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SLU-PP-332 – Potent ERRα Agonist for Metabolic & Performance Research
1 SLU-PP-332 5mg
1 DMSO Solution 60ml
SLU-PP-332 is a novel, selective Estrogen-Related Receptor Alpha (ERRα) agonist that directly enhances mitochondrial biogenesis and energy expenditure. Ideal for studying:
✔ Metabolic disease & obesity mechanisms
✔ Exercise endurance & muscle remodeling
✔ Neuroprotection & cognitive function
✔ Cellular energy & anti-aging pathways
Reconstitution Guidance: SLU-PP-332 is typically soluble in DMSO for creating a concentrated stock solution (e.g., 10-50 mM), which can then be further diluted in saline or cell culture media for final dosing. The final concentration of DMSO in any in vitro or in vivo application should not exceed 1% to avoid cytotoxicity.
Key Features:
≥98% HPLC/MS verified purity
Direct ERRα targeting for precise research
Lyophilized powder for optimal stability
Research use only (not for human/veterinary use)
HPLC Test Results: https://janoshik.com/tests/75909-SLUPP332_A3PF2VC6JB1F
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Disclaimer: This product is for laboratory research purposes only. Not for human or animal consumption.
| select | With DMSO, Without DMSO |
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The SLU-PP-332 5mg With/Without DMSO 60mlERRα agonist research compound for metabolic studies is a potent and selective tool for investigating cellular energy and mitochondrial biogenesis. Because this novel small molecule directly activates the Estrogen-Related Receptor Alpha (ERRα), it functions as a master transcriptional regulator. Furthermore, researchers utilize this compound to explore pathways involving energy expenditure and adaptive thermogenesis in advanced laboratory models.
The profound effects of the SLU-PP-332 ERRα agonist research compound for metabolic studies are mediated through its highly specific interaction with nuclear receptors. By “switching on” ERRα, the compound triggers several critical downstream effects:
Transcriptional Activation: It binds to response elements to upregulate PGC-1α, the master regulator of mitochondrial creation.
Mitochondrial Biogenesis: The compound forces a robust increase in the density and oxidative capacity of existing mitochondria.
Substrate Utilization: It promotes a metabolic preference for fatty acids. Consequently, this helps researchers study glucose sparing and improved insulin sensitivity.
When scientists apply the SLU-PP-332 ERRα agonist research compound for metabolic studies, they observe striking results across various preclinical domains. Specifically, evidence-based studies highlight the following:
Metabolic Disease & Obesity: Treatment in diet-induced obese models reveals marked improvements in glucose tolerance. Moreover, it promotes fat mass reduction without decreasing caloric intake.
Exercise Performance: Rodents exhibit a staggering increase in running endurance, often exceeding 70% longer than control groups. This occurs because the compound transforms skeletal muscle into a fatigue-resistant phenotype.
Neuroprotection: Since neurons are highly energy-dependent, SLU-PP-332 provides the necessary ATP to maintain synaptic function and resilience against oxidative stress.
To achieve consistent experimental results, you must follow established guidelines for the SLU-PP-332 ERRα agonist research compound for metabolic studies. The table below outlines standard laboratory protocols:
| Research Model | Suggested Dosage | Administration | Key Parameters |
| In Vitro | 0.1 – 5.0 µM | Dissolved in DMSO | OCR, Gene Expression |
| Mouse Models | 5 – 15 mg/kg | IP Injection/Gavage | Endurance, Glucose Tolerance |
| Rat Models | 3 – 10 mg/kg | IP Injection/Gavage | Muscle Fiber Typing |
At EliteBiogenix, we provide high-purity SLU-PP-332 ERRα agonist research compound for metabolic studies ($\ge$98%) verified by HPLC. For proper handling, dissolve the lyophilized powder in DMSO to create a concentrated stock solution. Subsequently, you may dilute this in saline for final dosing. To maintain the highest stability, store the original vial at -20°C and protect it from light and moisture.
Research Grade CJC-1295 No DAC (Modified GRF 1-29) – 5mg
This high-purity synthetic GHRH analog is designed for precise endocrine research. CJC-1295 No DAC lacks the Drug Affinity Complex, allowing researchers to study pulsatile growth hormone release patterns in pituitary cell cultures without sustained elevation.
Primary Research Applications:
Pituitary Somatotroph Function & GH Secretion Studies
GHRH Receptor Signaling & cAMP Pathway Analysis
Comparative Research with DAC-Containing Analogs
Pulsatile GH Release & Metabolic Modeling
Intended for laboratory use only by qualified researchers. This product is strictly not for human or veterinary consumption.
Sequence: Tetra-substituted GRF 1-29 Purity: ≥98% (HPLC Verified) Form: 5mg lyophilized powder Storage: Store at -20°C or below, desiccated and protected from light.
This premium synthetic 28-amino acid peptide is designed for advanced immunological and anti-aging research. Since this compound is highly pure ($\ge$99%), it remains a critical tool for studying complex biological pathways.
Researchers primarily use this immunomodulatory compound to investigate various cellular processes. Specifically, it is essential for studying:
T-cell Dynamics: Analyzing maturation, differentiation, and overall function.
Immunosenescence: Investigating age-related immune decline.
Inflammatory Pathways: Evaluating cytokine regulation and anti-inflammatory responses.
Oncological Models: Testing adjunct therapies within specialized cancer research.
Infection Response: Modulating responses in sepsis and viral infection models.
This peptide is perfectly suited for several specific research applications. For instance, it is often utilized in:
Immunodeficiency and reconstitution studies.
Anti-aging and "inflammaging" research projects.
Innovative cancer immunotherapy combinations.
Vaccine adjuvant response protocols.
Note on Reconstitution: This peptide is highly acidic. Consequently, it requires .1-1% Acetic Acid for proper reconstitution.
Please be aware that cloudiness or clumping may occur because the molecules are "intrinsically disordered." Furthermore, this physical characteristic is a natural property of the molecule.
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