FLAA
Adenosine 5′-triphosphate (ATP) Bioluminescent Assay Kit
for ATP quantitation
Sinónimos:
ATP Bioluminescence Assay, ATP Determination Kit, Luminescent ATP Detection kit
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About This Item
Productos recomendados
storage temp.
−20°C
General description
The Adenosine 5′-triphosphate (ATP) Bioluminescent Assay Kit may be employed for the quantitative bioluminescent determination of ATP in samples. ATP is consumed and light is emitted when luciferase catalyzes the oxidation of D-luciferin. When ATP is the limiting reagent, the light emitted is proportional to the ATP present in the sample.
Application
Adenosine 5′-triphosphate (ATP) Bioluminescent Assay Kit has also been used in the quantification of ATP in 3D matrixes of human neurons, hepatic cells with ischemia, various bacterial cultures and lysosomes.
Solo componentes del kit
Referencia del producto
Descripción
- FL-AAB Dilution buffer 1 mL/vial
- FL-AAM Assay mix 1 mL/vial
- FL-AAS ATP standard 1 mL/vial
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
10 - Combustible liquids
Certificados de análisis (COA)
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F Chen et al.
Journal of clinical microbiology, 32(11), 2791-2800 (1994-11-01)
A bioluminescent assay which employs the luciferin-luciferase ATP-dependent reaction was used to evaluate the viability of populations of Pneumocystis carinii derived from infected rat lungs. Contamination with host cells was reduced by a purification method which involved a combination of
Nadeshda Andreeva et al.
Applied microbiology and biotechnology, 102(12), 5235-5244 (2018-04-24)
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Yuri L Boteon et al.
PloS one, 14(10), e0224066-e0224066 (2019-10-24)
The combination of hypothermic and normothermic machine perfusion (HMP+NMP) of the liver provides individual benefits of both techniques, improving the rescue of marginal organs. The aim of this study was to investigate the effect on the bioenergetic status and the
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Witkowska A M, et al.
Journal of Food Research, 2(4), 37-37 (2013)
John F C Steele et al.
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Plant NLRs are modular immune receptors that trigger rapid cell death in response to attempted infection by pathogens. A highly conserved nucleotide-binding domain shared with APAF-1, various R-proteins and CED-4 (NB-ARC domain) is proposed to act as a molecular switch
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