
Selank
Tuftsin-family heptapeptide with a Pro-Gly-Pro extension. Studied in GABAergic, enkephalin and neuroimmune signalling models.
Before you begin
- • Lot-matched certificate and laboratory notebook
- • Calibrated pipettes, low-binding tubes and suitable PPE
- • Validated solvent, assay reagents and model-specific SOP
- • Appropriate positive, negative and vehicle controls
Workflow
- 1Review the lot-matched COA and record identity, purity, batch number and received condition.
- 2Let the sealed vial equilibrate to room temperature before opening to limit condensation.
- 3Calculate the target stock concentration with C = mass / volume. Use only a solvent validated for the planned assay.
- 4Add solvent slowly down the vial wall, mix gently and avoid vortexing unless the validated method permits it.
- 5Prepare a log-spaced pilot concentration series; determine the usable range empirically instead of assuming a biological dose.
- 6Run the defined controls and technical replicates alongside every plate or experiment.
- 7Record preparation time, temperature, equipment, deviations and raw-data file locations.
Assay design
Pathway-specific readouts selected before preparation: GABAergic markers, enkephalin-degradation activity, or cytokine panels. Selecting the endpoint after seeing the data is the failure mode this compound's literature is prone to.
Required controls
- Vehicle-only negative control
- Untreated baseline
- Validated pathway control
- Parallel viability measurement
Reported protocol
- Standard
- 300 mcg to 500 mcg, afternoon or evening
- Route
- Intranasal or subcutaneous
- Cycle length
- 14 to 21 days on, followed by 7 to 14 days off
Diluent
Sterile bacteriostatic water (0.9% benzyl alcohol) for multi-withdrawal stock, or sterile water for injection where a preservative-free stock is required by the assay.
Reconstitution concentrations
Solvent volume sets the stock concentration for this 10 mg vial. Lower volume gives a more concentrated stock and smaller working aliquots; higher volume gives a more dilute stock that is easier to measure accurately.
| Solvent added | Stock concentration | Per 0.1 mL | Per unit (U-100) |
|---|---|---|---|
| 1 mL | 10 mg/mL | 1 mg | 100 mcg |
| 2 mL | 5 mg/mL | 500 mcg | 50 mcg |
| 3 mL | 3.33 mg/mL | 333.33 mcg | 33.33 mcg |
Working range
Neuronal and immune-cell work commonly runs the nanomolar to low-micromolar band.
Pathway-specific readouts selected before preparation: GABAergic markers, enkephalin-degradation activity, or cytokine panels. Selecting the endpoint after seeing the data is the failure mode this compound's literature is prone to.
Stability
- Lyophilized
- Stable sealed and dry at the certificate temperature.
- In solution
- Establish empirically for your solvent and container.
Handling notes
- Choose one primary endpoint and pre-register it.
- Where Semax is the comparator, run both in the same experiment.
- Use low-binding consumables for dilute stocks.
Documentation checklist
Record lot and COA, mass balance, solvent and concentration, preparation timestamp, storage history, plate map, replicate plan, instrument settings, exclusions and deviations. Preserve raw data and analysis code with the experiment record.
