Dual-Peptide Research Blend
Selank + Semax 20 mg Research Peptide Blend
A defined dual-component research formulation containing
Selank 10 mg and Semax 10 mg in a single 20 mg lyophilized
research vial. The formulation combines two distinct synthetic
heptapeptides for controlled multi-component peptide research.
Selank 10 mg
Semax 10 mg
20 mg Total
1:1 Blend
Dual Heptapeptide
Batch Traceability
Research Use Only
Not for human or veterinary use, administration, ingestion,
injection, compounding, diagnostic, therapeutic, clinical,
or personal use.
01
Blend Profile
Selank + Semax Research Material
The Selank + Semax 20 mg blend is a defined two-component
research formulation containing equal quantities of two
structurally distinct synthetic heptapeptides.
Selank is structurally related to the tuftsin peptide sequence,
while Semax is structurally associated with an ACTH-derived
peptide fragment. Both contain seven amino-acid residues but
maintain separate molecular identities within the blend.
Royal Peptides supplies this formulation exclusively as a
laboratory research material for controlled analytical and
experimental investigation.
02
Defined Composition
10 mg Selank + 10 mg Semax
The 20 mg vial contains a defined 1:1 composition by labeled
peptide mass, providing equal quantities of Selank and Semax
within a single research formulation.
Component 01
Selank
10 mg
Synthetic heptapeptide structurally derived from a
tuftsin-related peptide sequence.
Component 02
Semax
10 mg
Synthetic heptapeptide structurally associated with an
ACTH-derived peptide fragment.
TOTAL LABELED PEPTIDE CONTENT •
20 mg
03
Component Identification
Two Distinct Heptapeptides
Selank
10 mg
Heptapeptide component
Selank Sequence
TKPRPGP
Thr-Lys-Pro-Arg-Pro-Gly-Pro
Semax
10 mg
Heptapeptide component
Semax Sequence
MEHFPGP
Met-Glu-His-Phe-Pro-Gly-Pro
Selank Component
Selank provides one defined seven-residue peptide sequence
within the formulation and retains its individual compound
identity for analytical research.
Semax Component
Semax provides a separate seven-residue peptide sequence
within the formulation and remains analytically distinct
from Selank.
Shared PGP Terminus
Both peptide sequences contain a Pro-Gly-Pro sequence at
their C-terminal region, providing a useful structural
feature for comparative laboratory investigation.
Defined 1:1 Composition
Equal labeled quantities provide a controlled dual-component
material for experiments requiring a predefined Selank-to-Semax
ratio.
04
Scientific Context
Controlled Multi-Component Research
Selank and Semax have individually appeared in experimental
literature involving peptide-associated molecular and
neurobiological systems. A blended material can support controlled
research designs where both defined peptide components are evaluated
within the same experimental system.
Comparative Peptide Research
Researchers may investigate structural or analytical
similarities and differences between the two defined
heptapeptide components.
Molecular Signaling Models
Controlled experimental systems may examine measurable
molecular variables associated with peptide signaling
pathways.
Multi-Component Analysis
The formulation provides a defined dual-component material
for analytical methods designed to distinguish or quantify
multiple peptide constituents.
Structure-Function Research
The distinct parent sequences together with their shared
Pro-Gly-Pro terminal motif provide structural variables for
controlled comparative investigation.
05
Analytical Documentation
Batch-Specific Research Information
Laboratory evaluation should rely on analytical documentation
corresponding to the specific production lot received. For a
multi-component formulation, researchers should distinguish
between total labeled material quantity and the identity or
measured content of each individual peptide component.
- Selank component identification
- Semax component identification
- Production lot or batch reference
- Declared 10 mg + 10 mg composition
- Analytical testing information
- Purity information where applicable
- Testing methodology where documented
- Batch-specific documentation where available
06
Traceability
Research Records & Batch Control
Appropriate research records should connect experimental
observations to the specific Selank + Semax production lot
incorporated into the laboratory workflow.
Blend Identification
Record the formulation name, individual component quantities,
total labeled quantity, production lot, date received, and
applicable internal laboratory identifier.
Analytical Records
Preserve applicable analytical documentation, experimental
observations, results, material-control records, and other
records associated with the specific research lot.
07
Laboratory Protocol
Handling & Storage
Selank + Semax research material should be handled using
appropriate laboratory procedures intended to preserve material
identity, minimize contamination, and maintain experimental
traceability.
Laboratory Handling
Maintain clear identification of the dual-component material
throughout receipt, storage, analytical preparation, and
experimental workflows.
Storage & Documentation
Follow storage information associated with the applicable
product label and batch documentation rather than relying on
generalized storage claims.
08
Important Restrictions
Research Use Limitations
Royal Peptides Selank + Semax 20 mg is supplied exclusively as a
laboratory research material. It is not offered or represented as
a medicine, pharmaceutical preparation, dietary supplement, food,
cosmetic, or consumer health product.
- Not for human administration
- Not for veterinary administration
- Not for ingestion or injection
- Not for personal experimentation
- Not for pharmaceutical compounding
- Not for pharmacy preparation
- Not for diagnostic or therapeutic use
- Not for clinical use
09
Research FAQ
Selank + Semax Blend Questions
What is in the Selank + Semax 20 mg blend?
The formulation contains 10 mg of Selank and 10 mg of
Semax, providing 20 mg total labeled peptide material in
a 1:1 ratio.
Is Selank + Semax a single peptide?
No. It is a blend containing two separate synthetic
heptapeptides. Selank and Semax retain distinct amino-acid
sequences and molecular identities.
What is the Selank sequence?
Selank is commonly identified as
Thr-Lys-Pro-Arg-Pro-Gly-Pro, abbreviated TKPRPGP.
What is the Semax sequence?
Semax is commonly identified as
Met-Glu-His-Phe-Pro-Gly-Pro, abbreviated MEHFPGP.
How are Selank and Semax structurally different?
Selank is structurally related to a tuftsin-derived peptide
sequence, while Semax is associated with an ACTH-derived
peptide fragment. They are distinct compounds despite both
being seven-residue peptides.
What do Selank and Semax have in common?
Both are synthetic heptapeptides and both contain a
Pro-Gly-Pro sequence at their C-terminal region. Their
remaining sequences and structural origins differ.
Is the blend intended for human use?
No. Royal Peptides supplies this formulation strictly for
laboratory research. It is not intended for human or
veterinary administration.
Does Royal Peptides provide dosing instructions?
No. Royal Peptides does not provide dosing, administration,
injection, prescribing, treatment, or personal-use
instructions for this research material.
Is analytical documentation available?
Batch-specific analytical documentation may be available
for the applicable production lot. Researchers should review
documentation corresponding to the specific material received.
Research Use Only
Dual-Component Laboratory Research Material
Selank + Semax 20 mg is supplied for laboratory research use only.
Not for human or veterinary use. Not intended for administration,
ingestion, injection, personal experimentation, pharmaceutical
compounding, pharmacy preparation, diagnostic use, therapeutic use,
or clinical use. Nothing on this page constitutes medical advice or
represents this research material as intended to diagnose, treat,
cure, mitigate, or prevent any disease or medical condition.