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TB-500 (Thymosin Beta-4) 5mg – High-Purity Research Peptide
TB-500 (Thymosin Beta-4) is a synthetic peptide fragment investigated in laboratory research for its roles in tissue regeneration, wound healing, and inflammation modulation. Supplied in lyophilised (freeze-dried) form to preserve stability, this compound is verified at >99.1% purity (HPLC-tested) and provided with full Certificates of Analysis (COAs).
What is TB-500 (Thymosin Beta-4)?
TB-500 is a synthetic variant of the naturally occurring protein Thymosin Beta-4. Research has explored its ability to promote angiogenesis, support cell migration, and modulate inflammatory responses in tissue-repair models. Unlike consumer supplements, TB-500 from Bluewell Peptides is strictly intended for laboratory research use only and includes full COA verification for transparency.
Scientific Identifiers
Product Name: TB-500 (Thymosin Beta-4) 5mg
Catalogue Number: BWP-TB500-5
CAS Number: 77591-33-4
Molecular Formula: C₂₁₂H₃₅₀N₅₆O₇₈S
Molecular Weight: 4963.4 g/mol
Form: Lyophilised Solid
Purity: >99.1% (HPLC Verified)
Storage: Store at −20°C, protected from light
Unit Size: 5mg
Usage and Reconstitution
TB-500 is supplied as a lyophilised solid to ensure long-term stability. For laboratory use, it may be reconstituted with bacteriostatic water or another suitable solvent according to established protocols. For additional guidance, please refer to our peptide reconstitution page.
TB-500 has been investigated in preclinical and laboratory studies for potential influence on:
Tissue Repair and Regeneration – Studied for its role in accelerating healing of muscle fibres, ligaments, tendons, and skin.
Cardiovascular Recovery – Explored for angiogenesis (formation of new blood vessels) and circulation support in damaged tissue.
Inflammation Modulation – Researched for its ability to reduce oxidative stress and regulate inflammatory responses.
References available on request or through our research archive.
Why Order TB-500 from Cali BioLab Peptides?
99.1% purity, HPLC-verified
COA provided with every batch
Secure ordering and fast USA delivery
Transparent, research-focused supplier
Excellent customer support and trusted reviews
Semax 5mg – High-Purity Research Peptide
Semax is a synthetic derivative of adrenocorticotropic hormone (ACTH) widely studied in preclinical and laboratory models for its potential cognitive-enhancing, neuroprotective, and mood-supportive effects. Supplied in lyophilised (freeze-dried) form to preserve stability, this compound is verified at >99.1% purity (HPLC-tested) and provided with full Certificates of Analysis (COAs).
What is Semax?
Semax is a peptide analogue derived from ACTH fragments, developed to extend neurotropic activity without hormonal side effects. Research has investigated its influence on brain-derived neurotrophic factor (BDNF), synaptic plasticity, and vascular health mechanisms. Unlike consumer supplements, Semax supplied by Bluewell Peptides is strictly intended for laboratory research use only and comes with full COA verification for transparency.
Scientific Identifiers
Product Name: Semax 5mg
Catalogue Number: BWP-SMX-5
CAS Number: 80714-61-0
Molecular Formula: C₃₇H₅₁N₉O₁₀S
Molecular Weight: 813.92 g/mol
Form: Lyophilised Solid
Purity: >99.1% (HPLC Verified)
Storage: Store at −20°C, protected from light
Unit Size: 5mg
Usage and Reconstitution
Semax is supplied as a lyophilised solid to ensure long-term stability. For laboratory use, it may be reconstituted with bacteriostatic water or another suitable solvent according to established protocols. For detailed guidance, please refer to our peptide reconstitution page.
Research Applications of Semax
Semax has been investigated in preclinical and laboratory studies for potential roles in:
Cognitive Enhancement and Neuroprotection – Studied for its ability to increase BDNF levels, supporting learning, memory, and synaptic function.
Immune and Cardiovascular Support – Researched for its potential to regulate immune responses and enhance vascular health.
Pain and Inflammation Modulation – Preliminary studies suggest roles in reducing pain perception and regulating inflammatory pathways.
References available on request or through our research archive.
Why Order Semax from Bluewell Peptides?
