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ATPγS tetralithium salt

ATPγS tetralithium salt
ATPγS tetralithium salt is a good substrate for RNA-stimulated nucleotide hydrolysis and RNA unwinding activity of eIF4A.
Catalog No. T22592Cas No. 93839-89-5
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Purity:90%
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ATPγS tetralithium salt

Purity: 90%
Catalog No. T22592Alias ATP-gamma-S tetralithium saltCas No. 93839-89-5

ATPγS tetralithium salt is a good substrate for RNA-stimulated nucleotide hydrolysis and RNA unwinding activity of eIF4A.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$148In Stock
5 mg$372In Stock
10 mg$519In Stock
25 mg$892In Stock
50 mg$1,280In Stock
100 mg$1,780In Stock
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Product Introduction

Bioactivity
Description
ATPγS tetralithium salt is a good substrate for RNA-stimulated nucleotide hydrolysis and RNA unwinding activity of eIF4A.
In vitro
ATPγS tetralithium salt enhances intrinsic fluorescence and induces aggregation, thereby increasing spinach Rubisco activating enzyme activity. The concentration dependence of the ATPγS tetralithium salt effect is S-shaped, but at pH 8, the half-saturation requirement of ATPγS tetralithium salt (12 μM) is consistent with that measured indirectly using the fluorescent probe 1-anilinolyl-8-sulfonate. The binding affinities (6 μM) are not much different. [2]
In vivo
METHODS: A mouse model of ALI induced by intratracheal administration of endotoxin/lipopolysaccharide (LPS) and cultured lung ECs was used and treated with ATPγS tetralithium salt (50-100 μM final blood concentration).
RESULTS ATPγS tetralithium salt attenuated the inflammatory response, reduced the accumulation of cells (48%, P < 0.01) and proteins (57%, P < 0.01) in bronchoalveolar lavage fluid, and reduced neutrophil infiltration and Evans blue albumin dye extravasation into lung tissue. [3]
AliasATP-gamma-S tetralithium salt
Chemical Properties
Molecular Weight546.98
FormulaC10H12Li4N5O12P3S
Cas No.93839-89-5
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 100 mg/mL (182.82 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM1.8282 mL9.1411 mL18.2822 mL91.4110 mL
5 mM0.3656 mL1.8282 mL3.6564 mL18.2822 mL
10 mM0.1828 mL0.9141 mL1.8282 mL9.1411 mL
20 mM0.0914 mL0.4571 mL0.9141 mL4.5706 mL
50 mM0.0366 mL0.1828 mL0.3656 mL1.8282 mL
100 mM0.0183 mL0.0914 mL0.1828 mL0.9141 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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