NuPAGE LDS-Probenpuffer (4X) dient zur Vorbereitung von Proteinproben für die denaturierende Gelelektrophorese mit Bis-Tris- oder Tris-Acetat-Gelen. Enthält Lithiumdodecylsulfat bei einemWeitere Informationen
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Katalognummer
Menge
NP0007
10 ml
NP0008
250 ml
2 Optionen
Katalognummer NP0007
Preis (EUR)
27,65
Exklusiv online
28,71
Ersparnis 1,06 (4%)
Each
Zum Warenkorb hinzufügen
Menge:
10 ml
Preis (EUR)
27,65
Exklusiv online
28,71
Ersparnis 1,06 (4%)
Each
Zum Warenkorb hinzufügen
NuPAGE LDS-Probenpuffer (4X) dient zur Vorbereitung von Proteinproben für die denaturierende Gelelektrophorese mit Bis-Tris- oder Tris-Acetat-Gelen. Enthält Lithiumdodecylsulfat bei einem pH-Wert von 8,4, was eine maximale Aktivität des Reduktionsmittels ermöglicht.
NuPAGE LDS-Probenpuffer enthält Coomassie G250 und Phenolrot als Tracking-Farbstoffe anstelle von Bromphenolblau. Coomassie G250 bietet eine scharfe Farbstofffront mit MES- und MOPS SDS-Laufpuffern und wandert viel näher an die bewegliche Ionenfront als Bromphenolblau. Bromphenolblau läuft langsamer als einige Peptide mit MES SDS-Laufpuffer. Dadurch wird sichergestellt, dass kleine Peptide nicht von den Gelen ablaufen.
Anwendung: Die Probe in einer 1X-Verdünnung (reduziert oder nicht reduziert) 10 Minuten lang bei 70 °C erhitzen, um optimale Ergebnisse zu erzielen.
Hinweis: NuPAGE LDS-Probenpuffer muss vor Gebrauch auf Raumtemperatur (25 °C) gebracht werden. Es handelt sich um eine hochviskose und konzentrierte Lösung, die im Vergleich zur SDS-Menge in typischen Probenpuffern doppelt so viel LDS enthält. NuPAGE LDS Probenpuffer enthält auch Glycerin in höherer Konzentration.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
PufferProbenladepuffer
Konzentration4 X
GelkompatibilitätNuPAGE™ Gele
Menge10 ml
VersandbedingungZugelassen für den Versand bei Raumtemperatur oder auf nassem Eis
GeltypNuPAGE Gel
ProduktlinieNuPAGE
ProdukttypLDS-Probenpuffer
Unit SizeEach
Inhalt und Lagerung
Probenpuffer (4X) mit Lithiumdodecylsulfat (LDS) bei pH 8,5 mit SERVA Blue G250 und Phenolrot.
Bei 4 bis 25 °C lagern.
Häufig gestellte Fragen (FAQ)
Can I prepare my protein sample with the reducing agent and store it for future use?
DTT is not stable, so it must be added and the reduction performed just prior to loading your samples.
My LDS or SDS sample buffer precipitates when stored at 4 degrees C. Can I warm it up? Can I store it at room temperature?
Precipitation of the LDS or SDS at 4 degrees C is normal. Bring the buffer to room temperature and mix until the LDS/SDS goes into solution. If you do not want to wait for it to dissolve, you can store the sample buffer at room temperature.
While they are both Bis-Tris based gels, the chemistries are very different since Bolt gels are optimized for western blotting. Another key difference is the wedge well design of the Bolt gels, which allows larger sample volumes to be loaded.
What is the advantage of NuPAGE Gels over regular Tris-Glycine gels?
The neutral operating pH of the NuPAGE Gels and buffers provides following advantages over the Laemmli system: -Longer shelf life of 8-12 months due to improved gel stability -Improved protein stability during electrophoresis at neutral pH resulting in sharper band resolution and accurate results (Moos et al, 1998) -Complete reduction of disulfides under mild heating conditions (70 degrees C for 10 min) and absence of cleavage of asp-pro bonds using the NuPAGE LDS Sample buffer (pH > 7.0 at 70 degrees C) -Reduced state of the proteins maintained during electrophoresis and blotting of the proteins by the NuPAGE Antioxidant Please refer to the following paper: Moos M Jr, Nguyen NY, Liu TY (1988) Reproducible High Yield Sequencing of Proteins Electrophoretically Separated and Transferred to an Inert Support. J Biol Chem 263:6005-6008.
'The human ov-serpin monocyte neutrophil elastase inhibitor (MNEI) is encoded by a single gene SERPINB1. It is a highly efficient inhibitor of neutrophil granule proteases. Four murine genes with high sequence identity with MNEI were identified and fully sequenced, and these were named EIA, EIB, EIC, and EID. EIA, EIB ... More
Novel Modulation of Neuronal Nicotinic Acetylcholine Receptors by Association with the Endogenous Prototoxin lynx1.
We previously identified lynx1 as a neuronal membrane molecule related to snake alpha-neurotoxins able to modulate nAChRs. Here, we show that lynx1 colocalizes with nAChRs on CNS neurons and physically associates with nAChRs. Single-channel recordings show that lynx1 promotes the largest of three current amplitudes elicited by ACh through alpha(4)beta(2) ... More
Apolipoprotein A-I is a selective target for myeloperoxidase-catalyzed oxidation and functional impairment in subjects with cardiovascular disease.
Authors:Zheng L, Nukuna B, Brennan ML, Sun M, Goormastic M, Settle M, Schmitt D, Fu X, Thomson L, Fox PL, Ischiropoulos H, Smith JD, Kinter M, Hazen SL,
Journal:J Clin Invest
PubMed ID:15314690
In recent studies we demonstrated that systemic levels of protein-bound nitrotyrosine (NO(2)Tyr) and myeloperoxidase (MPO), a protein that catalyzes generation of nitrating oxidants, serve as independent predictors of atherosclerotic risk, burden, and incident cardiac events. We now show both that apolipoprotein A-I (apoA-I), the primary protein constituent of HDL, is ... More
In vivo functional assay of a recombinant aquaporin in Pichia pastoris.
Authors:Daniels MJ, Wood MR, Yeager M,
Journal:Appl Environ Microbiol
PubMed ID:16461705
The water channel protein PvTIP3;1 (alpha-TIP) is a member of the major intrinsic protein (MIP) membrane channel family. We overexpressed this eukaryotic aquaporin in the methylotrophic yeast Pichia pastoris, and immunogold labeling of cellular cryosections showed that the protein accumulated in the plasma membrane, as well as vacuolar and other ... More
Spermidine but not spermine is essential for hypusine biosynthesis and growth in Saccharomyces cerevisiae: Spermine is converted to spermidine in vivo by the FMS1-amine oxidase.
Authors:Chattopadhyay MK, Tabor CW, Tabor H,
Journal:Proc Natl Acad Sci U S A
PubMed ID:14617780
In our earlier work we showed that either spermidine or spermine could support the growth of spe2Delta or spe3Delta polyamine-requiring mutants, but it was unclear whether the cells had a specific requirement for either of these amines. In the current work, we demonstrate that spermidine is specifically required for the ... More