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Mu-6S-Palm-β-Glc

Catalog No. T37191 Copy Product Info
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Mu-6S-Palm-β-Glc is a fluorogenic substrate specifically designed for palmitoyl-protein thioesterase (PPT). It is enzymatically cleaved by PPT1 to release the fluorescent 4-methylumbelliferone (MU) moiety, enabling sensitive quantification of enzyme activity. This substrate is a critical tool in the study of infantile neuronal ceroid lipofuscinosis (INCL), a lysosomal storage disorder. It is utilized for both prenatal and postnatal diagnostic assays, as well as in the evaluation of bi-functional IgG-lysosomal enzyme fusion proteins for brain-targeted drug delivery.

Mu-6S-Palm-β-Glc

Copy Product Info
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Catalog No. T37191

Mu-6S-Palm-β-Glc is a fluorogenic substrate specifically designed for palmitoyl-protein thioesterase (PPT). It is enzymatically cleaved by PPT1 to release the fluorescent 4-methylumbelliferone (MU) moiety, enabling sensitive quantification of enzyme activity. This substrate is a critical tool in the study of infantile neuronal ceroid lipofuscinosis (INCL), a lysosomal storage disorder. It is utilized for both prenatal and postnatal diagnostic assays, as well as in the evaluation of bi-functional IgG-lysosomal enzyme fusion proteins for brain-targeted drug delivery.

Mu-6S-Palm-β-Glc
Cas No. 229644-17-1
Pack SizePriceUSA StockGlobal StockQuantity
500 μg$148-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Mu-6S-Palm-β-Glc is a fluorogenic substrate specifically designed for palmitoyl-protein thioesterase (PPT). It is enzymatically cleaved by PPT1 to release the fluorescent 4-methylumbelliferone (MU) moiety, enabling sensitive quantification of enzyme activity. This substrate is a critical tool in the study of infantile neuronal ceroid lipofuscinosis (INCL), a lysosomal storage disorder. It is utilized for both prenatal and postnatal diagnostic assays, as well as in the evaluation of bi-functional IgG-lysosomal enzyme fusion proteins for brain-targeted drug delivery.
In vitro
Mu-6S-Palm-β-Glc is a highly sensitive fluorogenic substrate for rapid PPT1 activity detection in cells or tissues. Fluorescence changes accurately reflect PPT1 deficiency in INCL samples, making it a standard tool for diagnosis and enzyme replacement monitoring. β-glucosidase co-administration enhances assay efficiency [1][2]。
Chemical Properties
Molecular Weight592.78
FormulaC32H48O8S
Cas No.229644-17-1
SmilesCC=1C=2C(=CC(O[C@@H]3O[C@H](CSC(CCCCCCCCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]3O)=CC2)OC(=O)C1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 24 mg/mL (40.49 mM), Sonication is recommended.
DMF: 15 mg/mL (25.3 mM), Sonication is recommended.
Solution Preparation Table
DMF/DMSO
1mg5mg10mg50mg
1 mM1.6870 mL8.4348 mL16.8697 mL84.3483 mL
5 mM0.3374 mL1.6870 mL3.3739 mL16.8697 mL
10 mM0.1687 mL0.8435 mL1.6870 mL8.4348 mL
20 mM0.0843 mL0.4217 mL0.8435 mL4.2174 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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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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