FLAA
Adenosine 5′-triphosphate (ATP) Bioluminescent Assay Kit
for ATP quantitation
Synonym(s):
ATP Bioluminescence Assay, ATP Determination Kit, Luminescent ATP Detection kit
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About This Item
EC Number:
213-579-1
NACRES:
NA.26
eCl@ss:
32160414
UNSPSC Code:
41116133
storage temp.
−20°C
Quality Level
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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.
Kit Components Also Available Separately
Product No.
Description
SDS
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
wgk
WGK 3
Storage Class
11 - Combustible Solids
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Environmental toxicology and pharmacology, 40(1), 206-214 (2015-07-06)
Fipronil is an insecticide extensively used to control pests in crops and animals. There are relates of poisoning due to exposure of fipronil in mammals and the liver has been suggested as potential target. In this study, we evaluated the
John F C Steele et al.
PloS one, 14(8), e0221226-e0221226 (2019-08-29)
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
Xi Zoë Zhong et al.
The Journal of physiology, 594(15), 4253-4266 (2016-08-02)
SLC17A9 proteins function as a lysosomal ATP transporter responsible for lysosomal ATP accumulation. P2X4 receptors act as lysosomal ion channels activated by luminal ATP. SLC17A9-mediated ATP transport across the lysosomal membrane is suppressed by Bafilomycin A1, the V-ATPase inhibitor. SLC17A9
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
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