Kisspeptin-10
10MG
Kisspeptin-10 stimulates reproductive hormone signaling through GnRH pathways involved in hormonal regulation and fertility.
In stock | ≥99% catalog purity
Description
Product specification
Analytical Profile
Catalog data is presented for material identification and laboratory planning. Batch-specific documentation governs the supplied vial.
| RESEARCH NAME | Kisspeptin-10 · KP-10 |
| FORMAT | Lyophilised powder · 10 mg vial |
| MOLECULAR FORMULA | C63H83N17O14 |
| MOLECULAR MASS | 1302.4 g/mol |
| CAS REGISTRY | 374675-21-5 |
| ANALYTICAL IDENTITY | HPLC + LC–MS |
| CATALOG CONDITION | Sealed · dry · light-protected · −20°C |
PROTOCOL LITERACY
Reconstitution Sequence
This source-derived sequence assumes a 10 mg vial and a final reference volume of 1.0 mL. The supplied product documentation remains the controlling instruction.
01
02
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04
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UNRECONSTITUTED MATERIAL
-20°C
Keep frozen, dry, sealed, and protected from direct light. Minimise moisture exposure because NAD+ powder is hygroscopic.
After reconstitution
2-8°C
Handling principle
ONE THAW
Avoid repeated freeze–thaw cycles. The prepared solution should remain clear and colourless; discard it if cloudiness, discolouration, or precipitate develops.
PROTOCOL LITERACY
SS-31 DOSAGE CHART
A designed reference covering concentration, weekly schedule models, reconstitution, supply planning, storage, mechanism, study observations, and administration context. It is educational material—not an individualized regimen.
VIAL CONTENT
1.0 MG
+
REFERENCE DILUENT
1.0 MG
=
STOCK CONCENTRATION
1.0 MG/ML
U-100 SCALE
1 Unit = 0.01 ml 100 mcg
01
GRADUAL 8MG MODEL
02
12 MG TRIAL CONTEXT
EDUCATIONAL REFERENCE
GRADUAL DAILY MODEL
| STUDY INTERVAL | STAGE | WEEKLY DOSE | U-100 REFERENCE | SOLUTION VOLUME |
|---|---|---|---|---|
01
WEEKS 1 | INITIATION | 10 MG | 60 UNITS | 0.30 ML |
01
REFERENCE ASSUMPTIONS
Every unit and volume value shown assumes a 10 mg vial prepared to a total reference volume of 1.0 mL.
02
MATERIAL BOUNDARY
This table does not provide preparation or administration instructions.
03
PROTOCOL CONTROL
Trial documentation and qualified clinical oversight—not this chart—must govern all dosing decisions.
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