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AF 568 carboxylic acid

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Catalog No. T208614

AF 568 carboxylic acid is a non-reactive form of the orange fluorescent dye AF 568. It exhibits an absorption wavelength range of 590-720 nm (FRET) and an emission wavelength range of 515-720 nm. AF 568 alkyne can form stable covalent bonds with amino-containing molecules through its carboxylic acid group. It can also participate in a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing alkyne groups. Additionally, it is capable of engaging in strain-promoted azide-alkyne cycloaddition (SPAAC) with compounds containing DBCO or BCN groups.

AF 568 carboxylic acid

AF 568 carboxylic acid

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Catalog No. T208614
AF 568 carboxylic acid is a non-reactive form of the orange fluorescent dye AF 568. It exhibits an absorption wavelength range of 590-720 nm (FRET) and an emission wavelength range of 515-720 nm. AF 568 alkyne can form stable covalent bonds with amino-containing molecules through its carboxylic acid group. It can also participate in a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing alkyne groups. Additionally, it is capable of engaging in strain-promoted azide-alkyne cycloaddition (SPAAC) with compounds containing DBCO or BCN groups.
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Product Introduction

Bioactivity
Description
AF 568 carboxylic acid is a non-reactive form of the orange fluorescent dye AF 568. It exhibits an absorption wavelength range of 590-720 nm (FRET) and an emission wavelength range of 515-720 nm. AF 568 alkyne can form stable covalent bonds with amino-containing molecules through its carboxylic acid group. It can also participate in a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing alkyne groups. Additionally, it is capable of engaging in strain-promoted azide-alkyne cycloaddition (SPAAC) with compounds containing DBCO or BCN groups.
Chemical Properties
FormulaC33H28K2N2O11S2
Storage & Solubility Information
Storagekeep away from direct sunlight | store at -20°C | Shipping with blue ice/Shipping at ambient temperature.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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