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.
MAK317
Sorbitol Dehydrogenase Assay Kit
sufficient for 100 colorimetric tests
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About This Item
Recommended Products
detection method
colorimetric
relevant disease(s)
endocrinological disorders, diabetes; gastrointestinal diseases
storage temp.
−20°C
Related Categories
General description
Features and Benefits
Suitability
Principle
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
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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