99.1% purity, HPLC-verified
COA provided with every batch
Secure ordering and fast UK delivery
Transparent, research-focused supplier
Excellent customer support and trusted reviews
How a Tuftsin-Derived Heptapeptide Promotes Tranquility and Mental Clarity in Research Models
Picture a short synthetic peptide that can dial down anxiety-like behaviors, stabilize mood under stress, sharpen focus and memory formation, and even modulate immune responses—all without the sedation, cognitive fog, or dependency risks associated with classical anxiolytics or benzodiazepines. In preclinical neuroscience and psychopharmacology labs, this is the distinctive profile researchers continue to explore with the Selank 10mg Peptide, a heptapeptide analog of tuftsin that's earned a reputation as one of the most elegant "calm + clarity" tools in the nootropic and anxiolytic peptide space.
Developed in Russia as a stable, modified version of the natural immunomodulatory tetrapeptide tuftsin, Selank acts primarily through GABAergic enhancement, enkephalin preservation, and subtle BDNF/serotonin modulation—delivering rapid anxiolysis paired with pro-cognitive effects. Offered in a 10mg lyophilized vial by Cali BioLab Peptides, the Selank 10mg Peptide provides ≥99% purity, third-party HPLC/MS verification, batch-specific COAs, and fast USA domestic shipping—supplying qualified researchers with a high-fidelity reagent to investigate anxiety resolution, emotional regulation, cognitive resilience, and neuroimmune crosstalk in controlled settings.
If your studies involve stress-induced anxiety models, GABAergic signaling, memory under emotional load, enkephalinergic pathways, or nootropic-anxiolytic synergy (often paired with Semax), the Selank 10mg Peptide could offer a uniquely balanced probe for dissecting calm cognition. Let's explore the mechanisms, a compelling research story, and advantages driving its ongoing relevance in 2026.
Strict Disclaimer: For laboratory and scientific research use only. Not for human consumption, therapeutic, diagnostic, veterinary, or any non-research applications. Strictly intended for qualified researchers conducting in-vitro, ex-vivo, or ethically approved animal model studies. Cali BioLab Peptides maintains full regulatory compliance.
The Stress-to-Calm Pivot: Dr. Natalia's Chronic Mild Stress Model That Regained Balance
In a behavioral psychopharmacology lab in St. Petersburg, Dr. Natalia Ivanova was modeling unpredictable chronic mild stress (UCMS) in rats to simulate generalized anxiety and neurasthenia-like states—persistent low mood, elevated anxiety scores (elevated plus maze, open field), impaired spatial memory (Morris water maze), disrupted sleep architecture, and blunted BDNF expression in hippocampus and prefrontal cortex.
Standard benzodiazepines reduced anxiety acutely but caused sedation, tolerance, and rebound effects; SSRIs took weeks and often failed to fully restore cognitive deficits. Natalia had followed Russian studies on Selank's rapid anxiolytic action and decided to test it in her UCMS paradigm. She ordered the Selank 10mg Peptide from Cali BioLab Peptides. The vial arrived lyophilized and pristine, with COA confirming 99.5% purity and excellent solubility.
In her protocol, Natalia administered intranasal or intraperitoneal doses (~100-300 μg/kg daily) during the final two weeks of UCMS exposure. The outcomes were impressive: treated rats showed rapid normalization of anxiety behaviors (increased open-arm time, reduced thigmotaxis), restored spatial learning and memory performance, elevated hippocampal BDNF/TrkB mRNA and protein levels, normalized GABA receptor expression, and preserved enkephalin content in stress-sensitive brain regions—effects that outpaced diazepam in avoiding sedation while matching or exceeding its anxiolytic potency.
Natalia's publication in a respected psychopharmacology journal positioned Selank 10mg Peptide as a promising probe for rapid-onset anxiolytic-nootropic mechanisms without classical side effects, earning collaborative interest from neuroimmunology groups. The peptide became a staple for her stress-resilience and emotional-cognitive balance studies.
What emotional or cognitive deficit under chronic stress might the Selank 10mg Peptide help you normalize more selectively in your behavioral or neurochemical models?
What Exactly Is the Selank 10mg Peptide?
The Selank 10mg Peptide is a synthetic heptapeptide analog of the natural immunomodulatory tetrapeptide tuftsin (Thr-Lys-Pro-Arg), extended and stabilized with Pro-Gly-Pro at the C-terminus to enhance duration and CNS penetration.
Core specifications:
Quantity: 10mg sterile lyophilized powder per vial—ideal for dose-response curves, behavioral paradigms, chronic administration, or combination protocols
Purity: ≥99% (third-party verified by HPLC and Mass Spectrometry)
Sequence: Thr-Lys-Pro-Arg-Pro-Gly-Pro (TKPRPGP)
Molecular Formula: C₃₃H₅₇N₁₁O₉
Molecular Weight: ≈751.9 Da
Form: White, sterile lyophilized powder optimized for reconstitution
Storage: -20°C long-term; 2-8°C after reconstitution with bacteriostatic water or PBS
COA: Full batch-specific analytical report included
Mechanistically, Selank 10mg Peptide modulates GABAergic neurotransmission (altering GABA receptor subunit expression), preserves enkephalins by inhibiting their degradation, upregulates BDNF in stress-sensitive regions, influences serotonin and dopamine balance under stress, and exerts immunomodulatory effects (e.g., IL-6 modulation) without broad immune suppression.
