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Bax inhibitor peptide V5 (Synonyms: BIP-V5, BAX Inhibiting Peptide V5)

Catalog No. T10463 Copy Product Info
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Bax inhibitor peptide V5 is a cell-penetrating pentapeptide and an inhibitor of Bax-induced apoptosis that specifically inhibits Bax-mediated mitochondria-dependent apoptosis. Bax inhibitor peptide V5 is primarily used in cancer research.

Bax inhibitor peptide V5

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Catalog No. T10463
Synonyms BIP-V5, BAX Inhibiting Peptide V5

Bax inhibitor peptide V5 is a cell-penetrating pentapeptide and an inhibitor of Bax-induced apoptosis that specifically inhibits Bax-mediated mitochondria-dependent apoptosis. Bax inhibitor peptide V5 is primarily used in cancer research.

Bax inhibitor peptide V5
Cas No. 579492-81-2
Pack SizePriceUSA StockGlobal StockQuantity
5 mg$877-10 days7-10 days
10 mg$1267-10 days7-10 days
25 mg$2677-10 days7-10 days
50 mg$4437-10 days7-10 days
100 mgInquiry7-10 days7-10 days
200 mgInquiry7-10 days7-10 days
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:Liquid
Color:White
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Product Introduction

Bioactivity
Description
Bax inhibitor peptide V5 is a cell-penetrating pentapeptide and an inhibitor of Bax-induced apoptosis that specifically inhibits Bax-mediated mitochondria-dependent apoptosis. Bax inhibitor peptide V5 is primarily used in cancer research.
In vitro
Methods: Human alveolar epithelial cell line A549 was treated with Bax inhibitor peptide V5 (200 μM). After 1 hour of pretreatment, bleomycin (120 mU/ml) was added, and the cells were incubated for a total of 24 hours. Cell apoptosis was then assessed.
Results: Pretreatment with Bax inhibitor peptide V5 significantly inhibited apoptosis in A549 cells and significantly reduced broleomycin-induced activated Bax expression. [1]
Method: Isolated mouse islets, dispersed into single cells, were treated with Bax inhibitor peptide V5 (100 μmol/L) and incubated for 24 hours; apoptosis was assessed by flow cytometry.
Results: Bax inhibitor peptide V5 significantly reduced the apoptosis rate of mouse islet cells. [2]
In vivo
Methods: To investigate the effects of the Bax inhibitor peptide V5 on bleomycin-induced lung injury, female C57BL/6J mice were used. Bleomycin (2 U/kg) and BIP-V5 (4 μmol/mouse) were administered intratracheally in a single dose (Day 0), and the animals were observed for 14 days.
Results: The 14-day cumulative survival rate was 75% in the Bax inhibitor peptide V5 group and 25% in the negative control peptide group, indicating a significant improvement in bleomycin-induced lung injury. [1]
Methods: To investigate the effects of Bax inhibitor peptide V5 combined with FGF-2 on early post-transplant islet survival, apoptosis, and inflammatory factors in the early post-transplant period, STZ-induced diabetic Balb/c mice were used. Bax inhibitor peptide V5 (100 μmol/L) and FGF-2 (100 ng) were encapsulated in gelatin microspheres, mixed with islets (150 IEQ), and transplanted subcapsularly into the kidney. PCR was performed 2 days later, and tissue was harvested 3 days later.
Results: The Bax inhibitor peptide V5 significantly improved the function of isolated islets in the mouse model and enhanced the function of transplanted islets.[2]
SynonymsBIP-V5, BAX Inhibiting Peptide V5
Chemical Properties
Molecular Weight586.79
FormulaC27H50N6O6S
Cas No.579492-81-2
SmilesC(N[C@H](C(N[C@H](C(N[C@@H](CCCCN)C(O)=O)=O)CC(C)C)=O)CCSC)(=O)[C@H]1N(C([C@H](C(C)C)N)=O)CCC1
Relative Density.1.185 g/cm3 (Predicted)
SequenceH-Val-Pro-Met-Leu-Lys-OH
Sequence ShortVPMLK
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
H2O: 80 mg/mL (136.33 mM), Sonication is recommended.
DMSO: 80 mg/mL (136.33 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2 mg/mL (3.41 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM1.7042 mL8.5209 mL17.0419 mL85.2094 mL
5 mM0.3408 mL1.7042 mL3.4084 mL17.0419 mL
10 mM0.1704 mL0.8521 mL1.7042 mL8.5209 mL
20 mM0.0852 mL0.4260 mL0.8521 mL4.2605 mL
50 mM0.0341 mL0.1704 mL0.3408 mL1.7042 mL
100 mM0.0170 mL0.0852 mL0.1704 mL0.8521 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
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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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