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A new enzymatic assay to quantify inorganic pyrophosphate in plasma
by
Niaziorimi, Fatemeh
, Szeri, Flora
, Johansson, Gunnar
, Jansen, Robert S.
, Lundkvist, Stefan
, Caffet, Matthew
, Terry, Sharon F.
, van de Wetering, Koen
in
Adenosine Triphosphate
/ Analytical Chemistry
/ Animal models
/ Animals
/ Assaying
/ ATP sulfurylase
/ Biochemistry
/ Bioluminescence
/ Blood plasma
/ blood sampling
/ Calcification
/ Calcification (ectopic)
/ Calcinosis
/ Characterization and Evaluation of Materials
/ Chemical properties
/ Chemistry
/ Chemistry and Materials Science
/ Composition
/ Deregulation
/ diabetes
/ Diabetes mellitus
/ Diphosphates
/ Ectopic mineralization
/ Ethylenediaminetetraacetic acids
/ filtration
/ Food Science
/ Homeostasis
/ Humans
/ Identification and classification
/ Kidney diseases
/ Laboratory Medicine
/ Lampyridae
/ luciferase
/ Luciferases, Firefly
/ Membranes
/ Mineralization
/ Mineralization inhibitor
/ Molecular weight
/ Monitoring/Environmental Analysis
/ Phosphates
/ Plasma
/ Pyrophosphate
/ Rats
/ Research Paper
/ Soft tissues
/ sulfate adenylyltransferase
/ tissues
/ Vascular calcification
/ Weight reduction
2023
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A new enzymatic assay to quantify inorganic pyrophosphate in plasma
by
Niaziorimi, Fatemeh
, Szeri, Flora
, Johansson, Gunnar
, Jansen, Robert S.
, Lundkvist, Stefan
, Caffet, Matthew
, Terry, Sharon F.
, van de Wetering, Koen
in
Adenosine Triphosphate
/ Analytical Chemistry
/ Animal models
/ Animals
/ Assaying
/ ATP sulfurylase
/ Biochemistry
/ Bioluminescence
/ Blood plasma
/ blood sampling
/ Calcification
/ Calcification (ectopic)
/ Calcinosis
/ Characterization and Evaluation of Materials
/ Chemical properties
/ Chemistry
/ Chemistry and Materials Science
/ Composition
/ Deregulation
/ diabetes
/ Diabetes mellitus
/ Diphosphates
/ Ectopic mineralization
/ Ethylenediaminetetraacetic acids
/ filtration
/ Food Science
/ Homeostasis
/ Humans
/ Identification and classification
/ Kidney diseases
/ Laboratory Medicine
/ Lampyridae
/ luciferase
/ Luciferases, Firefly
/ Membranes
/ Mineralization
/ Mineralization inhibitor
/ Molecular weight
/ Monitoring/Environmental Analysis
/ Phosphates
/ Plasma
/ Pyrophosphate
/ Rats
/ Research Paper
/ Soft tissues
/ sulfate adenylyltransferase
/ tissues
/ Vascular calcification
/ Weight reduction
2023
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A new enzymatic assay to quantify inorganic pyrophosphate in plasma
by
Niaziorimi, Fatemeh
, Szeri, Flora
, Johansson, Gunnar
, Jansen, Robert S.
, Lundkvist, Stefan
, Caffet, Matthew
, Terry, Sharon F.
, van de Wetering, Koen
in
Adenosine Triphosphate
/ Analytical Chemistry
/ Animal models
/ Animals
/ Assaying
/ ATP sulfurylase
/ Biochemistry
/ Bioluminescence
/ Blood plasma
/ blood sampling
/ Calcification
/ Calcification (ectopic)
/ Calcinosis
/ Characterization and Evaluation of Materials
/ Chemical properties
/ Chemistry
/ Chemistry and Materials Science
/ Composition
/ Deregulation
/ diabetes
/ Diabetes mellitus
/ Diphosphates
/ Ectopic mineralization
/ Ethylenediaminetetraacetic acids
/ filtration
/ Food Science
/ Homeostasis
/ Humans
/ Identification and classification
/ Kidney diseases
/ Laboratory Medicine
/ Lampyridae
/ luciferase
/ Luciferases, Firefly
/ Membranes
/ Mineralization
/ Mineralization inhibitor
/ Molecular weight
/ Monitoring/Environmental Analysis
/ Phosphates
/ Plasma
/ Pyrophosphate
/ Rats
/ Research Paper
/ Soft tissues
/ sulfate adenylyltransferase
/ tissues
/ Vascular calcification
/ Weight reduction
2023
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A new enzymatic assay to quantify inorganic pyrophosphate in plasma
Journal Article
A new enzymatic assay to quantify inorganic pyrophosphate in plasma
2023
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Overview
Inorganic pyrophosphate (PPi) is a crucial extracellular mineralization regulator. Low plasma PPi concentrations underlie the soft tissue calcification present in several rare hereditary mineralization disorders as well as in more common conditions like chronic kidney disease and diabetes. Even though deregulated plasma PPi homeostasis is known to be linked to multiple human diseases, there is currently no reliable assay for its quantification. We here describe a PPi assay that employs the enzyme ATP sulfurylase to convert PPi into ATP. Generated ATP is subsequently quantified by firefly luciferase–based bioluminescence. An internal ATP standard was used to correct for sample-specific interference by matrix compounds on firefly luciferase activity. The assay was validated and shows excellent precision (< 3.5%) and accuracy (93–106%) of PPi spiked into human plasma samples. We found that of several anticoagulants tested only EDTA effectively blocked conversion of ATP into PPi in plasma after blood collection. Moreover, filtration over a 300,000-Da molecular weight cut-off membrane reduced variability of plasma PPi and removed ATP present in a membrane-enclosed compartment, possibly platelets. Applied to plasma samples of wild-type and
Abcc6
−/−
rats, an animal model with established low circulating levels of PPi, the new assay showed lower variability than the assay that was previously in routine use in our laboratory. In conclusion, we here report a new and robust assay to determine PPi concentrations in plasma, which outperforms currently available assays because of its high sensitivity, precision, and accuracy.
Graphical Abstract
Publisher
Springer Berlin Heidelberg,Springer,Springer Nature B.V
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