The kit's Technical Bulletin notes that it contains Pyruvate Oxidase, which it utilizes along with Hydrogen Peroxide to create a colored/fluorescent reaction product. Further details characterizing the formulations of the reagents in the kit and the kit's reaction mechanism are proprietary.
Przejdź do
Wybierz wielkość
| Do Państwa/SKU | Dostępność | Cena netto |
|---|---|---|
1 kit | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 2020,00 zł |
Informacje o tej pozycji
2020,00 zł
usage
sufficient for 100 colorimetric or fluorometric tests
input
biological sample(s)
application(s)
pharmaceutical
detection method
colorimetric, fluorometric
relevant disease(s)
gastrointestinal diseases; cancer
storage temp.
−20°C
General description
Application
- Odkrywania leków
- Testowanie żywności i napojów
- Badania chorób neurologicznych
Biochem/physiol Actions
Features and Benefits
Uproszczony proces: Doświadcz usprawnionego procesu z dodatkiem tylko jednego odczynnika roboczego i 30-minutowej reakcji w temperaturze pokojowej, zmniejszając złożoność i oszczędzając cenny czas i wysiłek.
Kompatybilność z systemami o wysokiej wydajności: Łatwe włączenie naszego zestawu do wysokowydajnych systemów obsługi, zapewnia płynne i dokładne przetwarzanie, zwiększając wydajność pracy w laboratorium.
Other Notes
1 of 1
Ta pozycja | |||
|---|---|---|---|
| description sufficient for 100 colorimetric or fluorometric tests | description sufficient for 100 colorimetric or fluorometric tests | description sufficient for 100 colorimetric tests | description sufficient for 100 colorimetric tests |
| detection method colorimetric, fluorometric | detection method colorimetric, fluorometric | detection method colorimetric | detection method colorimetric |
| usage sufficient for 100 colorimetric or fluorometric tests | usage sufficient for 100 colorimetric or fluorometric tests | usage sufficient for 100 colorimetric tests | usage sufficient for 100 colorimetric tests |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
| input biological sample(s) | input culture(s) | input cell | input plasma |
| application(s) pharmaceutical | application(s) - | application(s) - | application(s) cosmetics |
| relevant disease(s) gastrointestinal diseases; cancer | relevant disease(s) cancer | relevant disease(s) endocrinological disorders, diabetes; cancer | relevant disease(s) neurological disorders |
Klasa składowania
10 - Combustible liquids
flash_point_f
188.6 °F
flash_point_c
87 °C
wgk
WGK 2
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Is any of the reagent of this product includes phosphate? I wonder which mechanism or chemical reaction is used for this assay kit (e.g. pyruvate oxidation reaction).
1 answer-
Helpful?
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Could I get a reasonable measurement if I used a 600nm plate reader to measure the output?
1 answer-
A 600 nm excitation wavelength has not been tested for this kit. It is suggested to use 530 nm as the excitation wavelength to achieve reliable results.
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I want to detect E.coli intracellular pyruvate concentration. Therefore, I need to break cells before I detect it. How can I use this kit? I try to use methanol to deal with cells and use freeze-thaw cycle to break. Will methanol have effect to the kit?
1 answer-
This kit has not been tested specifically for use in measuring intracellular pyruvate in E. coli. However, other researchers have used this kit successfully. Methanol is not an interfering substance. Pelleted cells may be quenched and subsequently flash frozen in methanol to lyse. Repeated flash freezing may be applied to assure complete lysis. The combined collected supernatant may then be analyzed by following the recommended protocol. Please see the link below to review.
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/358/918/mak332bul.pdfHelpful?
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Can I use the samples in Lactate Assay buffer (Lactate assay kit sigma MAK064) for this kit or does this buffer interfere with the reaction ?
1 answer-
The assay buffer for Kit MAK064 has not been tested to determine suitability with the Kit MAK332.
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