CS0740
Acid phosphatase Assay Kit
1 kit sufficient for 1,000 assays (multiwell plates), 1 kit sufficient for 100 assays (tubes)
Synonym(s):
Acid Phosphatase Enzyme Activity Kit
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About This Item
UNSPSC Code:
12161503
NACRES:
NA.84
eCl@ss:
42010102
Product Name
Acid phosphatase Assay Kit, 1 kit sufficient for 1,000 assays (multiwell plates), 1 kit sufficient for 100 assays (tubes)
usage
kit sufficient for 1,000 assays (multiwell plates)
kit sufficient for 100 assays (tubes)
shipped in
dry ice
storage temp.
−20°C
Quality Level
Related Categories
Application
The kit is used for the detection of acid phosphatase activity in tissues, whole cell extracts, column fractions and purified enzyme. The kit contains all the reagents required for a fast and simple acid phosphatase detection. The kit contains a standard solution and a control enzyme.
Biochem/physiol Actions
Acid phosphatase is one of the acid hydrolases that normally reside in lysosomes. It is a marker for the identification of lysosomes in sub-cellular fractionations.
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - STOT RE 2 Oral
target_organs
Liver,Kidney
Storage Class
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
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Yuan Li et al.
The Journal of cell biology, 215(2), 167-185 (2016-11-05)
Lysosomes degrade macromolecules and recycle metabolites as well as being involved in diverse processes that regulate cellular homeostasis. The lysosome is limited by a single phospholipid bilayer that forms a barrier to separate the potent luminal hydrolases from other cellular
Henning Staedt et al.
Head & face medicine, 16(1), 35-35 (2020-12-09)
The aim was to compare early biochemical and histological osseous healing of chronic mandibular defects regenerated with bovine bone substitute with and without collagen membrane in vivo. Eight weeks after formation of a lateral full-thickness perforating bone defect in the
Cheng-Yen Lu et al.
Age (Dordrecht, Netherlands), 37(2), 33-33 (2015-04-13)
Ambient temperature reduction (ATR) can extend the lifespan of organisms, but the underlying mechanism is poorly understood. In this study, cellular degradation activity was evaluated in the muscle of an annual fish (Nothobranchius rachovii) reared under high (30 °C), moderate (25 °C)
Hua Zhao et al.
Journal of neuroscience methods, 217(1-2), 67-74 (2013-04-24)
Cobalamin (Cbl) utilization as a cofactor for methionine synthase and methylmalonyl-CoA mutase is dependent on the transport of Cbl through lysosomes and its subsequent delivery to the cytosol and mitochondria. We speculated that neuropathological conditions that impair lysosomal function (e.g.
Cameron G McCarthy et al.
American journal of physiology. Heart and circulatory physiology, 317(5), H1013-H1027 (2019-08-31)
Insufficient autophagy has been proposed as a mechanism of cellular aging, as this leads to the accumulation of dysfunctional macromolecules and organelles. Premature vascular aging occurs in hypertension. In fact, many factors that contribute to the deterioration of vascular function
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