SYPRO™ Proteingel-Färbemittel
SYPRO™ Proteingel-Färbemittel
Das tatsächliche Produkt kann abweichen
SYPRO™ Proteingel-Färbemittel
SYPRO™ Proteingel-Färbemittel
SYPRO™ Proteingel-Färbemittel
SYPRO™ Proteingel-Färbemittel
Invitrogen™

SYPRO™ Proteingel-Färbemittel

SYPRO Ruby Protein-Gelfärbung ist eine hochempfindliche, gebrauchsfertige fluoreszierende Färbung für den Nachweis von durch Polyacrylamid-Gelelektrophorese (PAGE) getrennten Gesamtproteinen. Ideal fürWeitere Informationen
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KatalognummerFarbeMenge
S6654
auch als S-6654 bezeichnet
Rot10 x 50 μl
S6650Orange500 μl
S6651Orange10 x 50 μl
S12010Orangefarben500 μl
S6653Rot500 μl
S12001Rubin200 mL
S12000Rubin1 l
S21900Rubin5 l
S12000X3Rubin3 x 1 l
Katalognummer S6654
auch als S-6654 bezeichnet
Preis (EUR)
482,65
キャンペーン価格
508,00
Ersparnis 25,35 (5%)
Each
Zum Warenkorb hinzufügen
Farbe:
Rot
Menge:
10 x 50 μl
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
482,65
キャンペーン価格
508,00
Ersparnis 25,35 (5%)
Each
Zum Warenkorb hinzufügen
SYPRO Ruby Protein-Gelfärbung ist eine hochempfindliche, gebrauchsfertige fluoreszierende Färbung für den Nachweis von durch Polyacrylamid-Gelelektrophorese (PAGE) getrennten Gesamtproteinen. Ideal für den Einsatz in 1D- und 2D-PAGE. Die Empfindlichkeit von SYPRO Ruby Gelfärbung ist mindestens so hoch wie die der besten Silberfärbeverfahren. Gefärbte Proteine können mit einem standardmäßigen UV- oder Blaulicht-Transilluminator oder einem Bildgebungsgerät mit den entsprechenden Filtern oder Lasern betrachtet werden.

Merkmale:
Einfaches Färbeverfahren: kein Entfärben oder zeitgesteuerte Schritte erforderlich
• Linearer Quantifizierungsbereich über drei Größenordnungen
• Kompatibilität mit Massenspektrometrie und Mikrosequenzierung

Vergleich aller Fluoreszenz-Färbemittel ›
Nur für Forschungszwecke. Darf nicht für diagnostische Verfahren eingesetzt werden.
Specifications
Konzentration5000X in DMSO
DetektionsstelleIn-Gel-Detektion
NachweisverfahrenFluoreszenz
Anregung/Emission300, 550/630 nm
Menge10 x 50 μl
VersandbedingungRaumtemperatur
ZielmolekülProtein
FarbeRot
Marker oder FarbstoffSYPRO Rot
ProduktlinieSYPRO
ProdukttypProteingel-Färbemittel
Unit SizeEach
Inhalt und Lagerung
Lagerung bei Raumtemperatur und vor Licht geschützt

Häufig gestellte Fragen (FAQ)

If I increase the final concentration of my SYPRO Orange or SYPRO Red staining solution above 1X, can I increase the signal of my stained proteins?

No. Dye concentrations higher than 1X do not give better detection. Instead, background fluorescence increases and, as the dye concentration increases, the dye becomes self-quenching and the signal actually decreases.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Can I dry my SYPRO Ruby, SYPRO Orange, or SYPRO Red stained gels?

Gels stained with SYPRO dyes can be dried between sheets of cellophane, although there is sometimes a slight decrease in sensitivity. If the gels are dried onto paper, the light will scatter and the sensitivity will decrease. Other plastics are not recommended, as the plastic typically used is not transparent to UV light.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Can I pre-stain proteins with SYPRO Ruby, SYPRO Orange or SYPRO Red Protein Gel Stains and then run them through a gel?

No. Loading solutions contain so much SDS that SYPRO Ruby, SYPRO Orange and SYPRO Red dyes simply localize in the free SDS and bind very little of the proteins. Proteins can be covalently pre-labeled with ATTO-TAG CBQCA (Cat. No. A2333), DDAO succinimidyl ester (Cat. No. C34553) or TAMRA-succinimidyl ester (Cat. No. C2211) dyes, or the TC-FLAsH Expression Analysis Detection Kits (Cat. No. A10067 for orange fluorescence, Cat. No. A10068 for red fluorescence) prior to electrophoresis without affecting protein migration through the gel.

SYPRO Orange or SYPRO Red Protein Gel Stain can be diluted 5000-fold into the cathode (upper) buffer tank to stain proteins during electrophoresis without affecting migration. The problem with doing this is that there is considerable background fluorescence in the gels from the dye interacting with SDS. This can be reduced after electrophoresis by destaining in 7.5% acetic acid for 15-60 minutes. This method also results in poorer protein sensitivity than the standard post-staining method, requires the same amount of time before the gel can be imaged, and contaminates the electrophoresis apparatus.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Zitierungen und Referenzen (60)

Zitierungen und Referenzen
Abstract
Design and characterization of a compact dual channel virus counter.
Authors:Stoffel CL,Kathy RF,Rowlen KL
Journal:Cytometry. Part A : the journal of the International Society for Analytical Cytology
PubMed ID:15830378
Adenosine to inosine editing by ADAR2 requires formation of a ternary complex on the GluR-B R/G site.
Authors:Jaikaran DC, Collins CH, MacMillan AM
Journal:J Biol Chem
PubMed ID:12163487
'RNA editing by members of the ADAR (adenosine deaminase that acts on RNA) enzyme family involves hydrolytic deamination of adenosine to inosine within the context of a double-stranded pre-mRNA substrate. Editing of the human GluR-B transcript is catalyzed by the enzyme ADAR2 at the Q/R and R/G sites. We have ... More
Defining the SNARE complex binding surface of alpha-SNAP: implications for SNARE complex disassembly.
Authors:Marz KE, Lauer JM, Hanson PI
Journal:J Biol Chem
PubMed ID:12730228
'N-Ethylmaleimide-sensitive factor (NSF) and its adaptor protein alpha-soluble NSF attachment protein (alpha-SNAP) sustain membrane trafficking by disassembling soluble NSF attachment protein receptor (SNARE) complexes that form during membrane fusion. To better understand the role of alpha-SNAP in this process, we used site-directed mutagenesis to identify residues in alpha-SNAP that interact ... More
Involvement of DnaE, the second replicative DNA polymerase from Bacillus subtilis, in DNA mutagenesis.
Authors:Le Chatelier E, Bécherel OJ, d'Alençon E, Canceill D, Ehrlich SD, Fuchs RP, Jannière L
Journal:J Biol Chem
PubMed ID:14593098
'In a large group of organisms including low G + C bacteria and eukaryotic cells, DNA synthesis at the replication fork strictly requires two distinct replicative DNA polymerases. These are designated pol C and DnaE in Bacillus subtilis. We recently proposed that DnaE might be preferentially involved in lagging strand ... More
Dynamics of myo1c (myosin-ibeta ) lipid binding and dissociation.
Authors:Tang N, Lin T, Ostap EM
Journal:J Biol Chem
PubMed ID:12221091
'Myosin-I is the single-headed member of the myosin superfamily that associates with lipid membranes. Biochemical experiments have shown that myosin-I membrane binding is the result of electrostatic interactions between the basic tail domain and acidic phospholipids. To better understand the dynamics of myosin-I membrane association, we measured the rates of ... More