Here are professional examples of Selank research-grade lyophilized vials in sterile glass packaging, showcasing the clean, high-quality presentation typical for lab-grade peptides:
Why Researchers Choose Selank 10mg Peptide for Anxiolytic and Nootropic Studies
Selank's standout profile—rapid, non-sedating anxiolysis combined with cognitive support and stress-protective actions—makes it ideal for modeling balanced emotional-cognitive states.
Preclinical highlights:
Pronounced reduction in anxiety-like behaviors (elevated plus maze, open field) without myorelaxation or sedation
Restoration of cognitive function (memory, learning) impaired by stress or inflammation
Upregulation of BDNF and normalization of GABAergic gene expression
Modulation of enkephalinergic and serotonergic systems under stress
Potential synergy with other nootropics (e.g., Semax) for enhanced resilience
Immunomodulatory effects without broad suppression
Sourcing from Cali BioLab Peptides ensures USA-certified quality, fast domestic shipping (same/next-day processing), secure checkout, and strict research-only compliance—essential for reproducible, grant-compliant work.
How to Incorporate Selank 10mg Peptide into Lab Protocols
Reconstitution is straightforward:
Equilibrate vial to room temperature.
Add 1-2 mL bacteriostatic water or sterile PBS; gently swirl.
Prepare stocks (e.g., 2-5 mg/mL) and dilute for working concentrations (typically 50-500 μg/kg in vivo, often intranasal or IP; μg/mL in vitro).
Aliquot and freeze at -80°C for long-term use.
Applications include:
Anxiety paradigms (elevated plus maze, light-dark box, novelty suppressed feeding)
Frequently Asked Questions About Selank 10mg Peptide
Q: How does Selank differ from benzodiazepines in research models? A: Selank provides anxiolysis without sedation, myorelaxation, tolerance, or rebound; it enhances GABA tone subtly while preserving cognitive function.
Q: What dosing ranges are common in preclinical literature? A: In-vivo studies often use 50-500 μg/kg (intranasal, IP, or SC); effects frequently show inverted U-shaped dose-response.
Q: Is Selank suitable for cognitive impairment under stress models? A: Yes—preclinical data demonstrate restoration of memory/learning impaired by chronic stress or inflammation.
Q: Stability post-reconstitution? A: Stable for weeks refrigerated; freeze aliquots for longer storage.
Q: Can Selank be combined with Semax or other nootropics? A: Yes—synergistic anxiolytic-nootropic effects are commonly explored in literature.
Q: How to verify batch quality? A: Cross-reference the provided COA on the product page.
What Emotional-Cognitive Balance Question Could Selank 10mg Peptide Help You Answer?
With increasing focus on non-sedating anxiolytics and stress-resilient cognition, what specific anxiety-memory interaction, GABAergic modulation, or BDNF dynamic might the Selank 10mg Peptide illuminate in your research? Could it refine models of generalized anxiety or neurasthenia analogs?
Share your research perspective—the dialogue drives discovery.
In summary, the Selank 10mg Peptide from Cali BioLab Peptides is a uniquely balanced tool for anxiolytic and nootropic pathway research. With exceptional purity, reliable supply, and proven multifaceted utility, it's poised to support your 2026 investigations into calm clarity.
MOTS-c 10mg Peptide – The Mitochondrial-Derived Peptide Powering Metabolic Resilience & Longevity Research
What if a tiny, 16-amino-acid peptide encoded directly inside the mitochondrial genome could act as a master metabolic regulator—boosting NAD+ salvage, activating AMPK, enhancing fat oxidation, improving insulin sensitivity, protecting against age-related physical decline, and even mimicking some benefits of exercise in laboratory models? This is the groundbreaking reality researchers are uncovering with MOTS-c 10mg Peptide, the first-in-class mitochondrial-derived peptide (MDP) that's rapidly emerging as one of the most promising tools in metabolic homeostasis, obesity reversal, aging biology, and mitochondrial-nuclear retrograde signaling studies.
