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PA2-GNU7

Catalog No. TP4024 Copy Product Info
🥰Excellent
PA2-GNU7 is an antimicrobial peptide (AMP) with potent antibacterial activity, demonstrating minimum inhibitory concentrations (MIC) of 2 μM for Pseudomonas aeruginosa, 1 μM for Escherichia coli, 2 μM for Salmonella, 2 μM for Staphylococcus aureus, and 8 μM for Candida albicans. It rapidly and selectively kills Pseudomonas aeruginosa without affecting other symbiotic bacteria and significantly enhances the survival rate of mice infected with Pseudomonas aeruginosa. PA2-GNU7 has potential applications in researching and developing treatments for infections caused by multidrug-resistant Pseudomonas aeruginosa.

PA2-GNU7

Copy Product Info
🥰Excellent
Catalog No. TP4024

PA2-GNU7 is an antimicrobial peptide (AMP) with potent antibacterial activity, demonstrating minimum inhibitory concentrations (MIC) of 2 μM for Pseudomonas aeruginosa, 1 μM for Escherichia coli, 2 μM for Salmonella, 2 μM for Staphylococcus aureus, and 8 μM for Candida albicans. It rapidly and selectively kills Pseudomonas aeruginosa without affecting other symbiotic bacteria and significantly enhances the survival rate of mice infected with Pseudomonas aeruginosa. PA2-GNU7 has potential applications in researching and developing treatments for infections caused by multidrug-resistant Pseudomonas aeruginosa.

PA2-GNU7
Cas No. 2387505-19-1
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiryInquiryInquiry
50 mgInquiryInquiryInquiry
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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Product Introduction

Bioactivity
Description
PA2-GNU7 is an antimicrobial peptide (AMP) with potent antibacterial activity, demonstrating minimum inhibitory concentrations (MIC) of 2 μM for Pseudomonas aeruginosa, 1 μM for Escherichia coli, 2 μM for Salmonella, 2 μM for Staphylococcus aureus, and 8 μM for Candida albicans. It rapidly and selectively kills Pseudomonas aeruginosa without affecting other symbiotic bacteria and significantly enhances the survival rate of mice infected with Pseudomonas aeruginosa. PA2-GNU7 has potential applications in researching and developing treatments for infections caused by multidrug-resistant Pseudomonas aeruginosa.
In vitro
PA2-GNU7 (21 h) demonstrates potent antibacterial activity, with minimum inhibitory concentrations (MIC) against Pseudomonas aeruginosa, Escherichia coli, Salmonella spp., Staphylococcus aureus, and Candida albicans at 2 μM, 1 μM, 2 μM, 2 μM, and 8 μM, respectively. PA2-GNU7 (1 μM) selectively eradicates Pseudomonas aeruginosa in a dual-species culture (1:1 P. aeruginosa and E. coli or Salmonella).
In vivo
Administered intraperitoneally at a dose of PA2-GNU7 (15-25 mg/kg) 30 minutes post-infection, significantly enhances the survival rate of BALB/c mice infected with Pseudomonas aeruginosa.
Chemical Properties
Molecular Weight3372.17
FormulaC150H276N50O37
Cas No.2387505-19-1
SmilesC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC(CNC(CNC(CNC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CO)N)=O)CCC(N)=O)=O)CCCNC(=N)N)=O)CCCCN)=O)CC(C)C)=O)C)=O)C)=O)CCCCN)=O)CC(C)C)=O)[C@@H](C)O)=O)CO)=O)CCCCN)=O)=O)=O)=O)CCCNC(=N)N)=O)CC(C)C)=O)CC(C)C)=O)CCCNC(=N)N)(=O)N1[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CCCNC(=N)N)C(O)=O)=O)CC(C)C)=O)CCCCN)=O)CCC(N)=O)=O)CCCCN)=O)CC(C)C)=O)CC(C)C)=O)CCC(N)=O)=O)CC(C)C)=O)CC(C)C)=O)CCC1
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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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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