VIP

VIP

Note:
  • USA MADE 2-7 days delivery
  • International 5-20 days delivery
Out of stock

Product Overview

A core principle in systemic cell signaling research dictates that exploring advanced vasoactive compounds demands both uncompromised structural integrity and verification of chemical purity. The VIP formulation satisfies these rigorous requirements, serving as a highly refined regulatory neuropeptide engineered for precise laboratory investigation into cardiovascular, pulmonary, and immune system dynamics. Each vial delivers pure Vasoactive Intestinal Peptide (VIP), stabilized as a vacuum freeze-dried (lyophilized) powder with a verified purity profile exceeding 98%.

VIP is an endogenous 28-amino acid neuropeptide belonging to the glucagon-secretin superfamily. To optimize its utility in experimental models, its structural sequence is meticulously synthesized to preserve the exact linear architecture required for high-affinity receptor binding. Unlike large, dense proteins that require complex breakdown, its fractional peptide size enables it to pass easily through cellular environments to interface directly with target receptor sites without triggering non-specific immune responses. The compound is defined by its specific primary sequence configuration and optimized for stability in vitro.

Operating as a broad-spectrum regulatory molecule, VIP acts as a potent agonist at specific G-protein coupled receptors, primarily VPAC1 and VPAC2, distributed throughout the central nervous system, smooth muscle tissues, and immune cells. It interfaces directly with these receptors to activate adenylate cyclase pathways, elevating intracellular cyclic adenosine monophosphate (cAMP) levels. Documented research indicates that VIP triggers profound smooth muscle relaxation, induces vascular dilation, and modulates inflammatory cytokine cascades, permitting the detailed investigation of targeted vascular homeostatic mechanisms and neuro-immune interactions in controlled laboratory settings.

Product Specifications

  • Form: Lyophilized (vacuum freeze-dried) powder
  • Purity: Greater than 98% (verified by HPLC analysis)
  • Peptide Class: Vasoactive Intestinal Peptide (28-amino acid sequence)
  • Primary Targets: VPAC1 and VPAC2 Receptors
  • Target Systems: Cardiovascular, Pulmonary, and Immune Pathways

Container Specifications

The physical attributes of the storage vessel directly impact the shelf life of the compound. All research environments should utilize clean, chemically inert containers. Glass vials provide the highest level of protection against gas permeability and chemical interaction, though high-density polypropylene tubes serve as a valid alternative. Keep all stored peptides away from automatic frost-free freezers, as their internal defrost cycles create regular temperature swings that compromise peptide longevity.

Storage and Handling Protocols

Maintaining the biological utility of a high-purity regulatory neuropeptide requires strict adherence to environmental controls. Because peptide bonds are highly sensitive to thermal, atmospheric, and oxidative degradation, researchers must follow specific preservation guidelines to protect the structural integrity of the compound.

Lyophilized Powder Preservation

Unopened, lyophilized vials must be kept in long-term cold storage at a stable temperature of -20°C. For extended storage timelines exceeding one year, maintaining a temperature of -80°C is highly recommended to completely arrest baseline molecular degradation. Vials should remain housed in sealed, light-shielded containers to prevent degradation from ultraviolet exposure and atmospheric moisture.

Before opening a vial or introducing a reconstitution solvent, allow the container to sit at room temperature until it fully equilibrates. Skipping this step introduces a substantial risk of moisture condensation forming on the cold powder, which immediately accelerates enzymatic breakdown.

Properly stored at -20°C, the lyophilized powder remains stable and viable for a period of 2 to 4 years.

For optimal preservation, utilize airtight glass vials equipped with PTFE-lined caps. If a vial is opened to remove fractional quantities, the remaining headspace should be flushed with an inert gas like dry nitrogen or argon before resealing to minimize oxidative risk, especially given the presence of oxidation-sensitive residues within the 28-amino acid chain.

Reconstituted Solution Stability

Once transitioned into a liquid state, the neuropeptide becomes significantly more fragile. Reconstituted VIP solutions must be kept under continuous refrigeration at 2-8°C and should be completely utilized within 30 days. If your experimental timeline requires keeping the liquid compound past this threshold, divide the freshly mixed solution into single-use aliquots immediately after reconstitution and freeze them at -20°C or -80°C.

To maintain maximum stability, employ sterile, neutral or slightly acidic buffers or sterile water. Repeated freeze-thaw cycles must be strictly avoided, as the physical stress of phase changes causes structural shearing of the linear peptide chain.

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At PeptideHubs, scientific integrity and product reliability are at the core of everything we do. Each compound is manufactured and tested under strict quality control protocols to ensure consistency, purity, and performance for research applications.

However, if for any reason our product does not meet your research expectations, we offer a 60-day money-back guarantee — providing a risk-free procurement experience for qualified researchers and institutions.

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