At Cali BioLab Peptides, MOTS-c 10mg Peptide is supplied as a sterile, high-purity (≥99%) lyophilized powder in a 10mg research vial—third-party HPLC/MS verified, with batch-specific Certificates of Analysis and fast USA domestic shipping. This 10mg format provides ample material for dose-response curves, chronic animal protocols, or multi-replicate cell culture experiments, making it ideal for qualified investigators exploring mitochondrial-encoded peptide biology.
Strict Disclaimer: For laboratory and scientific research use only. Not for human consumption, therapeutic, diagnostic, veterinary, or any non-research application. Strictly intended for qualified researchers conducting in-vitro, ex-vivo, or ethically approved animal model studies. Cali BioLab Peptides maintains full regulatory compliance.
The Experiment That Redefined Exercise-Mimetic Research: Dr. Chang’s High-Fat Diet Mouse Model
In a mitochondrial metabolism and aging lab at a top-tier U.S. university, Dr. Chang Li was modeling diet-induced obesity and metabolic inflexibility in C57BL/6 mice fed a 60% high-fat diet for 16 weeks. Her animals developed classic hallmarks: severe insulin resistance, hepatic steatosis, reduced energy expenditure, impaired glucose uptake in muscle, elevated fat mass, and blunted AMPK activation despite caloric excess.
Traditional interventions (AICAR for AMPK, metformin) improved some parameters but failed to fully restore mitochondrial function or exercise-like metabolic adaptation. Chang had followed the seminal 2015 Lee et al. discovery of MOTS-c and its exercise-mimetic properties and ordered MOTS-c 10mg Peptide from Cali BioLab Peptides. The 10mg vial arrived lyophilized with a COA confirming 99.5% purity and structural integrity.
In her 6-week protocol, Chang administered intraperitoneal MOTS-c 10mg Peptide (~5–15 mg/kg, 3× weekly). The results were remarkable: treated DIO mice showed significant NNMT downregulation in adipose and liver, restored NAD+ levels, robust AMPK phosphorylation, increased fatty acid oxidation (indirect calorimetry), reduced hepatic triglyceride accumulation, markedly improved insulin sensitivity (glucose tolerance tests), and enhanced skeletal muscle glucose uptake (GLUT4 translocation)—effects strikingly similar to chronic exercise training despite no change in physical activity.
Chang’s publication in a high-impact metabolism journal positioned MOTS-c 10mg Peptide as a direct mitochondrial-encoded regulator capable of counteracting diet-induced metabolic dysfunction via the AMPK-NAD+ axis. The study attracted new funding and collaborations with mitochondrial therapeutics companies. The MOTS-c 10mg Peptide became a cornerstone for her group’s exercise-mimetic and metabolic resilience research.
What Exactly Is MOTS-c 10mg Peptide?
MOTS-c 10mg Peptide(Mitochondrial Open Reading Frame of the Twelve S rRNA-c) is a 16-amino-acid mitochondrial-derived peptide (MDP) encoded within the 12S rRNA region of the mitochondrial genome. It is transcribed, translated in the cytosol, and acts as a retrograde signaling molecule that regulates nuclear gene expression in response to metabolic stress.
Key product specifications:
Quantity: 10mg sterile lyophilized powder per vial—ideal for dose-response curves, chronic administration, or multiple animal/cell cohorts
Purity: ≥99% (third-party verified by HPLC and Mass Spectrometry)
Storage: –20 °C long-term; 2–8 °C after reconstitution with bacteriostatic water or PBS
COA: Batch-specific analytical report included
In research models, MOTS-c 10mg Peptide translocates to the nucleus under metabolic stress to regulate gene expression via AMPK activation, promoting fatty acid β-oxidation, glucose uptake (GLUT4), and mitochondrial biogenesis while suppressing pro-inflammatory pathways.
Here are professional examples of MOTS-c 10mg Peptide research-grade lyophilized vials in sterile glass packaging, showcasing the clean, high-quality presentation typical for lab use:
How Does MOTS-c 10mg Peptide Work in Biological Systems?
MOTS-c 10mg Peptide functions as a retrograde signaling peptide from mitochondria to nucleus:
Under metabolic stress (high-fat diet, aging, exercise), MOTS-c is translated in the cytosol and translocates to the nucleus.
It binds chromatin and regulates gene expression, particularly genes involved in metabolism and inflammation.
Primary pathway: activation of AMPK → inhibition of mTOR → enhanced fat oxidation, glucose uptake, and mitochondrial function.
Usage and Reconstitution Guidelines for MOTS-c 10mg Peptide
Allow vial to reach room temperature.
Add 1–2 mL bacteriostatic water or sterile PBS; gently swirl.
