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20X LumiGLO® Reagent and 20X Peroxide #7003

Item# Description List Price Web Price Qty
7003P 20X LumiGLO® Reagent and 20X Peroxide - 5 ml each $90.00
$81.00
$54.00
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7003S 20X LumiGLO® Reagent and 20X Peroxide - 25 ml each $287.00
$258.30
$172.20
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*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca
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Description

LumiGLO®* chemiluminescent substrate is a luminol-based system designed for use with our Phototope®-HRP detection assays utilizing peroxidase-labeled antibodies immobilized on membranes. In the presence of hydrogen peroxide, horseradish peroxidase (HRP) converts luminol to an excited intermediate dianion. This dianion emits light on return to its ground state. Light emission is maximal immediately after exposure of the substrate to HRP and continues for 0.5-1 hour. Light can be captured on X-ray film, typically by exposure for a few seconds. Maximum sensitivity can be obtained by longer exposure. *Avoid repeated exposure to skin (see enclosed Material Safety Data Sheet or refer to our website for further information).

Western Blotting

Western Blotting

After the primary antibody is bound to the target protein, a complex with HRP-linked secondary antibody is formed. The LumiGLO® is added and emits light during enzyme catalyzed decomposition.

Directions for Use

(a) Wash membrane-bound HRP (antibody conjugate) three times, for 5 minutes in TBS/T.

(b) Prepare substrate by diluting 20X LumiGLO® and 20X Peroxide to 1X in water (e.g. for 10 ml, add 0.5 ml LumiGLO® and 0.5 ml peroxide to 9.0 ml water).

(c) Incubate substrate with membrane for 1 minute, remove excess solution (membrane remains wet), wrap in plastic and expose to X-ray film. 

Solutions and Reagents

Prepare solutions with Milli-Q® or equivalently purified water.

Wash Buffer (TBS/T): 20 mM Tris-HCl (pH 7.6),

137 mM NaCl and 0.1% Tween-20

Advantages of the Phototope® Western Detection System

-Sensitivity: Detection of sub-picogram amounts of protein is routine with good primary antisera.

-Speed: Less than 1 hour is required for the entire detection procedure. Exposure times are seconds to minutes.

-Multiple Exposures: Light is emitted at a constant rate for several minutes, so you can perform multiple exposures to optimize signal intensity. Re-exposure at a future date is achieved by simply adding more reagent.

Method Overview

There are six basic steps in the Western blotting procedures with the Phototope®-HRP Western Blot Detection System.

  1. Polyacrylamide Gel Electrophoresis of Proteins: Separate the protein samples and molecular weight standards by polyacrylamide gel electrophoresis.
  2. Transfer: Transfer the protein to membrane by standard electroblotting.
  3. Block Membrane: Block to saturate nonspecific binding sites on the membrane.
  4. 1° Antibody: Incubate the membrane with the primary antibody.
  5. 2° Antibody: Incubate the membrane with HRP-linked anti-rabbit IgG and HRP-linked anti-biotin antibodies.
  6. Chemiluminescent Detection: Add LumiGLO® reagent and capture the emitted light on X-ray film.

Background

Chemiluminescence systems have emerged as the best all-around method for western blot detection. They eliminate the hazards associated with radioactive materials and toxic chromogenic substrates. The speed and sensitivity of these methods are unequalled by traditional alternatives, and because results are generated on film, it is possible to record and store data permanently. Blots detected with chemiluminescent methods are easily stripped for subsequent reprobing with additional antibodies. HRP-conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent substrates to generate the light signal. HRP conjugates have a very high turnover rate, yielding good sensitivity with short reaction times.

Application References

  • Maude, S.L. et al. (2012) Blood 120, 3510-8. Applications: Western Blotting.

Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know!


 

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