Colloidal Blue Staining Kit
Colloidal Blue Staining Kit
Invitrogen™

Colloidal Blue Staining Kit

Das Colloidal Blue Färbekit ermöglicht es, mit minimalem Aufwand Proteinmengen in 1D- oder 2D-PAGE Gelen im Nanogramm-Bereich nachzuweisen, und benötigtWeitere Informationen
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KatalognummerMenge
LC60251 Kit
Katalognummer LC6025
Preis (EUR)
356,00
Each
Zum Warenkorb hinzufügen
Menge:
1 Kit
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
356,00
Each
Zum Warenkorb hinzufügen
Das Colloidal Blue Färbekit ermöglicht es, mit minimalem Aufwand Proteinmengen in 1D- oder 2D-PAGE Gelen im Nanogramm-Bereich nachzuweisen, und benötigt für die Entfärbung lediglich Wasser. Die kolloidchemischen Eigenschaften von Colloidal Blue bewirken, dass freier Farbstoff in der Lösung reduziert und das Protein-Farbstoff-Bindungsverhältnis verbessert wird. Proben werden intensiv gefärbt, und Ergebnisse sind innerhalb von 3 Stunden sichtbar. Durch das Entfärben mit Wasser über Nacht wird eine Hintergrundfärbung eliminiert. Nur eine einfache Lösung muss für das Kit vorbereitet werden. Methanol wird im Färbeschritt benötigt, ist aber nicht im Kit enthalten.

Vergleichen Sie alle Coomassie-Färbemittel ›
Nur für Forschungszwecke. Darf nicht für diagnostische Verfahren eingesetzt werden.
Specifications
DetektionsstelleIn-Gel-Detektion
NachweisverfahrenKolorimetrisch
Menge1 Kit
Haltbarkeit6 Monate
VersandbedingungRaumtemperatur
ZielmolekülProtein
Marker oder FarbstoffCoomassie
ProdukttypProtein-Gel-Färbekit
Unit SizeEach
Inhalt und Lagerung
Das Colloidal Blue Färbekit wird mit ausreichend Färbung A und Färbung B geliefert, um 25 Mini-Gele zu färben Das Kit bei Raumtemperatur lagern . Das Kit wird bei ordnungsgemäßer Lagerung 6 Monate lang garantiert, sofern in der Produktdokumentation nicht anders angegeben.

Häufig gestellte Fragen (FAQ)

Can I use the Colloidal Blue Staining Kit (Cat. No. LC6025) for membrane staining to detect proteins that are transferred to a membrane?

It is not recommended because the background will be too high. Better alternatives include: 1) Invitrogen Reversible Membrane Protein Stain Kit (Cat. No. IB7710).

2) Coomassie (non-colloidal) staining: stain in 0.1% Coomassie Blue R-250 in 50% methanol for 5 min and destain with several changes of 50% methanol and 10% acetic acid. Rinse with several changes of water, air dry and store for up to 12 months at -20°C. Sensitivity is approximately at the 50-100 ng level.

3) Use SimplyBlue SafeStain (Cat. No. LC6060). The SimplyBlue SafeStain manual has the protocol for staining PVDF membranes, but it is not recommended for nitrocellulose because of high background.

4) Amido Black: same as Coomassie but less sensitive.

5) Ponceau S: same as Coomassie but less sensitive.

6) UV transillumination: place membrane on filter paper after blot is finished and allow to dry at room temperature for about 10 min. Rewet in 20% methanol and view the blot in front of white light while it is still wet; the bands will look more translucent than the membrane. If the bands disappear as the membranes dries, rewet again.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

Why is Coomassie G-250 used as the tracking dye in NuPAGE LDS Sample Buffer instead of bromophenol blue?

Coomassie G-250 will give a sharp dye front with both NuPAGE MES and MOPS Running Buffers and is therefore used as the tracking dye in the NuPAGE LDS Sample Buffer.

Bromophenol blue runs more slowly than some peptides with the NuPAGE MES Running Buffer system.

Coomassie G-250 migrates much closer to the moving ion front than bromophenol blue, ensuring that small peptides will not be run too far (e.g., off the gel).

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

Is the SimplyBlue SafeStain the appropriate stain for quantitation by densitometry?

The Colloidal Blue Staining Kit (Cat. No. LC6025) is best for quantitation by densitometry. You can also use SimplyBlue SafeStain for this application.

The great advantage of SimplyBlue SafeStain is that it is very easy to use and safe.

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

The sensitivity of my SimplyBlue SafeStain seems to be decreasing over time. Why is this?

Check the cap on the bottle. If the bottles are not tightly sealed, the alcohol can evaporate from the stain causing substantial decrease in stain sensitivity.

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

How do I destain proteins on a PVDF membrane that were stained with SimplyBlue SafeStain?

After staining with SimplyBlue SafeStain, use deionized water for the less strongly retained protein bands on the PVDF membrane.

Increasing methanol or ethanol concentrations up to 70% should destain any remaining bands. You can leave the membrane in the destain indefinitely.

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

Zitierungen und Referenzen (4)

Zitierungen und Referenzen
Abstract
SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcription.
Authors: Sterner David E; Belotserkovskaya Rimma; Berger Shelley L;
Journal:Proc Natl Acad Sci U S A
PubMed ID:12186975
'Spt-Ada-Gcn5 acetyltransferase (SAGA) is a previously described histone acetyltransferase/transcriptional coactivator complex in yeast. At promoters of certain genes (HIS3 and TRP3), SAGA has an inhibitory function involving a nonproductive TATA-binding protein interaction mediated by the Spt3 and Spt8 subunits. Related to this, Spt8-less SAGA is a major form of the ... More
Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex.
Authors:Tong JK, Hassig CA, Schnitzler GR, Kingston RE, Schreiber SL
Journal:Nature
PubMed ID:9804427
'The dynamic assembly and remodelling of eukaryotic chromosomes facilitate fundamental cellular processes such as DNA replication and gene transcription. The repeating unit of eukaryotic chromosomes is the nucleosome core, consisting of DNA wound about a defined octamer of histone proteins. Two enzymatic processes that regulate transcription by targeting elements of ... More
A family of chromatin remodeling factors related to Williams syndrome transcription factor
Authors:Bochar DA, Savard J, Wang W, Lafleur DW, Moore P, Cote J, Shiekhattar R
Journal:Proc Natl Acad Sci U S A
PubMed ID:10655480
Chromatin remodeling complexes have been implicated in the disruption or reformation of nucleosomal arrays resulting in modulation of transcription, DNA replication, and DNA repair. Here we report the isolation of WCRF, a new chromatin-remodeling complex from HeLa cells. WCRF is composed of two subunits, WCRF135, the human homolog of Drosophila ... More
A method to identify serine kinase substrates. Akt phosphorylates a novel adipocyte protein with a Rab GTPase-activating protein (GAP) domain.
Authors: Kane Susan; Sano Hiroyuki; Liu Simon C H; Asara John M; Lane William S; Garner Charles C; Lienhard Gustav E;
Journal:J Biol Chem
PubMed ID:11994271
This study describes a method for the identification of the substrates of specific serine kinases. An antibody specific for the phosphomotif generated by the kinase is used to isolate phosphorylated substrates by immunoprecipitation, and the isolated proteins are identified by tandem mass spectrometry of peptides. This method was applied to ... More