Prepare stock solutions (e.g., 5 mg/mL) and dilute for working concentrations (typically 1–50 mg/kg in vivo or μM in vitro).
Aliquot immediately → store at –80 °C. Thawed aliquots stable 2–8 °C for days.
Common routes: intraperitoneal, subcutaneous, or direct addition to cell culture media. Use sterile technique.
Frequently Asked Questions About MOTS-c 10mg Peptide
Q: How does MOTS-c 10mg Peptide differ from NAD+ precursors like NMN or NR? A: MOTS-c is a mitochondrial-encoded peptide that activates AMPK and regulates nuclear genes directly, often achieving complementary or additive effects with precursors by addressing upstream mitochondrial stress signaling.
Q: What dosing ranges are common in preclinical literature? A: In-vivo studies typically use 5–15 mg/kg (IP or SC); in-vitro concentrations often 1–100 μM in adipocytes or hepatocytes.
Q: Is MOTS-c 10mg Peptide cell-permeable and stable? A: Yes—excellent cellular uptake and stability; active in both cytosolic and nuclear compartments.
Q: Suitable for muscle or exercise-mimetic models? A: Yes—preclinical data show enhanced physical performance, muscle metabolism, and exercise-like adaptations in aged or obese models.
Q: How to verify batch quality? A: Match the provided COA on the product page.
One Question That Could Shape Your Next Metabolic or Longevity Study
If you could directly activate mitochondrial-nuclear retrograde signaling right now in a metabolic stress or aging model, which endpoint—fat oxidation, insulin sensitivity, NAD+ preservation, or exercise-like performance—would you target first, and what key assay would you use to prove efficacy?
Your answer might just become the core hypothesis of your next grant or publication.
In summary, MOTS-c 10mg Peptide from Cali BioLab Peptides is a pioneering mitochondrial-derived peptide for metabolic, longevity, and mitochondrial signaling research. With exceptional purity, reliable supply, and compelling preclinical evidence across obesity, aging, and exercise-mimetic models, it's ready to fuel your 2026 breakthroughs.
Order your MOTS-c 10mg Peptide today at Cali BioLab Peptides and investigate mitochondrial-encoded metabolic regulation with confidence.
Bacteriostatic Mixing Water 3ml – Research-Grade Solution
Bluewell’s Bacteriostatic Mixing Water (3ml) is manufactured to the highest laboratory standards for precision and reliability. This sterile, nonpyrogenic solution contains 0.9% benzyl alcohol, helping inhibit bacterial growth and maintain sample integrity during use.
Supplied in a 3ml multi-dose vial, this smaller volume is perfect for reconstituting a single peptide vial, reducing waste while maintaining sterility and accuracy.
Key Features
Accurate Measurement – Each 3ml vial is filled with precision for consistent laboratory results.
Bacteriostatic Formula – Contains 0.9% benzyl alcohol to help maintain sterility after opening.
pH Balanced – Maintained at approximately 5.7 (within a 4.5–7.0 range) for optimal peptide reconstitution.
Ideal for Single-Vial Use – Perfect for reconstituting one peptide vial without leftover solution.
Compact & Convenient – Minimizes waste while retaining the same high-grade quality as larger vials.
Ideal Storage – Store between 20°C–25°C to preserve quality.
Why Choose Bluewell’s Bacteriostatic Water?
Trusted by research professionals across the UK
Manufactured under strict sterile conditions
Convenient size for single-use or small-scale peptide preparation
Backed by Bluewell’s reliable customer support
Safety and Compliance
Bluewell products are intended strictly for laboratory research purposes only.
This solution is not for human or veterinary use.
Use must comply with all applicable laboratory safety standards and regulations.
Glow Blend 70mg – High-Purity Research Peptide Formulation
Glow Blend is a proprietary research peptide formulation combining BPC-157 (10mg), TB-500 (10mg), and GHK-Cu (50mg) — three widely studied peptides known for their potential synergy in research related to cellular regeneration, tissue healing, and skin repair.
Each vial is supplied in lyophilised (freeze-dried) form for optimal stability and shelf life. Every batch is tested at >99.1% purity (HPLC-verified) and provided with a full Certificate of Analysis (COA).
The 70mg blend is designed for advanced research projects requiring a combination of regenerative and anti-inflammatory peptide agents.
What is Glow Blend?
Glow Blend is formulated for laboratory studies focused on cellular repair, inflammation regulation, and oxidative stress response.
Each component contributes distinct properties:
BPC-157 (10mg): A synthetic peptide fragment studied in preclinical models for its influence on angiogenesis, fibroblast activity, and gastrointestinal tissue repair.
