Endogenous Biotin-Blocking Kit
Endogenous Biotin-Blocking Kit
Invitrogen™

Endogenous Biotin-Blocking Kit

The Endogenous Biotin-Blocking Kit provides a method and reagents for a pretreatment that reduces or eliminates background signals when biotin-avidinRead more
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Catalog NumberQuantity
E213901 kit
Catalog number E21390
Price (CNY)
3,839.00
Each
Add to cart
Quantity:
1 kit
Price (CNY)
3,839.00
Each
Add to cart
The Endogenous Biotin-Blocking Kit provides a method and reagents for a pretreatment that reduces or eliminates background signals when biotin-avidin or biotin-streptavidin detection systems are used to identify cellular targets.

The Endogenous Biotin-Blocking Kit offers:
• Improved results—increased signal-to-noise ratio facilitates cell target identification
• Ease of use—pipette-free dropper bottle offers speed and convenience
• Fast—endogenous background reduction in under an hour
• Flexibility—the kit can be used to help improve results from conventional immunohistochemistry, immunocytochemistry, RNA FISH, and ELISA procedures

Biotin occurs naturally, functioning as an enzyme cofactor in the cytosol and mitochondria of a wide variety of cell types. The Endogenous Biotin-Blocking Kit minimizes interference from the endogenous biotin found in enzymes of mammalian cells and tissues, through a two-step blocking strategy. First, an excess of unlabeled streptavidin is added to the specimen to bind endogenous biotin-rich enzymes. The streptavidin is subsequently blocked with an excess of unlabeled biotin, effectively rendering the cell or tissue sample free of available biotin-binding sites.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Quantity1 kit
Reagent TypeBlocking⁄Background Suppression Reagent
Shipping ConditionRoom Temperature
TypeEndogenous Biotin-Blocking Kit
Unit SizeEach
Contents & Storage
Store in refrigerator at 2°C to 8°C

Citations & References (4)

Citations & References
Abstract
A facile method for immunofluorescence microscopy of highly autofluorescent human retinal sections using nanoparticles with large Stokes shifts.
Authors:Petty HR, Elner VM, Kawaji T, Clark A, Thompson D, Yang DL,
Journal:J Neurosci Methods
PubMed ID:20619292
'The human retina is rich in autofluorescent species, such as lipofuscin and melanin. Consequently, it is difficult to localize antigens in the human retina using immunofluorescence microscopy. To address this issue, we have developed a methodology to tag retinal antigens using quantum dot nanoparticles that absorb in the ultraviolet and ... More
Prevention of nonspecific binding of avidin.
Authors:Duhamel RC, Whitehead JS
Journal:Methods Enzymol
PubMed ID:2388571
Suppression of endogenous avidin-binding activity in tissues and its relevance to biotin-avidin detection systems.
Authors:Wood GS, Warnke R
Journal:J Histochem Cytochem
PubMed ID:7028859
As biotin-avidin systems continue to be developed for applications involving single cells, cell suspensions, and especially tissue sections, the need arises for a method of blocking endogenous avidin-binding activity. One such method is described and its proposed mechanism is discussed. Utilizing this method, endogenous avidin-binding activity was detected and suppressed ... More
Simultaneous inhibition of endogenous avidin-binding activity and peroxidase applicable for the avidin-biotin system using monoclonal antibodies.
Authors:Matsumoto Y
Journal:Histochemistry
PubMed ID:2415495
The use of the avidin-biotin technique in immunoperoxidase staining provides a simple and highly sensitive method for detecting the localization of antigens defined by monoclonal antibodies. However, endogenous biotin, which is widely distributed in tissues, often causes non-specific staining by binding to avidin [endogenous avidin-binding activity (EABA)]. Endogenous peroxidase activity ... More