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® Chromogenic Kits detect proteins that have been immobilized on membranes (nitrocellulose or PVDF) following western transfer or bound directlyRead more
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Catalog NumberQuantity
WB71051 kit
Catalog number WB7105
Price (CNY)
6,764.00
1 kit
Add to cart
Quantity:
1 kit
Price (CNY)
6,764.00
1 kit
Add to cart
WesternBreeze® Chromogenic Kits detect proteins that have been immobilized on membranes (nitrocellulose or PVDF) following western transfer or bound directly from solution (dot blots). Detection is accomplished with a ready-to-use BCIP/NBT substrate for alkaline phosphatase. Non-fading purple precipitates develop at the protein bands on the membrane. WesternBreeze® chromogenic offers:

• Clear background
• High sensitivity-low picogram levels detectable
• High specificity
• One simple protocol-no optimization required
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cross ReactivityRabbit
Quantity1 kit
ReactivityRabbit
Shipping ConditionWet Ice
Substrate TypeAP (Alkaline Phosphatase) Substrate
Detection MethodChromogenic
Membrane CompatibilityNitrocellulose, PVDF
Product LineWesternBreeze
Product TypeWestern Blot Kit
Unit Size1 kit
Contents & Storage
The WesternBreeze Chromogenic kits include blocking solutions, primary antibody diluent, ready-to-use secondary antibody solution (anti-mouse, anti-rabbit or anti-goat), ready-to-use chromogenic substrate, wash solutions, and incubation trays. Each kit contains complete reagents for 20 mini-blots.

Store the kits at 2–8°C. Guaranteed stable for 6 months when properly stored.

Frequently asked questions (FAQs)

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.

Citations & References (2)

Citations & References
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