TB-500 (10mg): A synthetic version of Thymosin Beta-4, researched for its ability to promote cellular migration, tissue regeneration, and inflammation control via actin modulation.
GHK-Cu (500mg): A copper-binding peptide associated with collagen production, skin rejuvenation, and antioxidant activity in cosmetic and wound-healing research.
Together, these compounds create a versatile peptide blend explored in areas such as dermal regeneration, soft tissue healing, and cellular stress management.
Scientific Identifiers
BPC-157
CAS Number: 137525-51-0
Molecular Formula: C₆₂H₉₈N₁₆O₂₂
Molecular Weight: 1419.56 g/mol
Purity: >99.1%
TB-500
CAS Number: 77591-33-4
Molecular Formula: C₂₁₂H₃₅₀N₅₆O₇₈S
Molecular Weight: 4963.44 g/mol
Purity: >99.1%
GHK-Cu
CAS Number: 89030-95-5
Molecular Formula: C₁₄H₂₃CuN₆O₄
Molecular Weight: 401.91 g/mol
Purity: >99.1%
Total Blend Weight: 70mg
Form: Lyophilised Solid
Catalogue Number: BWP-GLOW-70
Storage: Store at −20°C, protected from light
Usage and Reconstitution
Glow Blend is supplied as a lyophilised powder to ensure long-term stability during storage and transport. For research use, it may be reconstituted with bacteriostatic water or another appropriate solvent according to standard peptide handling protocols. For full preparation guidelines, refer to our Peptide Reconstitution Guide.
Research Applications of Glow Blend
Laboratory studies have explored Glow Blend and its individual components in the following research contexts:
Tissue Regeneration & Healing – Examined for potential effects on collagen formation, fibroblast activation, and wound closure mechanisms.
Dermal and Hair Research – GHK-Cu has been studied for its role in improving skin texture and stimulating hair follicle activity.
Anti-Inflammatory Pathways – BPC-157 and TB-500 may assist in regulating inflammatory cytokines and oxidative stress responses.
Oxidative Stress & Antioxidant Support – GHK-Cu has demonstrated antioxidant properties in vitro, helping reduce free radical damage and support cell renewal.
Scientific references are available on request or through our internal research archive.
Why Order Glow Blend from Bluewell Peptides?
Verified >99.1% purity (HPLC-tested)
COA included with every batch
Fast and secure USA shipping
Transparent research-only supplier
Excellent support and verified reviews
CJC-1295 No DAC 5mg – High-Purity Research Peptide
CJC-1295 No DAC (also known as MOD GRF 1-29) is a synthetic research peptide widely studied in preclinical and laboratory settings for its role in stimulating growth hormone release through GHRH receptor activation. Supplied in lyophilised (freeze-dried) form to preserve stability, this compound is HPLC-verified at >99% purity and accompanied by full Certificates of Analysis (COAs).
What is CJC-1295 No DAC?
CJC-1295 No DAC is a shorter-acting analogue of growth hormone–releasing hormone (GHRH), designed to support research into pulsatile GH release without extended half-life modification. It has been investigated in models related to endocrine function, metabolism, and cellular recovery. Unlike long-acting DAC variants, CJC-1295 No DAC produces a shorter but more physiologically relevant GH pulse, making it a valuable peptide in certain research contexts.
Scientific Identifiers
Product Name: CJC-1295 No DAC 5mg
Catalogue Number: BWP-CJC-ND5
CAS Number: 863288-34-0
Molecular Formula: C152H252N44O42
Molecular Weight: 3367.9 g/mol
Form: Lyophilised Solid
Purity: >99% (HPLC Verified)
Storage: Store at −20°C in a dry, dark place
Unit Size: 5mg
Usage and Reconstitution
CJC-1295 No DAC is supplied as a lyophilised solid for maximum stability. For research applications, it may be reconstituted with bacteriostatic water or a suitable solvent according to laboratory protocols. Avoid repeated freeze–thaw cycles. For guidance, see our [Reconstitution Guide].
Research Applications of CJC-1295 No DAC
CJC-1295 No DAC has been investigated in preclinical and laboratory studies for its potential influence on:
Growth Hormone Secretion Research – Studied for its role in stimulating GH release via GHRH receptor activation.
Endocrine Function Studies – Used to study pituitary activity and hormone regulation.
Metabolic & Recovery Research – Explored for its effects on protein synthesis, recovery, and cellular metabolism.
References available on request or in our research archive.
Why Order CJC-1295 No DAC from Bluewell Peptides?
