Selank is a synthetic heptapeptide derivative of human tuftsin evaluated in preclinical neurochemical research. PX1 Research provides analytical-grade Selank for laboratory research, backed by USA-based synthesis, lot-specific HPLC/MS and endotoxin COAs, and same-day domestic shipping from California and Arizona facilities for qualified research institutions.
Selank is a synthetic heptapeptide derivative of human tuftsin evaluated in preclinical neurochemical research. PX1 Research provides analytical-grade Selank for laboratory research, backed by USA-based synthesis, lot-specific HPLC/MS and endotoxin COAs, and same-day domestic shipping from California and Arizona facilities for qualified research institutions.
Selank (sequence: Thr-Lys-Pro-Arg-Pro-Gly-Pro) is a synthetic regulatory peptide engineered by elongating the sequence of the naturally occurring immunomodulatory peptide tuftsin. Preclinical models demonstrate that Selank influences central neurotransmission by modulating GABAergic signaling, inhibiting enkephalin-degrading enzymes, and altering monoamine levels in central tissue. Unlike classical benzodiazepine receptor agonists, Selank interacts with allosteric modulatory sites without binding directly to the primary GABA recognition site. Researchers frequently evaluate Selank alongside related compounds like Semax to study neuroplasticity, neuroprotection, and peptide stability in vitro.
When purchasing reference material for laboratory experiments, verifying batch-level analytical data is critical. Researchers can access detailed analytical documentation and order 10 mg vials of Selank with verified identity and purity directly through PX1 Research.
Selank is a synthetic analog of the naturally occurring tetrapeptide tuftsin (Thr-Lys-Pro-Arg), extended at the C-terminus by a tripeptide sequence (Pro-Gly-Pro) to enhance metabolic stability. The chemical structure of Selank features the amino acid sequence L-Threonyl-L-lysyl-L-prolyl-L-arginyl-L-prolyl-glycyl-L-proline. The addition of the C-terminal Pro-Gly-Pro fragment significantly retards enzymatic degradation by serum carboxypeptidases and endopeptidases, extending its active biological half-life in aqueous and cellular environments compared to native tuftsin.
Originally synthesized at the Institute of Molecular Genetics of the Russian Academy of Sciences, Selank belongs to a structural class of regulatory peptides designed to integrate immunomodulatory and neurotropic actions. In pure isolated form, Selank presents as a white lyophilized powder with a molecular weight of approximately 751.9 g/mol. To review structural assay data and technical specifications, researchers can explore our complete Selank research hub.
Because small peptides are susceptible to hydrolytic cleavage and racemization during synthesis, maintaining exact primary sequence integrity requires rigid peptide synthesis protocols. PX1 Research utilizes solid-phase peptide synthesis (SPPS) followed by reverse-phase high-performance liquid chromatography (RP-HPLC) purification to ensure that every lot meets strict structural and purity criteria prior to distribution.
In vitro and animal models show that Selank exerts its primary neurochemical effects through indirect, allosteric modulation of the gamma-aminobutyric acid (GABA) system. Preclinical radioligand binding assays indicate that Selank does not compete directly with endogenous GABA or classic benzodiazepines at the primary ligand-binding site on GABA_A receptors. Instead, experimental data suggest Selank binds to secondary regulatory sites, altering receptor affinity and modulating chloride ion channel kinetics in rodent hippocampal and cortical tissue preparations.
In addition to GABAergic interactions, preclinical investigations demonstrate that Selank inhibits carboxypeptidase N and endopeptidase enzymes responsible for degrading endogenous enkephalins. By attenuating enkephalin breakdown, Selank prolongs the functional activity of endogenous opioid peptides involved in stress response pathways. Experimental rodent models subjected to acute emotional stress showed sustained plasma enkephalin concentrations following administration of regulatory peptides compared to vehicle controls.
Furthermore, transcriptomic and neurochemical assays reveal that Selank modulates the gene expression of neurotrophic factors. In vitro hippocampal cell cultures treated with Selank demonstrated upregulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA expression and altered monoamine turnover, specifically influencing serotonin (5-HT) and dopamine metabolite ratios in cerebral tissue.
Laboratory investigations using Selank span several distinct disciplines, including neurobiology, neuroimmunology, and molecular pharmacology. Key experimental targets include:
1. Modulation of GABAergic Neurotransmission: Investigated in rodent neuronal membranes to quantify changes in GABA receptor affinity, binding kinetics, and downstream ion flux without classical sedation markers.
2. BDNF Expression and Synaptic Plasticity: Evaluated in vitro to measure mRNA transcription changes for BDNF, TrkB receptors, and related neurotrophic signaling cascades responsible for neuronal survival and dendritic branching.
