Fluorescein Diphosphate, Tetraammonium Salt (FDP)
Fluorescein Diphosphate, Tetraammonium Salt (FDP)
Invitrogen™

Fluorescein Diphosphate, Tetraammonium Salt (FDP)

FDP is a colorless and nonfluorescent substrate for alkaline phosphatases. Sequential alkaline phosphatase mediated hydrolysis of its two phosphate substituentsRead more
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Catalog NumberQuantity
F29995 mg
Catalog number F2999
Price (BRL)
4.234,37
Each
Add to cart
Quantity:
5 mg
Price (BRL)
4.234,37
Each
Add to cart
FDP is a colorless and nonfluorescent substrate for alkaline phosphatases. Sequential alkaline phosphatase mediated hydrolysis of its two phosphate substituents yields weakly fluorescent fluorescein monophosphate followed by strongly fluorescent fluorescein (excitation/emission ∼490/514 nm).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Excitation/Emission490⁄514
For Use With (Equipment)Fluorometer, Microplate Reader
Label or DyeFITC (Fluorescein)
Quantity5 mg
Shipping ConditionRoom Temperature
SubstratePhosphatase Substrate
Detection MethodFluorescence
FormPowder
Substrate PropertiesChemical Substrate
Target EnzymeAlkaline Phosphatase, Tyrosine Phosphatases
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C).

Citations & References (37)

Citations & References
Abstract
Glibenclamide prevents increased extracellular matrix formation induced by high glucose concentration in mesangial cells.
Authors:Giannico G, Cortes P, Baccora MH, Hassett C, Taube DW, Yee J
Journal:Am J Physiol Renal Physiol
PubMed ID:16896180
'Other than stimulation of cell contractility, little is known about the potential metabolic effects induced by sulfonylureas, independently of insulin action. Previous studies from our laboratory demonstrated complete abrogation of glomerulosclerosis in an experimental model of type 1 diabetes chronically (9 mo) treated with low-dose sulfonylureas (Biederman JI, Vera E, ... More
Negative regulation of EGFR signalling through integrin-alpha1beta1-mediated activation of protein tyrosine phosphatase TCPTP.
Authors:Mattila E, Pellinen T, Nevo J, Vuoriluoto K, Arjonen A, Ivaska J
Journal:Nat Cell Biol
PubMed ID:15592458
'Integrin-mediated cell adhesion regulates a multitude of cellular responses, including proliferation, survival and cross-talk between different cellular signalling pathways. So far, integrins have been mainly shown to convey permissive signals enabling anchorage-dependent receptor tyrosine kinase signalling. Here we show that a collagen-binding integrin alpha(1)beta(1) functions as a negative regulator of ... More
Functional screening of intracellular proteins in single cells and in patterned cell arrays using electroporation.
Authors:Nolkrantz K, Farre C, Hurtig KJ, Rylander P, Orwar O
Journal:Anal Chem
PubMed ID:12199607
'A tool for detection and characterization of intracellular enzyme-substrate and receptor-ligand interactions inside the cytoplasm of single targeted cells or small confined groups of cells is presented. Fluorogenic enzyme substrates and receptor ligands were rapidly delivered by electroosmosis and internalized by electroporation in cells using an electrolyte-filled capillary (EFC) biased ... More
Randomly ordered addressable high-density optical sensor arrays.
Authors:Michael KL, Taylor LC, Schultz SL, Walt DR
Journal:Anal Chem
PubMed ID:9553489
'Array-based sensors provide an architecture for multianalyte sensing. In this paper, we report a new approach for array fabrication. Sensors are made by immobilizing different reactive chemistries on the surfaces of microspheres. Sensor arrays are prepared by randomly distributing a mixture of microsphere sensors on an optical substrate containing thousands ... More
In vivo imaging of tumors with protease-activated near-infrared fluorescent probes.
Authors:Weissleder R, Tung CH, Mahmood U, Bogdanov A
Journal:Nat Biotechnol
PubMed ID:10207887
'We have developed a method to image tumor-associated lysosomal protease activity in a xenograft mouse model in vivo using autoquenched near-infrared fluorescence (NIRF) probes. NIRF probes were bound to a long circulating graft copolymer consisting of poly-L-lysine and methoxypolyethylene glycol succinate. Following intravenous injection, the NIRF probe carrier accumulated in ... More