Geef 15% korting, verdien 10% terug op elke bestelling die zij plaatsen.
Verbinding van onderzoekskwaliteit. Uitsluitend voor laboratoriumgebruik. Niet bedoeld voor gebruik bij mensen of dieren, inname of injectie. Er worden geen medische claims gemaakt of geïmpliceerd.
Levering aan EU binnen 11-14 werkdagen
Gratis verzending vanaf €200 · geen douanepapieren (EU) · via EU carrier network
Gratis verzending bij bestellingen boven €200
Research-grade Triptorelin Acetate. 99.3% avg purity, HPLC & MS verified. Lyophilized powder in sealed glass vial. For laboratory research use only. Not for human consumption.
| Aantal | Stukprijs | Totaal | Besparing |
|---|---|---|---|
| 1 unit | € 29,99 | € 29,99 | -- |
| 3+ | € 28,49 | € 85,47 | 5% korting |
| 5+Meest gekozen | € 26,99 | € 134,95 | 10% korting |
| 10+ | € 25,49 | € 254,92 | 15% korting |
Belangrijke mededeling
Dit product is uitsluitend bestemd voor laboratorium- en onderzoeksgebruik. Niet voor gebruik bij mensen of dieren. Door dit product te kopen, bevestigt u dat het uitsluitend zal worden gebruikt voor in-vitro onderzoeksdoeleinden.
Reconstitutie vereist
Dit peptide wordt gelyofiliseerd verzonden (droog poeder) en vereist bacteriostatisch water om te reconstitueren vóór gebruik. BAC-water wordt apart verkocht.
99,3% gemiddelde HPLC-zuiverheid, geverifieerd door onafhankelijke externe tests
Janoshik-rapport gepubliceerd zodra beschikbaar
Verzending binnen 24 uur, EU-brede verzending vanaf €4,99
Leveranciersbatchspecificatie op elk product; onafhankelijk Janoshik-rapport op geselecteerde loten
Triptorelin is a GnRH agonist analogue -- a synthetic decapeptide with modifications at positions 6 and 10 of the native GnRH sequence that dramatically increase potency and half-life compared to endogenous GnRH. It is FDA- and EMA-approved for prostate cancer, endometriosis, and central precocious puberty under various brand names. Like all long-acting GnRH agonists, it produces an initial "flare" of LH and FSH (and consequently sex steroids) followed by receptor desensitization and profound gonadotropin suppression -- reducing circulating testosterone in men to castrate levels. Each vial contains 2mg.
The mechanism of action is counterintuitive until the receptor biology is understood. GnRH receptors respond to pulsatile stimulation; continuous high-level agonism from a long-acting analogue causes receptor downregulation and uncoupling from intracellular signaling. After 2-4 weeks of continuous exposure, LH and FSH secretion drops dramatically, and consequently so do testosterone and estradiol. This chemical castration is medically equivalent to surgical castration for testosterone-sensitive conditions.
For research applications, triptorelin is used to study GnRH receptor pharmacology, model hypogonadism (chemical castration models), investigate hormone-sensitive tissue biology in the absence of sex steroids, and as a positive control for GnRH agonist effects. The initial flare followed by suppression pattern also makes it useful for timing-controlled endocrine studies.
| Parameter | Value |
|---|---|
| Compound | Triptorelin acetate (GnRH agonist analogue) |
| Amount per Vial | 2mg |
| Purity | 99.3% avg (HPLC verified) |
| Format | Lyophilized powder |
| Reconstitution | Sterile water or saline |
| Storage | -20°C; 2-8°C after reconstitution |
Store at -20°C before reconstitution. Refrigerate at 2-8°C after reconstitution and use within 14 days. Protect from light.
This is the paradox of GnRH agonist pharmacology. The pituitary GnRH receptor requires pulsatile stimulation to maintain LH and FSH secretion. When triptorelin provides continuous (rather than pulsatile) stimulation due to its long half-life, GnRH receptors become desensitized -- they downregulate and uncouple from signaling. After 2-4 weeks, LH and FSH secretion drops to very low levels, testosterone follows, and the result is chemical castration. The initial "flare" (a brief period of increased LH/FSH/testosterone before desensitization) is clinically important in prostate cancer because it can temporarily worsen symptoms before suppression begins.
In animal research, triptorelin (or other long-acting GnRH agonists) administered at sufficient doses produces reliable hypogonadism -- very low testosterone -- without surgical castration. This "chemical castration" model is useful for studying androgen-dependent processes, testing testosterone replacement or alternative therapies, and investigating testosterone's role in specific physiological systems. After cessation of triptorelin treatment, endogenous testosterone production recovers (unlike surgical castration), making chemical castration models reversible -- useful for before/after study designs.
All three are GnRH agonist analogues with the same fundamental mechanism of GnRH receptor desensitization and gonadotropin suppression. They differ primarily in modification sites, formulation, and half-life. Triptorelin is available as short-acting (daily injection) and long-acting (monthly/3-monthly depot) formulations. Leuprolide is similar with multiple depot options. Goserelin is formulated exclusively as a subcutaneous implant. For research, the short-acting daily-injection form of triptorelin or leuprolide allows better dose control than depot formulations, where the release kinetics add variability.
Triptorelin is supplied for laboratory research use only. Not approved for general human use outside of licensed therapeutic indications. Handle in compliance with institutional biosafety guidelines.
