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HMG (75iu)

$130.00

Product Usage DisclaimerΒ 

This material is suppliedΒ exclusively as a laboratory research chemicalΒ forΒ in vitro scientific study. All descriptions and are providedΒ for informational and educational purposes only.

This compound isΒ not approvedΒ for human or animal consumption, injection, ingestion, inhalation, topical use, or any other biological application. It must be handled only by qualified, trained personnel in a properly equipped laboratory.

This product isΒ notΒ a drug, supplement, food, cosmetic, or therapeutic agent, and it may not be rebranded, repackaged, or marketed as any such item.Β Misuse, mislabeling, or unauthorized application is strictly prohibited.

Nothing on this website constitutes medical advice, professional guidance, or a recommendation of use.

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Description

HMG – Advanced Biochemical Mechanism Profile

(Human Menopausal Gonadotropin; FSH/LH Glycoprotein Hormone Blend)

HMG is a purified gonadotropin complex containing biologically active Follicle-Stimulating Hormone (FSH) and Luteinizing Hormone (LH). Both components are heterodimeric glycoproteins that activate distinct but related G-protein–coupled receptors:

  • FSH β†’ FSHR (Follicle-Stimulating Hormone Receptor)

  • LH β†’ LHCGR (LH/Choriogonadotropin Receptor)

Both receptors are Gs-coupled GPCRs, driving adenylate cyclase β†’ ↑ cAMP β†’ PKA β†’ CREB-regulated transcription.


βœ… 1. FSH Signaling

Receptor Target

FSHR (Class A GPCR) β€” expressed in ovarian granulosa and testicular Sertoli cell models

Primary intracellular cascade

  1. FSH β†’ FSHR

  2. Gs activation

  3. Adenylate cyclase β†’ ↑ cAMP

  4. PKA phosphorylation

  5. CREB nuclear translocation

  6. Transcription of steroidogenic and gametogenic genes

Common downstream biochemical outputs

  • ↑ Aromatase activity (CYP19A1)

  • ↑ cAMP-responsive genes in Sertoli and granulosa cell lines

Gene targets frequently measured

Functional Area Genes
Steroidogenesis CYP19A1, CYP11A1, StAR
Gametogenesis FSHR, AMH, INHBA/INHBB
Sertoli cell support GDNF, SOX9

βœ… 2. LH Signaling

Receptor Target

LHCGR (Gs-coupled GPCR) β€” expressed in Leydig and theca cell models

Primary cascade

  1. LH β†’ LHCGR

  2. Gs β†’ Adenylate cyclase

  3. ↑ cAMP

  4. ↑ PKA activity

  5. Phosphorylation of StAR (Steroidogenic Acute Regulatory protein)

  6. Cholesterol import to mitochondria β†’ steroid formation

Steroidogenic enzymes upregulated

  • CYP11A1 (cholesterol β†’ pregnenolone)

  • HSD3B1

  • CYP17A1

  • CYP19A1 (aromatase)

Gene-level markers

Category Genes
Steroid hormones StAR, CYP11A1, HSD3B1, CYP17A1, CYP19A1
Receptor regulation LHCGR
Anti-apoptotic pathways BCL2, MCL1

βœ… 3. Shared Signaling Mechanisms (FSH + LH)

  • cAMP accumulation

  • PKA activation

  • CREB phosphorylation

  • Increased transcription at cAMP-response element (CRE) promoters

  • Upregulation of steroid biosynthesis pathways

  • Modulation of mitochondrial cholesterol transport


βœ… 4. Secondary Pathways

Although cAMP/PKA is dominant, research models show additional signaling:

PI3K β†’ Akt

  • Promotes cell survival and mitochondrial stability

  • Regulates anti-apoptotic gene transcription (BCL2, BAX ratio)

ERK1/2 MAPK

  • Ras β†’ Raf β†’ MEK1/2 β†’ ERK1/2

  • Drives growth and differentiation of gonadal cells

Ca²⁺-dependent signaling

  • PKA-modulated Ca²⁺ channel function supports vesicular secretion


βœ… 5. Key Enzymes & Proteins in HMG Signaling

Component Function
Adenylate cyclase cAMP synthesis
PKA Phosphorylates steroidogenic proteins
CREB Transcriptional regulation
StAR Mitochondrial cholesterol transport
CYP11A1 / CYP17A1 / CYP19A1 Steroid metabolism enzymes
HSD3B1 Progesterone & androgen pathway

βœ… 6. Frequently Monitored Gene Panels in Studies

  • StAR, CYP11A1, CYP19A1, CYP17A1 (steroidogenesis)

  • FSHR, LHCGR (receptor expression feedback)

  • AMH, INHBA/INHBB (granulosa cell markers)

  • GDNF, SOX9 (Sertoli cell signaling)

  • BCL2/MCL1 (anti-apoptotic response)


Research-Only Use Classification

HMG is supplied exclusively for controlled in-vitro laboratory research.
It is not approved for human or animal administration, ingestion, injection, or therapeutic/diagnostic use.

Additional information

Weight N/A
Size

75iu