This product has been discontinued without a replacement. Technical Service has no data describing its use in testing cell lysates.
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detection method
fluorometric
relevant disease(s)
cardiovascular diseases
storage temp.
−20°C
General description
Application
Biochem/physiol Actions
Features and Benefits
Lagerklasse
10 - Combustible liquids
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
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is this product suitable for cell lysate? If possible, i need protocol to prepare sample(cell number, how to lysis etc.)
1 answer-
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Could N-acetyl Cysteine interfere with the MAK255-1KT Cysteine Assay Kit (Fluorometric)? Additionally, would residual H2S also interfere with the assay?
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Since the assay principle is based on the cleavage of the thiol group in reduced Cysteine, N-acetyl Cysteine, which contains the thiol group, is likely to be included in the quantification of cysteine present in the biological fluids by the kit. Additionally, the assay should detect Hydrogen sulfide generated by the enzymatic metabolism of Cysteine. Therefore, sulfide salts (such as Sodium sulfide) as well as residual Hydrogen sulfide in the sample would likely be a significant source of interference.
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Are the standards run in kinetic or endpoint mode? How are they plotted?
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The standards are run in kinetic mode as well. It's important that the delta T (T2-T1) remains consistent for both the standards and the samples, and in all cases, it should fall within the linear range of the plot. For instance, samples could be read from T=2 to T=4 (assuming linearity) and the standards could be read from T=3 to T=5 (again, assuming linearity), ensuring that the delta T remains the same. Subsequently, the delta RFU is plotted for the standards against concentration, and then the samples can be plotted using their delta RFU to determine the concentration.
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Is the product Cysteine Assay Kit (Fluorometric) MAK255 suitable for use with blood plasma?
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The Cysteine Assay Kit (Fluorometric) MAK255 is suitable for use with mammalian plasma samples. Centrifugation of plasma samples is not necessary, as they can be used directly. While the choice of anticoagulant would not make a significant difference, it is generally recommended to avoid EDTA or citrate, which are chelators, and to use heparin instead.
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