WesternBreeze™ Chromogenic Kit, anti-rabbit
WesternBreeze™ Chromogenic Kit, anti-rabbit
WesternBreeze™ Chromogenic Kit, anti-rabbit
WesternBreeze™ Chromogenic Kit, anti-rabbit
WesternBreeze™ Chromogenic Kit, anti-rabbit
Invitrogen™

WesternBreeze™ Chromogenic Kit, anti-rabbit

WesternBreeze® Chromogen-Kits dienen zum Nachweis von Proteinen, die auf Membranen (Nitrozellulose oder PVDF) nach dem Western-Transfer immobilisiert oder direkt ausWeitere Informationen
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KatalognummerMenge
WB71051 Kit
Katalognummer WB7105
Preis (EUR)
504,00
1 kit
Zum Warenkorb hinzufügen
Menge:
1 Kit
Preis (EUR)
504,00
1 kit
Zum Warenkorb hinzufügen
WesternBreeze® Chromogen-Kits dienen zum Nachweis von Proteinen, die auf Membranen (Nitrozellulose oder PVDF) nach dem Western-Transfer immobilisiert oder direkt aus der Lösung gebunden wurden (Dot-Blots). Der Nachweis erfolgt mit einem gebrauchsfertigen BCIP/NBT-Substrat für alkalische Phosphatase. An den Proteinbändern an der Membran entwickeln sich nicht verblassende violette Präzipitate. WesternBreeze® Chromogen bietet:

• Klarer Hintergrund
• Hohe Empfindlichkeit – niedrige Picogrammwerte nachweisbar
• Hohe Spezifität
• Ein einfaches Protokoll – keine Optimierung erforderlich
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
KreuzreaktivitätKaninchen
Menge1 Kit
ReaktivitätKaninchen
VersandbedingungNasseis
SubstrattypAP-Substrat (alkalische Phosphatase)
NachweisverfahrenChromogen
Membrane CompatibilityNitrozellulose, PVDF
ProduktlinieWesternBreeze
ProdukttypWestern-Blot-Kit
Unit Size1 kit
Inhalt und Lagerung
Die WesternBreeze™ Chromogen-Kits enthalten Blockierungslösungen, Verdünnungsmittel für primäre Antikörper, gebrauchsfertige sekundäre Antikörperlösung (Anti-Maus, Anti-Kaninchen oder Anti-Ziege), gebrauchsfertiges chromogenes Substrat, Waschlösungen und Inkubationstabletts. Jedes Kit enthält genügend Reagenzien für 20 Mini-Blots. Lagern Sie die Kits bei +4 °C. Bei ordnungsgemäßer Lagerung garantiert 6 Monate stabil.

Häufig gestellte Fragen (FAQ)

Why is the actual band size on a western blot different from the predicted size of the protein?

Western blotting is based on the separation of proteins by their size on a gel. However, migration of proteins through the gel matrix is also affected by other factors, which may cause the observed band size to be different from the predicted size.

Common causes are:
-Post-translational modification; for example phosphorylation and glycosylation increase the size of the protein
-Post-translation cleavage; many proteins are synthesized as precursor proteins, and then cleaved to give the active form
-Multimers, for example dimerization of a protein. This is usually prevented under reducing conditions, although strong interactions can result in the appearance of higher bands
-Splice variants; alternative splicing may result in different sized proteins being produced from the same gene
-Relative charge; the composition of amino acids (charged vs. non-charged)

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

What are the standard lysis buffers used with mammalian cells for detection of protein expression by immunoprecipitation (IP) or Western blot analysis?

The most commonly used buffer is RIPA Buffer with SDS. We offer RIPA Buffer (Cat. Nos. 89900 and 89901). We also offer the Pierce IP Lysis buffer (Cat. Nos. 87787 and 87788) as well as M-PER (Cat. Nos. 78501, 78503, and 78505).

Find additional tips, troubleshooting help, and resources within our Cell Lysis and Fractionation Support Center.

What conditions do you recommend for overnight Western transfer?

Doing an overnight Westerm transfer is not the preferred method but can be done. The power should be lowered and the buffer should be chilled or the unit should be placed in the cold room to prevent overheating. You may try an overnight transfer at 5-15 V and adjust accordingly. You may also wish to put a second membrane behind the first in order to bind any proteins that transfer through the first membrane. You can use both membranes for staining, immunoblotting, or analysis.

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

Can I purchase the Secondary Antibody solutions from the WesternBreeze Chromogenic Detection kits as standalone products?

The goat anti-mouse and goat anti-rabbit secondary antibody solutions AP-conjugated are available as standalone products (Cat. Nos. WP20006 and WP20007) but the rabbit anti-goat secondary antibody solution AP-conjugated is not available as a standalone product.

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

Can I purchase the Blocker/Diluent and Antibody Wash solutions from the WesternBreeze Chromogenic Detection kits as standalone products?

Yes, you may purchase them as standalone products using the Cat. Nos. listed below:

- Cat. No. WB7003 (Antibody Wash)
- Cat. No. WB7001 (Blocker/Diluent A)
- Cat. No. WB7002 (Blocker/Diluent B)
- Cat. No. WB7050 (Combo pack containing Blocker/Diluents A & B)

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

Zitierungen und Referenzen (2)

Zitierungen und Referenzen
Abstract
Hop Is an Unusual Homeobox Gene that Modulates Cardiac Development.
Authors: Chen Fabian; Kook Hyun; Milewski Rita; Gitler Aaron; Lu Min; Li Jun; Nazarian Ronniel; Schnepp Robert; Jen Kuangyu; Biben Christine; Runke Greg; Mackay Joel; Novotny Jiri; Schwartz Robert; Harvey Richard; Mullins Mary; Epstein Jonathan;
Journal:Cell
PubMed ID:12297045
'Hop is a small, divergent homeodomain protein that lacks certain conserved residues required for DNA binding. Hop gene expression initiates early in cardiogenesis and continues in cardiomyocytes throughout embryonic and postnatal development. Genetic and biochemical data indicate that Hop functions directly downstream of Nkx2-5. Inactivation of Hop in mice by ... More
An iron-regulated ferric reductase associated with the absorption of dietary iron.
Authors:McKie AT, Barrow D, Latunde-Dada GO, Rolfs A, Sager G, Mudaly E, Mudaly M, Richardson C, Barlow D, Bomford A, Peters TJ, Raja KB, Shirali S, Hediger MA, Farzaneh F, Simpson RJ.
Journal:Science
PubMed ID:11230685
The ability of intestinal mucosa to absorb dietary ferric iron is attributed to the presence of a brush-border membrane reductase activity that displays adaptive responses to iron status. We have isolated a complementary DNA, Dcytb (for duodenal cytochrome b), which encoded a putative plasma membrane di-heme protein in mouse duodenal ... More