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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.

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 5 mg | $87 | 7-10 days | 7-10 days | |
| 10 mg | $126 | 7-10 days | 7-10 days | |
| 25 mg | $267 | 7-10 days | 7-10 days | |
| 50 mg | $443 | 7-10 days | 7-10 days | |
| 100 mg | Inquiry | 7-10 days | 7-10 days | |
| 200 mg | Inquiry | 7-10 days | 7-10 days |
| 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] |
| Synonyms | BIP-V5, BAX Inhibiting Peptide V5 |
| Molecular Weight | 586.79 |
| Formula | C27H50N6O6S |
| Cas No. | 579492-81-2 |
| Smiles | C(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) |
| Sequence | H-Val-Pro-Met-Leu-Lys-OH |
| Sequence Short | VPMLK |
| Storage | Powder: -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
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. | ||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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