3. Enkephalin Degradation Inhibition: Analyzed in enzymatic cleavage assays to calculate inhibition constants ($K_i$) against enkephalin-degrading enzymes such as neutral endopeptidase (NEP) and aminopeptidases.
4. Neuroimmunological Interactions: Studied in isolated macrophage and lymphocyte cultures to measure cytokine expression (IL-6, TNF-alpha) and assess how tuftsin-derived sequences influence innate immune signaling.
5. Comparative Monoamine Dynamics: Measured via high-performance liquid chromatography with electrochemical detection (HPLC-ECD) in brain tissue homogenates to record changes in dopamine, norepinephrine, and 5-HIAA levels.
Researchers seeking high-purity reference material for these research pathways can buy pure Selank 10 mg vials for standardized analytical testing.
Selank is frequently studied in parallel with Semax 10 mg, another synthetic regulatory peptide derived from an endogenous peptide fragment. While Selank is derived from the immunomodulatory peptide tuftsin, Semax is an N-terminal fragment analog of adrenocorticotropic hormone (ACTH 4-10) stabilized with the same Pro-Gly-Pro C-terminal sequence.
In preclinical literature, the functional focus of these two compounds differs significantly. Selank research centers predominantly on GABAergic system modulation, enzymatic enkephalin protection, and neuroimmunological signaling. Conversely, preclinical studies on Semax focus heavily on melanocortin receptor activation, vascular endothelial growth factor (VEGF) expression, and cholinergic neurotransmission.
Researchers conducting comparative assays can review the full range of heptapeptides and regulatory analogs available across our catalog of research peptides to design precise in vitro comparative trials.
Assessing the suitability of Selank for quantitative research requires rigorous chemical characterization. Raw appearance or simple purity assertions from suppliers are insufficient for reproducible experimental setups. Laboratory buyers should require comprehensive analytical testing protocols for every batch:
Reverse-Phase HPLC (RP-HPLC): RP-HPLC separates the target peptide from synthetic side-products, truncated sequences, and deamidation products. High-grade research Selank must demonstrate a main peak purity of 99% or greater at 214 nm UV detection.
Mass Spectrometry (MS): Electrospray ionization mass spectrometry (ESI-MS) or MALDI-TOF confirms exact molecular weight matching the theoretical monoisotopic mass of Selank (751.9 g/mol), ruling out sequence errors or amino acid substitutions.
Endotoxin Testing (LAL Assay): Bacterial endotoxins (lipopolysaccharides) alter cellular responses in vitro and invalidate immunological and neurological research. Quantifying endotoxins via Chromogenic Reagent LAL assay ensures levels remain below strict threshold limits (<0.1 EU/mg).
Net Peptide Content and Residual Solvents: Lyophilized peptide preparations contain counter-ions (typically acetate or trifluoroacetate) and residual moisture. High-resolution mass spectrometry and Karl Fischer titration establish the exact peptide mass fraction per vial, enabling accurate molar concentration calculations in buffer preparations.
To ensure experimental validity and avoid batch contamination, laboratory procurement teams should benchmark suppliers against clear operational standards:
1. Sourcing and Synthesis: Verified USA-based solid-phase peptide synthesis (SPPS) using automated instrumentation.
2. Lot Traceability: Direct matching between individual vial labels, production batch numbers, and published Certificate of Analysis (COA) documents.
3. Analytical Verification: Independent third-party HPLC and MS testing performed on every production run, rather than relying on manufacturer-provided master COAs.
4. Biological Contaminant Screening: Quantified endotoxin testing and bioburden analysis performed on final lyophilized products.
5. Storage and Fulfillment Speed: Temperature-controlled storage environments ($2-8^\circ\text{C}$ or $-20^\circ\text{C}$) paired with rapid dispatch to prevent heat degradation during transit.
6. Dedicated Technical Support: Access to analytical chemists and documentation specialists capable of providing raw chromatographic data upon request.
Procurement managers and lead investigators should avoid vendors exhibiting specific operational red flags:
Generic or Reused Certificates of Analysis: Suppliers showing COAs without matching batch/lot numbers or displaying obscured testing dates are high-risk. A valid COA must reflect the specific lot delivered to your facility.
Absence of Endotoxin Data: Vendors that provide HPLC purity metrics but omit bacterial endotoxin data present severe risks for cell culture and in vitro biochemical assays sensitive to LPS contamination.
Formulation and Dosing Claims: Any supplier marketing peptides for human administration, nasal spray conversion, or clinical self-use violates compliance standards and signals non-research-grade manufacturing.
Lack of Analytical Transparency: Inability to provide full HPLC chromatograms with integration tables or mass spectrometry isotope patterns indicates inadequate quality control procedures.
