe Färbemittel ist nicht nur weniger mutagen als Ethidiumbromid, sondern die Nachweisempfindlichkeit von SYBR Safe Färbemittel ist besser als die von Ethidiumbromid. SYBR Safe Färbemittel wird als vorgemischte Lösung geliefert, die wie eine Ethidiumbromidlösung verwendet werden kann, entweder im Gel während des Elektrophoreselaufs oder als Nachlauffärbung. Nach Bindung an Nukleinsäuren hat das grün fluoreszierende SYBR Safe Färbemittel Fluoreszenzanregungsmaxima von ∼280 und ∼502 nm und ein Emissionsmaximum von ∼530 nm. SYBR Safe DNA-Gelfärbung ist auch als 1 l (S-33100) gebrauchsfertige Lösung erhältlich. Das SYBR Safe DNA-Gelfärbe-Starterkit (S-33110) enthält 1 l SYBR Safe DNA-Gel-Färbemittel und einen fotografischen Filter (S-37100).

Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.

Specifications
DetektionsstelleIn-Gel-Detektion
NachweisverfahrenFluoreszenz
Menge1 l
Haltbarkeit6 Monate
VersandbedingungRaumtemperatur
ZielmolekülDNA
Marker oder FarbstoffSYBR-sicher
ProdukttypDNA-Gelfärbemittel
Unit SizeEach
Inhalt und Lagerung
• Geliefert als gebrauchsfertige Lösung in 0,5X TBE

Lagerung bei Raumtemperatur im Originalbehälter.

Häufig gestellte Fragen (FAQ)

Why do I sometimes see speckles in my gel when using SYBR Safe DNA Gel Stain?

Many whitening agents used in clothing, as well as some fungi and bacteria, fluoresce at the same wavelengths as SYBR Safe DNA gel stain. These contaminants within or on the surface of the gel may produce this speckling.

What is the pH range of SYBR dyes?

The SYBR dyes are useful only over a narrow range of pH, from about 7 to 8. Outside this range, the fluorescent signal diminishes rapidly.

Which direction does the SYBR Safe dye run during electrophoresis?

Similarly to ethidium bromide, SYBR Safe DNA Gel Stain runs in the opposite direction of the migrating DNA. This has no practical effect on the use of gels cast with SYBR Safe DNA Gel Stain, as only the very bottom of the gel will have a lower concentration of stain. This effect can be partially counteracted by staining the gel with SYBR Safe DNA Gel Stain after electrophoresis. Solutions of dye should not be added to the running buffer as this can cause breakdown of the dye at the electrodes and release toxic volatile compounds into the air.

Does ethanol precipitation remove the SYBR Safe dye?

SYBR Safe DNA Gel Stain is easily removed from nucleic acids by ethanol precipitation.

Can I reuse SYBR Safe DNA Gel Stain for a second gel?

We strongly discourage the reuse of SYBR Safe DNA Gel Stain, as this practice significantly lowers sensitivity.

Zitierungen und Referenzen (11)

Zitierungen und Referenzen
Abstract
Features of medullary thymic epithelium implicate postnatal development in maintaining epithelial heterogeneity and tissue-restricted antigen expression.
Authors:Gillard GO, Farr AG
Journal:J Immunol
PubMed ID:16670287
'Although putative thymic epithelial progenitor cells have been identified, the developmental potential of these cells, the extent of medullary thymic epithelium (mTEC) heterogeneity, and the mechanisms that mediate the expression of a wide range of peripheral tissue-restricted Ags (TRAs) by mTECs remain poorly defined. Here we have defined several basic ... More
Biotinylated photocleavable polyethylenimine: capture and triggered release of nucleic acids from solid supports.
Authors:Handwerger RG, Diamond SL
Journal:Bioconjug Chem
PubMed ID:17432825
'A biotinylated photocleavable polyethylenimine (B-PC-PEI) was designed and synthesized for the capture and controlled release of nucleic acids from solid supports. B-PC-PEI was synthesized via a three-step reaction process and verified by 1H NMR and mass spectrometry. In aqueous solution, the o-nitrobenzyl group within B-PC-PEI was efficiently cleaved by 5 ... More
Development of a SYBR safe technique for the sensitive detection of DNA in cesium chloride density gradients for stable isotope probing assays.
Authors:Martineau C, Whyte LG, Greer CW,
Journal:J Microbiol Methods
PubMed ID:18329741
SYBR safe, a fluorescent nucleic acid stain, was evaluated as a replacement for ethidium bromide (EtBr) in cesium chloride (CsCl) density gradients for DNA stable isotope probing (DNA-SIP) assays. The separation of 12C- and 13C-labelled DNA using SYBR safe gave similar results to those obtained using EtBr with pure cultures ... More
Single step protocol to purify recombinant proteins with low endotoxin contents.
Authors:Reichelt P, Schwarz C, Donzeau M
Journal:Protein Expr Purif
PubMed ID:16290005
Endotoxin is an unwanted by product of recombinant proteins purified from Escherichia coli. The inherent toxicity of endotoxins makes their removal an important step for the proteins' application in several biological assays and for safe parenteral administration. The method described in this paper is a one-step protocol which is effective ... More
5-Methyltetrahydrofolate inhibits photosensitization reactions and strand breaks in DNA.
Authors:Offer T, Ames BN, Bailey SW, Sabens EA, Nozawa M, Ayling JE
Journal:FASEB J
PubMed ID:17341682
The known functions of folate are to support one-carbon metabolism and to serve as photoreceptors for cryptochromes and photolyases. We demonstrate that 5-methyltetrahydrofolate (5-MTHF, the predominant folate in plasma) is also a potent, near diffusion limited, scavenger of singlet oxygen and quencher of excited photosensitizers. Both pathways result in decomposition ... More