The supplier advises that they have not yet validated any lysis buffers for use with cell samples in conjunction with this kit. Additionally, they recommend using an untreated, clear, flat-bottom plate for colorimetric measurements. Therefore, it would be preferable to transfer the samples to such a plate for running the assay.
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Wybierz wielkość
| Do Państwa/SKU | Dostępność | Cena netto |
|---|---|---|
1 kit | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 2160,00 zł |
Informacje o tej pozycji
2160,00 zł
detection method
colorimetric
relevant disease(s)
endocrinological disorders, diabetes; gastrointestinal diseases
storage temp.
−20°C
General description
Application
Biochem/physiol Actions
Features and Benefits
Disclaimer
1 of 1
Ta pozycja | ||
|---|---|---|
| description sufficient for 100 colorimetric tests | description sufficient for 180 colorimetric tests | description Sufficient for 100 colorimetric tests |
| detection method colorimetric | detection method colorimetric | detection method colorimetric |
| storage temp. −20°C | storage temp. 2-8°C | storage temp. −20°C |
| relevant disease(s) endocrinological disorders, diabetes; gastrointestinal diseases | relevant disease(s) hematological disorder; gastrointestinal diseases | relevant disease(s) diabetes |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Klasa składowania
3 - Flammable liquids
flash_point_f
75.2 °F - closed cup
flash_point_c
24 °C - closed cup
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What are the recommended methods for homogenizing or lysing cells in a 96-well plate for the MAK317 Sorbitol Dehydrogenase assay kit? The manual advises against using proteolytic enzymes and suggests using a rubber policeman, which is not suitable for a 96-well plate. Are there any recommendations for a mild lysing buffer with minimal impact on the assay outcome? Additionally, is it possible and recommended to run the assay in the same 96-well plate, or is transferring the samples to a new plate necessary?
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