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Peptide P2.2

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Catalog No. TP3855

Peptide P2.2, a non-ribosomal antimicrobial peptide, exhibits potent antibacterial activity, with an MIC50 of 4 μM against V. parahaemolyticus and 32 μM against V. alginolyticus. This peptide enhances the synergistic antimicrobial effects when used in conjunction with antibiotics (e.g., Ofloxacin and Linezolid) and shows negligible hemolytic activity. Peptide P2.2 disrupts bacterial membranes and increases their permeability by modulating proteins involved in the type VI and type III secretion systems. It is applicable in bacterial infection research.

Peptide P2.2

Peptide P2.2

😃Good
Catalog No. TP3855
Peptide P2.2, a non-ribosomal antimicrobial peptide, exhibits potent antibacterial activity, with an MIC50 of 4 μM against V. parahaemolyticus and 32 μM against V. alginolyticus. This peptide enhances the synergistic antimicrobial effects when used in conjunction with antibiotics (e.g., Ofloxacin and Linezolid) and shows negligible hemolytic activity. Peptide P2.2 disrupts bacterial membranes and increases their permeability by modulating proteins involved in the type VI and type III secretion systems. It is applicable in bacterial infection research.
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Product Introduction

Bioactivity
Description
Peptide P2.2, a non-ribosomal antimicrobial peptide, exhibits potent antibacterial activity, with an MIC50 of 4 μM against V. parahaemolyticus and 32 μM against V. alginolyticus. This peptide enhances the synergistic antimicrobial effects when used in conjunction with antibiotics (e.g., Ofloxacin and Linezolid) and shows negligible hemolytic activity. Peptide P2.2 disrupts bacterial membranes and increases their permeability by modulating proteins involved in the type VI and type III secretion systems. It is applicable in bacterial infection research.
Chemical Properties
Storage & Solubility Information
Storagekeep away from moisture | Powder: -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 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% Saline/PBS/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 μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
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% 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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