Triptorelin is a GnRH agonist analogue -- a synthetic decapeptide with modifications at positions 6 and 10 of the native GnRH sequence that dramatically increase potency and half-life compared to endogenous GnRH. It is FDA- and EMA-approved for prostate cancer, endometriosis, and central precocious puberty under various brand names. Like all long-acting GnRH agonists, it produces an initial "flare" of LH and FSH (and consequently sex steroids) followed by receptor desensitization and profound gonadotropin suppression -- reducing circulating testosterone in men to castrate levels. Each vial contains 2mg.
The mechanism of action is counterintuitive until the receptor biology is understood. GnRH receptors respond to pulsatile stimulation; continuous high-level agonism from a long-acting analogue causes receptor downregulation and uncoupling from intracellular signaling. After 2-4 weeks of continuous exposure, LH and FSH secretion drops dramatically, and consequently so do testosterone and estradiol. This chemical castration is medically equivalent to surgical castration for testosterone-sensitive conditions.
For research applications, triptorelin is used to study GnRH receptor pharmacology, model hypogonadism (chemical castration models), investigate hormone-sensitive tissue biology in the absence of sex steroids, and as a positive control for GnRH agonist effects. The initial flare followed by suppression pattern also makes it useful for timing-controlled endocrine studies.
| Parameter | Value |
|---|---|
| Compound | Triptorelin acetate (GnRH agonist analogue) |
| Amount per Vial | 2mg |
| Purity | 99.3% avg (HPLC verified) |
| Format | Lyophilized powder |
| Reconstitution | Sterile water or saline |
| Storage | -20°C; 2-8°C after reconstitution |
Store at -20°C before reconstitution. Refrigerate at 2-8°C after reconstitution and use within 14 days. Protect from light.
This is the paradox of GnRH agonist pharmacology. The pituitary GnRH receptor requires pulsatile stimulation to maintain LH and FSH secretion. When triptorelin provides continuous (rather than pulsatile) stimulation due to its long half-life, GnRH receptors become desensitized -- they downregulate and uncouple from signaling. After 2-4 weeks, LH and FSH secretion drops to very low levels, testosterone follows, and the result is chemical castration. The initial "flare" (a brief period of increased LH/FSH/testosterone before desensitization) is clinically important in prostate cancer because it can temporarily worsen symptoms before suppression begins.
In animal research, triptorelin (or other long-acting GnRH agonists) administered at sufficient doses produces reliable hypogonadism -- very low testosterone -- without surgical castration. This "chemical castration" model is useful for studying androgen-dependent processes, testing testosterone replacement or alternative therapies, and investigating testosterone's role in specific physiological systems. After cessation of triptorelin treatment, endogenous testosterone production recovers (unlike surgical castration), making chemical castration models reversible -- useful for before/after study designs.
All three are GnRH agonist analogues with the same fundamental mechanism of GnRH receptor desensitization and gonadotropin suppression. They differ primarily in modification sites, formulation, and half-life. Triptorelin is available as short-acting (daily injection) and long-acting (monthly/3-monthly depot) formulations. Leuprolide is similar with multiple depot options. Goserelin is formulated exclusively as a subcutaneous implant. For research, the short-acting daily-injection form of triptorelin or leuprolide allows better dose control than depot formulations, where the release kinetics add variability.
Triptorelin is supplied for laboratory research use only. Not approved for general human use outside of licensed therapeutic indications. Handle in compliance with institutional biosafety guidelines.
Vertrouwen van onderzoekers
Wie test dit eigenlijk?
Geselecteerde partijen worden onafhankelijk geverifieerd door Janoshik Analytical (Tsjechië) en gepubliceerd op het openbare Janoshik-portaal. Andere partijen worden geleverd met de batchspecificatie van de leverancier. Zie /coa voor de gepubliceerde muur.
COA's bekijken →Wat als ik de verkeerde batch krijg?
Elk fleslabel draagt een lotnummer dat verwijst naar een specifiek Certificate of Analysis. Als een batch niet aan de specificatie voldoet, verzenden wij hem niet — punt uit.
COA's bekijken →Vanwaar wordt het verzonden?
Roemenië (EU). Wij zijn CERTALAB SRL, CUI 54169956, btw-geregistreerd. Sameday voor Roemenië, GLS voor de meeste EU-bestemmingen, TCE Worldwide voor de overige grensoverschrijdende EU- en niet-EU-markten (VK, Zwitserland, Noorwegen, IJsland, Israël, Servië). Bezorging 1–15 werkdagen afhankelijk van de bestemming — exacte termijn getoond bij het afrekenen.
Verzendgegevens →Wat als er een probleem is?
U heeft een herroepingsrecht van 14 dagen op grond van OUG 34/2014 (Roemeens/EU-consumentenrecht), met mogelijkheid tot escalatie via ANPC/ODR. Neem contact met ons op via support@certapeptides.com.
Retourbeleid →Dit product is uitsluitend bedoeld voor wetenschappelijk onderzoek en ontwikkeling. Het is een chemische stof die niet mag worden gebruikt als geneesmiddel, medicijn, werkzame stof of ingrediënt in enig product bedoeld voor menselijke of dierlijke consumptie. Onderzoekers dienen deze verbinding te hanteren in overeenstemming met hun institutionele bioveiligheidsrichtlijnen. Gebruik deze uitsluitend in goed uitgeruste laboratoriumomgevingen met geschikte persoonlijke beschermingsmiddelen.