Verified >99% purity, HPLC-tested
COA provided with every batch
Secure checkout and fast USA delivery
Trusted research-focused supplier
Excellent customer support
The Hidden Fat-Burning Switch: How a Small Molecule Could Flip Metabolism into High Gear in Research Models
What if a tiny, selective inhibitor could silence an enzyme that's quietly sabotaging NAD+ levels, slowing fat oxidation, and locking away energy in white adipose tissue—potentially allowing cells to burn stored fat more efficiently, restore youthful metabolic flexibility, and protect against diet-induced obesity in laboratory models? This is the intriguing possibility driving growing interest in 5-Amino-1MQ 10mg Peptide, a small-molecule research compound studied as a potent inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme implicated in age- and obesity-related metabolic inefficiency.
At Cali BioLab Peptides, we offer 5-Amino-1MQ 10mg Peptide as a high-purity (≥99%), sterile lyophilized powder in a 10mg vial—third-party HPLC/MS verified, batch-specific COAs provided, and shipped fast within the USA. This research-grade compound empowers qualified investigators to explore NNMT inhibition, NAD+ preservation, fat oxidation pathways, and metabolic reprogramming in controlled in-vitro, ex-vivo, or approved animal model studies.
Strict Disclaimer: For laboratory and scientific research use only. Not for human consumption, therapeutic, diagnostic, veterinary, or any non-research application. Strictly intended for qualified researchers conducting in-vitro, ex-vivo, or ethically approved animal model studies. Cali BioLab Peptides maintains full regulatory compliance.
The Obesity Reversal Experiment: Dr. Neha’s High-Fat Diet Mouse Model That Changed the Game
In a metabolic disease research group at a major U.S. university, Dr. Neha Patel was modeling diet-induced obesity (DIO) in C57BL/6 mice fed a 60% high-fat diet for 12 weeks. Her animals developed severe insulin resistance, massive white adipose tissue expansion, reduced energy expenditure, elevated NNMT expression in fat and liver, depleted NAD+ levels, and stalled weight loss despite caloric restriction attempts.
Precursor-based NAD+ boosters (NMN, NR) helped modestly but couldn't overcome the NNMT-driven "methyl sink" that consumed nicotinamide and impaired fat oxidation. Neha sourced 5-Amino-1MQ 10mg Peptide from Cali BioLab Peptides after reviewing key 2018 studies on NNMT inhibitors. The 10mg vial arrived lyophilized with a COA confirming 99.4% purity.
In her 8-week intervention, Neha administered oral or intraperitoneal 5-Amino-1MQ 10mg Peptide (scaled ~10-30 mg/kg/day). The results were striking: treated DIO mice showed significant NNMT inhibition in adipose and liver, restored NAD+ levels, increased oxygen consumption and fat oxidation (indirect calorimetry), reduced white adipose mass (DEXA/MRI), improved insulin sensitivity (lower HOMA-IR), and accelerated body weight loss—even on the high-fat diet—without muscle wasting or overt toxicity.
Neha’s publication in a high-impact metabolism journal demonstrated that 5-Amino-1MQ 10mg Peptide could reverse DIO-induced metabolic dysfunction by breaking the NNMT-NAD+ vicious cycle, earning her team expanded funding and collaborations with NAD+ therapeutics companies. The compound became essential for her group’s obesity reversal and metabolic reprogramming studies.
What Exactly Is 5-Amino-1MQ 10mg Peptide?
5-Amino-1MQ 10mg Peptide (also written as 5-Amino-1-methylquinolinium or 5-Amino-1MQ) is a small-molecule research compound functioning as a selective, cell-permeable inhibitor of nicotinamide N-methyltransferase (NNMT).
Key product specifications:
Quantity: 10mg sterile lyophilized powder per vial—ideal for dose-response curves, chronic administration in small cohorts, or multiple cell/animal replicates
Purity: ≥99% (third-party verified by HPLC and Mass Spectrometry)
Molecular Formula: C₁₀H₁₁N₂⁺ (cationic form)
Molecular Weight: ≈159.21 Da (as cation)
CAS Number: Not universally standardized (research compound; often referenced in NNMT inhibitor literature)
Form: White to off-white lyophilized powder
Storage: –20 °C long-term; 2–8 °C after reconstitution with bacteriostatic water or PBS
COA: Batch-specific analytical report included
In research, 5-Amino-1MQ 10mg Peptide inhibits NNMT, preventing the methylation of nicotinamide (a NAD+ precursor) into 1-methylnicotinamide. This preserves NAD+ availability, boosts sirtuin activity, enhances mitochondrial function, and shifts metabolism toward fat oxidation.
