Vybrat velikost
3 570,00 Kč
5 910,00 Kč
3 570,00 Kč
Očekávané datum odeslání22. prosince 2025podrobné informace
O této položce
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Název produktu
TMB/E Ultra Sensitive, Blue, Horseradish Peroxidase Substrate (soluble), 100 ml TMB/E Ultra Sensitive, Blue, Horseradish Peroxidase Substrate (soluble) for ELISA & Immunohistochemistry.
form
liquid
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable
immunohistochemistry: suitable
λmax
450 nm
shipped in
wet ice
Quality Level
1 of 4
Tato položka | ES001 | T9455 | T5569 |
|---|---|---|---|
| technique(s) ELISA: suitable, immunohistochemistry: suitable | technique(s) ELISA: suitable | technique(s) - | technique(s) - |
| Quality Level 100 | Quality Level - | Quality Level 200 | Quality Level - |
| form liquid | form liquid | form solution | form liquid |
| shipped in wet ice | shipped in wet ice | shipped in - | shipped in wet ice |
| manufacturer/tradename Chemicon® | manufacturer/tradename Chemicon® | manufacturer/tradename - | manufacturer/tradename - |
| λmax 450 nm | λmax 450 nm | λmax - | λmax - |
Application
After completion of analyte binding to a solid phase and reaction with a HRP labeled probe, ES022 is added. Oxidation of TMB produces a blue reaction product that is measured at 650 nm. The color formation as a function of time can be recorded or the reaction stopped with sodium fluoride after a fixed interval. Increased sensitivity can be achieved by converting the blue radical to the diimine by addition of acid. The resulting yellow color is measured immediately at 450 nm.
SAMPLE PROCEDURE:
1. Complete all required incubations with antibodies, probes, HRP labeled reagents.
2. Wash plate at least 4 times with PBS or Tris buffered saline containing 0.1% Tween-20.
3. After the final wash, shake and blot all residual buffer from plate wells.
4. Add 0.1 mL of ES022 (TMBE Solution) to appropriate wells and incubate 5-30 minutes.
Note: The reaction time will depend upon the activity of the HRP probe. If color develops too briskly, zero order kinetics will not prevail. Dilution of the probe, antibody or HRP labeled reagent may be required.
5. The reaction can be monitored as a function of time for kinetic assays or stopped with 0.1 mL of 0.3 Mol/L of sulphuric acid or 0.1% sodium fluoride and read at 450 nm.
6. If the procedure demands conversion to the yellow diimine, add 0.1 mL of either acid described in the reagent section above and record the absorbance within 5 minutes.
Variations of time, reagent volume and temperature require standardization by the user.
Disclaimer
General description
Physical form
Liquid solution containing TMB, 2.08 μMol L(-1) and Hydrogen Peroxide, citric acid buffer at pH 3.3. Also contains non-toxic proprietary stabilizers.
MATERIALS REQUIRED: Reagents Required for Stopping the Reaction, But Not Provided
A. 0.3 Mol L sulphuric acid for stopping the reaction and preserving blue chromogen.
Note: Reagent grade water must contain less than 10(-7) Mol/L of iron or copper salts otherwise unreacted TMB will be converted non-enzymatically to the diimine.
Preparation Note
Warm to room temperature prior to use.
REAGENT PROVIDED: Liquid solution containing TMB, 2.08 mMol L(-1) and Hydrogen Peroxide, citric acid buffer at pH 3.3. Also contains non-toxic proprietary stabilizers.
Legal Information
Skladovací třída
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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