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For USA call : (800) 631-9384
Immunoasaay Enhancers
for Researchers and Manufacturers
READY TO USE TMB FOR HISTOCHEMISTRY &
HYBRIDIZATION APPLICATIONS
-see also TMB-PPT for use with aqueous based reagents and for blotting use
catalog#RDI-TMBSH-1L € 350.00/500ml €
538.00/1
Liter € 475.00/Liter 5-9
USE: For the Immunohistochemical
Localization of Peroxidase Labeled Probes May also be Employed for in situ
Hybridization and Blotting Procedures Stable up to 18 months at room temp or 24
months at 4 DEG C.
Background: Tetramethylbenzidine (TMB) {3,3',5,5'Tetramethylbenzidine} is an
excellent substrate for detecting horseradish peroxidase (HRP) labeled probes.
TMB reagents for ELISA and blotting techniques have been available for several
years. Histochemically, TMB has been utilized primarily for the study of
retrograde axonal transport. To prevent needle formation during color
development, sodium nitroprusside in combination with a low pH was used. Recent
publications have described stabilization of the TMB precipitate with ammonium
hexamolybdate or sodium tungstate. Methyl salicylate has also been employed to
render the TMB reaction product insoluble in alcohols.
This new RDI product is a NEW, stable-single component TMB for histochemical use
containing none of these stabilizers and enhancers. The final reaction product
is not affected by ethanol, xylene or xylene substitutes. Thus dehydration
through alcohols to xylene and mounting the sections in a xylene type medium is
possible. The product may also be used for blotting procedures.
Method: After reacting with a HRP labeled
probe, tissue sections or blots are incubated in the TMB solution. A one
electron oxidation occurs resulting in the formation of a stable blue
precipitate at the sites of HRP activity.
REAGENTS PROVIDED
Tetramethylbenzidine Solution: Contains TMB, 1.25 mMol L(-1) in
an acetate buffer, pH 4.9. Also contains proprietary stabilizers and
precipitating agents.
Store at room temperature or store at 4-8 DEG C, bring to room temp before use.
Discard if solution is turbid or blue
Avoid exposure to direct sunlight, iron and copper salts and
bleach
Neutral Red Solution:(not included, available spearately)
Contains Neutral Red, 0.025% buffered at pH 5.1 Store at room temperature
Discard if a precipitate forms
SAMPLE PROCEDURE: (must be optimized
for each application):
1. Add primary antibody and incubate sections (blots for an ap propriate
interval.
2. Wash sections in a buffer such as PBS containing 0.05% Tween 20.
3. Block endogenous peroxidase, if necessary, by incubating sections in absolute
methanol at room temperature.
4. Wash briefly in PBS.
5. Incubate sections for 30 minutes at room temperature in PBS containing 0.03%
hydrogen peroxide.
6. Wash sections in PBS-Tween-20.
7. Add peroxidase labeled probe and incubate for an appropriate interval
NOTE: The HRP probe must be titered.
For example, a 1:50 dilution of an HRP conjugate that performs well for DAB must
be diluted 1:800 for use with TMB.
8. Wash sections in PBS-Tween-20.
9. Cover sections with TMB solution and incubate 5-15 minutes.
10. After TMB incubation is complete, stop reaction by incubating 10 minutes in
deionized water.
11. Counterstain 30-60 seconds in Neutral Red Solution.
12. Rinse in deionized water the dehydrate rapidly through alcohols to xylene.
13. Mount sections using a xylene based medium.
RESULTS
Site of HRP activity will be brilliant blue.
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