SNAP-8 peptide is a laboratory-developed compound derived from research on cellular communication mechanisms, particularly those involved in signal transmission between cells. It is designed for controlled experimental use and is commonly included in studies exploring how short peptides may influence coordinated cellular activity.
SNAP-8 acetyl peptide has been studied in models of neuromuscular signaling and surface-level cellular interactions, providing insights into how communication pathways function under specific research conditions.
SNAP-8 (10mg) Key Features & Specs
SNAP-8 (10mg) is a structured research peptide designed for use in controlled laboratory settings focused on cellular signaling. Its consistent composition and verified analytical profile support reproducibility across experimental conditions. The following specifications provide essential identifiers to guide proper handling and integration into study protocols.
- Subcategory: Aesthetic & Cosmetic Peptides
- Strength: 10mg
- CAS: 868844-74-0
- Chemical Formula: C₄₁H₇₀N₁₆O₁₆S
- Molecular Weight: 1075.16 g/mol
- Peptide Sequence: Acetyl-Glu-Glu-Met-Gln-Arg-Arg-Ala-Asp-NH2
- Synonyms: Acetyl Octapeptide-3
For laboratory research use only.
SNAP-8 (10mg) Research Uses
SNAP-8 research explores how short-chain peptides may influence coordinated cellular signaling, particularly in models involving communication between nerve and muscle cells. In controlled studies, it has been examined for its potential to affect processes linked to signal transmission and cellular responsiveness.
SNAP-8 octapeptide research is also applied in surface-level biological models, where changes in cell-to-cell interaction and structural behavior are observed. These research efforts help clarify how signaling peptides may regulate cellular activity under experimental conditions.
SNAP-8 (10mg) Insights & Observed Findings
In vitro studies involving SNAP-8 (10mg) commonly assess activity in the micromolar range, depending on the specific model and objectives. Reported observations include shifts in signaling patterns and variations in how cells respond to external stimuli in controlled environments.
The SNAP-8 peptide has also been evaluated in comparative settings to better understand its behavior relative to similar compounds. These findings remain preliminary and are primarily used to inform further experimental design and investigation.
SNAP-8 (10mg) Handling & Storage
Store SNAP-8 (10mg) in a freezer at –20°C under standard laboratory conditions. Ensure the material is kept away from light, moisture, and excess heat prior to preparation.
For reconstitution, use sterile solvents and follow proper laboratory handling procedures during handling. Once prepared, keep the solution refrigerated and minimize handling variability, including repeated freeze-thaw cycles, during storage and handling.
Compliance Notice: This product is intended for laboratory research use only and is not approved for human or veterinary use. It is not intended for diagnostic, therapeutic, or clinical applications. Any reference to biological activity or potential effects is based solely on preclinical or in-vitro findings and should not be interpreted as validated clinical outcomes. Researchers are responsible for ensuring proper handling, storage, and disposal in accordance with institutional, federal, and international guidelines.
References
- Tafoya LCR, Mameli M, Miyashita T, Guzowski JF, Valenzuela CF, Wilson MC. Expression and function of SNAP-25 as a universal SNARE component in GABAergic neurons. Journal of Neuroscience. 2006;26(30):7826-7838. doi:10.1523/jneurosci.1866-06.2006
- Errante F, Ledwoń P, Latajka R, Rovero P, Papini AM. Cosmeceutical peptides in the framework of sustainable Wellness economy. Frontiers in Chemistry. 2020;8:572923. doi:10.3389/fchem.2020.572923
- Khvotchev M, Soloviev M. SNARE modulators and SNARE mimetic peptides. Biomolecules. 2022;12(12):1779. doi:10.3390/biom12121779
- Fasshauer D, Margittai M. A transient n-terminal interaction of SNAP-25 and Syntaxin nucleates SNARE assembly. Journal of Biological Chemistry. 2004;279(9):7613-7621. doi:10.1074/jbc.m312064200