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Perfluoroundecanoic acid-13C7

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Catalog No. TMIT-0536 Copy Product Info
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Perfluoroundecanoic acid-13C7 is a 13C-labeled version of Perfluoroundecanoic acid, which is a perfluoroalkyl substance (PFAS). It is an orally effective inducer of oxidative stress, promoting macrophage M2 polarization by activating the Wnt/β-catenin signaling pathway and enhancing nuclear accumulation of β-catenin. M2 phenotype macrophages induced by Perfluoroundecanoic acid accelerate tumor progression both in vitro and in vivo. The compound induces DNA damage and reproductive as well as pathophysiological dysfunction in male Swiss mice through oxidative stress. It also inhibits Leydig cell development in pubertal male rats via oxidative stress and autophagy (Autophagy) induction. Additionally, Perfluoroundecanoic acid accelerates insulitis development in a type 1 diabetic mouse model and is useful for research in ovarian cancer, type 1 diabetes, and inflammation.

Perfluoroundecanoic acid-13C7

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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Perfluoroundecanoic acid-13C7 is a 13C-labeled version of Perfluoroundecanoic acid, which is a perfluoroalkyl substance (PFAS). It is an orally effective inducer of oxidative stress, promoting macrophage M2 polarization by activating the Wnt/β-catenin signaling pathway and enhancing nuclear accumulation of β-catenin. M2 phenotype macrophages induced by Perfluoroundecanoic acid accelerate tumor progression both in vitro and in vivo. The compound induces DNA damage and reproductive as well as pathophysiological dysfunction in male Swiss mice through oxidative stress. It also inhibits Leydig cell development in pubertal male rats via oxidative stress and autophagy (Autophagy) induction. Additionally, Perfluoroundecanoic acid accelerates insulitis development in a type 1 diabetic mouse model and is useful for research in ovarian cancer, type 1 diabetes, and inflammation.
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year 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:
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2 Enter the in vivo formulation:
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%
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