Unregulated Dropshipping: Peptides shipped directly from overseas facilities without domestic quality re-verification often suffer heat damage or degradation during international transit.
Selank is supplied by PX1 Research as a sterile-filtered, lyophilized powder sealed under inert gas in vacuum-vials. To maintain structural stability and prevent hydrolytic cleavage, research protocols must adhere to proper handling procedures:
Reconstitution Protocol: Reconstitution should occur in a laminar flow hood using sterile bacteriostatic water or sterile phosphate-buffered saline (PBS, pH 7.4). The solvent should be introduced along the internal glass wall of the vial rather than sprayed directly onto the lyophilized cake to prevent shear stress on the peptide backbone.
Solubility: Selank is highly hydrophilic and dissolves rapidly in aqueous media without requiring co-solvents like DMSO.
Storage Temperature: Lyophilized powder should be stored at $-20^\circ\text{C}$ for long-term stability (up to 24 months). Reconstituted aqueous solutions should be aliquoted into single-use polypropylene tubes to avoid repeated freeze-thaw cycles and stored at $2-8^\circ\text{C}$ for short-term use (up to 14 days) or $-80^\circ\text{C}$ for extended study periods.
For additional handling specifications and technical protocols, consult the documentation available through our research library or contact our scientific staff.
When purchasing reference standards for laboratory investigation, PX1 Research provides institutional-grade consistency, rapid fulfillment, and complete analytical transparency.
What Ships: Each unit consists of a vacuum-sealed glass vial containing 10 mg of high-purity lyophilized Selank powder, labeled with a unique lot number and direct QR code link to its corresponding Certificate of Analysis.
Fulfillment & Delivery: Orders placed before 3:00 PM EST Monday through Friday ship same-day from our climate-controlled distribution facilities in California and Arizona. Fast, fully tracked domestic shipping ensures minimal ambient exposure during transit.
Quality Guarantee: Every lot is subjected to independent third-party RP-HPLC and ESI-MS testing to confirm $>99\%$ purity and exact sequence mass, along with quantitative LAL endotoxin testing.
Support & Bulk Inquiries: Our dedicated support team is available to assist research institutions with volume procurement, custom packaging requirements, and technical COA requests. To secure analytical-grade material for your laboratory, order Selank 10 mg vials directly from PX1 Research today.
What is Selank?
Selank is a synthetic regulatory heptapeptide derivative of the naturally occurring immunomodulatory peptide tuftsin, extended with a C-terminal Pro-Gly-Pro sequence. It is supplied as a research-grade compound exclusively for in vitro and preclinical laboratory investigation.
What is the primary mechanism of action of Selank in research models?
Preclinical research demonstrates that Selank functions via indirect allosteric modulation of GABA_A receptors, inhibition of enkephalin-degrading enzymes (carboxypeptidase N and endopeptidases), and upregulation of BDNF mRNA expression in cerebral tissue models.
Is Selank legal to buy for laboratory research in the US?
Yes. Selank is legal to purchase in the United States as a research chemical intended strictly for laboratory and educational use. It is not an FDA-approved drug or controlled substance, but must not be sold for human consumption or clinical application.
How do Selank and Semax differ in research application?
Selank is a tuftsin analog primarily investigated for GABAergic modulation, enkephalin protection, and neuroimmunological targets. Semax is an ACTH(4-10) analog focused on melanocortin receptor interaction, VEGF pathway expression, and cholinergic signaling.
Do you provide a lot-specific Certificate of Analysis for Selank?
Yes. Every lot of Selank distributed by PX1 Research includes a comprehensive Certificate of Analysis accessible via QR code, detailing RP-HPLC purity, electrospray ionization mass spectrometry identity, and chromogenic endotoxin assay results.
What purity level is guaranteed for PX1 Research Selank?
PX1 Research guarantees a minimum purity of 99% for Selank, as determined by reverse-phase high-performance liquid chromatography (RP-HPLC) with single-peak identity confirmed by mass spectrometry.
How fast does PX1 Research ship Selank orders?
Orders placed before 3:00 PM EST, Monday through Friday, ship same-day from our climate-controlled facilities in California and Arizona via tracked domestic shipping carriers.
How should lyophilized Selank be stored upon arrival?
Lyophilized Selank powder should be stored at -20°C in a dry environment upon receipt. Following reconstitution in sterile buffer, liquid aliquots should be kept at 2–8°C for short-term use or -80°C for long-term storage to prevent peptide degradation.
All products are sold strictly for laboratory and research use only. Not for human or veterinary use, diagnosis, treatment or consumption. Statements have not been evaluated by the FDA.