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WBAVDFL01

Millipore

Immobilon® Block - FL (Fluorescent Blocker)

Fluorescent Detection for Western blotting, dot/slot blotting, mass spectrometry and fluorescence assays

Synonym(s):

Fluorescent Blocker, Immobilon Blocking Reagent

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About This Item

UNSPSC Code:
41116010
eCl@ss:
42029053
NACRES:
NB.22

Quality Level

packaging

pkg of 500 mL

manufacturer/tradename

Immobilon®

technique(s)

western blot: suitable

membrane area

1000 cm2 , membrane coverage

detection method

fluorometric

shipped in

ambient

storage temp.

15-25°C

General description

Immobilon® Block Noise Cancelling Reagents are designed especially for Western blotting applications. This family of protein-free, ready-to-use buffers has been optimized to reduce background levels when using chemiluminescence, fluorescent, or phosphotyrosine detection. Bløk buffers are ideal for use with Immobilon-P Western blotting membranes and the SNAP i.d. system, and are also compatible with standard Western blotting techniques.

application

For use on immunoblots.

Packaging

Sufficient reagent for 19 mini blots (8x7 cm)

Quality

For optimum results, use Immobilon-P membrane for chemiluminescence (luminol) or visual detection (e.g. TMB), and Immobilon-FL membrane for fluorescent detection applications.

Storage and Stability

Stable for 2 years at 20–25°C

Legal Information

Immobilon is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yann Ehinger et al.
EMBO molecular medicine, 12(2), e10889-e10889 (2020-01-09)
Mutations in the X-linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder for which there is no treatment. Several studies have linked the loss of MeCP2 function to alterations of brain-derived neurotrophic factor (BDNF) levels, but

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