This kit has not been tested for use on bacterial cultures and may not be suitable. It would be up to the end user to determine suitability. However, the colorimetric version of this kit, MAK468, has been successfully used in Corynebacterium glutamicum, Klebsiella pneumoniae, Lactobacillus plantarum, Edwardsiella tarda, Acinetobacter baumannii, Auxenochlorella protothecoides, E. coli, and other microbial species. Please see the links below to review this product and protocol.
MAK468 product page:
https://www.sigmaaldrich.com/product/sigma/mak468
MAK468 datasheet:
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/219/480/mak468pis-ms.pdf
MAK460
NAD+/NADH Assay Kit
Sufficient for 100 fluorometric tests
Sinónimos:
NAD/NADH Quantitation Kit
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About This Item
Productos recomendados
Nivel de calidad
aplicaciones
pharmaceutical
método de detección
fluorometric
enfermedades relevantes
cancer, Alzheimer′s disease; neurological disorders, Parkinson′s disease; aging/geriatric diseases
temp. de almacenamiento
−20°C
Descripción general
Aplicación
- Enhanced glycolysis in the myometrium with ectopic endometrium of patients with adenomyosis: a preliminary study.: This study investigates the role of glycolysis in the myometrium of patients with adenomyosis, utilizing the NAD+/NADH Assay Kit to assess metabolic alterations (Huang et al., 2024). 10.1080/09513590.2024.2332411
- Jian-Pi-Yi-Shen formula alleviates renal fibrosis by restoring NAD+ biosynthesis in vivo and in vitro.: This research demonstrates how the Jian-Pi-Yi-Shen formula mitigates renal fibrosis through NAD+ biosynthesis, with the NAD+/NADH Assay Kit playing a crucial role in the biochemical analysis (Gao et al., 2023). 10.18632/aging.205352
- Butyrate inhibits the mitochondrial complex Ι to mediate mitochondria-dependent apoptosis of cervical cancer cells.: The study explores butyrate′s effects on mitochondrial function and apoptosis in cervical cancer cells, employing the NAD+/NADH Assay Kit to measure mitochondrial activity (Zhang et al., 2023). 10.1186/s12906-023-04043-3
- PM2.5 mediates mouse testis Sertoli TM4 cell damage by reducing cellular NAD().: This article investigates the impact of PM2.5 on Sertoli cells in mouse testes, using the NAD+/NADH Assay Kit to track changes in cellular NAD levels (Xu et al., 2023). 10.1080/15376516.2023.2215862
- Synergistic Effect and Mechanism of Plumbagin with Gentamicin Against Carbapenem-Resistant Klebsiella pneumoniae.: The research highlights the synergistic antibacterial effects of plumbagin and gentamicin, with the NAD+/NADH Assay Kit being used to evaluate the metabolic impact on bacterial cells (Chen et al., 2020). 10.2147/IDR.S265753
- Cancer Research
- Neurodegenerative Research
- Age/Geriatric Related Disease Research
Características y beneficios
Simplified Process: Experience a streamlined process with the addition of only a single working reagent and a 10 minute room temperature reaction, reducing complexity and saving valuable time and effort.
Compatibility with High-Throughput Systems: Easily incorporate our kit into high-throughput handling systems, ensuring smooth and accurate processing, enhancing efficiency in your laboratory workflow.
Idoneidad
Principio
Otras notas
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Met. Corr. 1
Código de clase de almacenamiento
8B - Non-combustible corrosive hazardous materials
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Can this kit be used for detection of NADH levels in bacteria culture?
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Is there any antibody epitope information available for the products IL-12p40 and IL-12p70?
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For IL-12p40, the capture and detection antibodies are mouse monoclonal anti-human IL-12p40. As for IL-12p70, the capture antibody is rat monoclonal anti-human IL-12p70, and the detection antibody is mouse monoclonal anti-human IL-12p70. However, there is no available information on antibody binding domains.
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Can a white plate be used instead of a black plate for this assay?
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A black, opaque, flat-bottomed plate is recommended for fluorescence assays, and a black plate with a clear bottom is also acceptable. White plates are not recommended for fluorescence assays as they can increase background and cross-talk. An example of a recommended plate type for fluorescence assays is the product M9685.
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Does this assay measure total NAD+/NADH concentrations? If so, How can the conversion to NAD+ or NADH only be achieved?
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The calculation method is the same for NAD+ and NADH. However, there should be one well for the NAD+ test and another well for the NADH test. If the intention is to solely measure NAD+, the sample should be processed according to the NAD+ instructions. This involves homogenizing the sample with NAD+ extraction buffer, then proceeding with heating and addition of the assay buffer followed by the addition of the opposite buffer (in this case, NAD extraction buffer). The order of addition of the extraction buffers determines whether NAD+ or NADH is being measured, as it degrades the other due to the extraction pH.
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Is this kit's sample only for cultured cells? Do you have any data or protocols for serum, urine, saliva, etc.?
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This kit has not been tested with serum or urine samples. Unfortuantely, publications regarding this application could not found.
However, there may not be any problems with using plasma, as well as serum, with the kit. It is prudent to test a number of dilutions of urine to determine the best concentration to use in the assay. The following substances interfere with the assay and should be avoided in sample preparation: EDTA (>0.5 mM), ascorbic acid, SDS (>0.2%), sodium azide, NP-40 (>1%) and Tween-20 (>1%).Helpful?
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