Here are professional examples of 5-Amino-1MQ 10mg Peptide research-grade lyophilized vials in sterile glass packaging, illustrating the clean, high-quality presentation typical for lab use:
How Does 5-Amino-1MQ 10mg Peptide Work in Biological Systems?
5-Amino-1MQ 10mg Peptide selectively binds and inhibits NNMT, an enzyme highly expressed in adipose tissue, liver, and other metabolic organs. NNMT catalyzes the transfer of a methyl group from S-adenosylmethionine (SAM) to nicotinamide, producing 1-methylnicotinamide and depleting the NAD+ salvage pathway precursor pool.
By blocking this reaction, 5-Amino-1MQ 10mg Peptide:
Preserves nicotinamide for NAD+ resynthesis via salvage pathways
Elevates intracellular NAD+ levels
Activates NAD+-dependent sirtuins (SIRT1, SIRT3) for metabolic regulation
Enhances mitochondrial fatty acid oxidation and energy expenditure
Reduces white adipose tissue accumulation and adipocyte size
Improves insulin sensitivity and glucose handling in models
These effects are concentration-dependent and often fit sigmoidal dose-response curves in adipocyte and animal studies.
Research Applications of 5-Amino-1MQ 10mg Peptide
5-Amino-1MQ 10mg Peptide is applied in:
Obesity and metabolic syndrome models (DIO, high-fat diet reversal)
NAD+ metabolism and sirtuin activation studies
Fat oxidation and mitochondrial bioenergetics (indirect calorimetry, Seahorse)
Adipocyte differentiation and lipolysis assays
Liver steatosis (NAFLD) and insulin resistance analogs
Aging-related metabolic decline and frailty research
Key endpoints where 5-Amino-1MQ 10mg Peptide excels:
Reduction in body weight and adipose mass
Restoration of NAD+/NADH ratio (LC-MS/MS)
Increased oxygen consumption and energy expenditure
Decreased NNMT activity and 1-methylnicotinamide levels
Enhanced mitochondrial function and reduced ROS
Usage and Reconstitution Guidelines for 5-Amino-1MQ 10mg Peptide
Allow vial to reach room temperature.
Add 1–2 mL bacteriostatic water or sterile PBS; gently swirl to dissolve.
Prepare stock solutions (e.g., 5 mg/mL) and dilute for working concentrations (typically 1–100 μM in vitro or 10–50 mg/kg in vivo).
Aliquot immediately and store at –80 °C; thawed aliquots stable 2–8 °C for days.
Common routes: oral gavage (high bioavailability in models), intraperitoneal, or direct addition to cell culture media.
Frequently Asked Questions About 5-Amino-1MQ 10mg Peptide
Q: How does 5-Amino-1MQ 10mg Peptide differ from NAD+ precursors like NMN or NR? A: It directly inhibits NNMT to preserve endogenous nicotinamide for NAD+ salvage, often achieving more efficient NAD+ elevation in adipose/liver tissues than precursors alone.
Q: What dosing ranges are common in preclinical literature? A: In-vivo studies often use 10–50 mg/kg (oral or IP); in-vitro concentrations typically 1–100 μM in adipocytes or hepatocytes.
Q: Is 5-Amino-1MQ 10mg Peptide cell-permeable? A: Yes—studies show excellent membrane permeability and intracellular NNMT inhibition in adipocytes.
Q: Suitable for muscle or mitochondrial studies? A: Yes—emerging data link NNMT inhibition to improved muscle NAD+ and strength in aging models.
Q: Stability post-reconstitution? A: Stable for weeks refrigerated when aliquoted; freeze for longer storage.
Q: How to verify batch quality? A: Cross-reference the provided COA on the product page.
What Metabolic Puzzle Could 5-Amino-1MQ 10mg Peptide Help You Solve?
With NNMT emerging as a key driver of metabolic inefficiency, what specific fat oxidation pathway, NAD+ preservation mechanism, or obesity-related resistance might 5-Amino-1MQ 10mg Peptide illuminate in your models? Could it redefine how you approach adipose tissue reprogramming or insulin sensitivity research?
Share your research angle—the scientific dialogue drives discovery.
In summary, 5-Amino-1MQ 10mg Peptide from Cali BioLab Peptides is a selective NNMT inhibitor with compelling potential in metabolic and longevity studies. With superior purity, reliable supply, and growing preclinical evidence, it's ready to support your 2026 investigations into fat metabolism and NAD+ biology.
Order your 5-Amino-1MQ 10mg Peptide today at Cali BioLab Peptides and target NNMT with precision in your experiments.
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