CH Peptides
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B-12 MIC refers to a methylcobalamin formulation frequently researched for its biochemical attributes and bioavailability characteristics. It does not have designated research or development codes in pharmaceutical settings or alternative scientific naming conventions commonly used in literature.
The compound does not involve a specific peptide sequence but comprises a cobalamin core with a modified methyl group. It is characterized by its coordination to cobalt, forming a corrin ring that directly influences its biological activity.
Methylcobalamin is notably studied for its involvement in pathways such as methionine synthesis. It acts as a coenzyme in the conversion of homocysteine to methionine, leveraging the enzyme methionine synthase. Its interaction does not fit typical receptor-ligand models but is integral to enzymatic function and genetic regulation, including DNA synthesis pathways.
Methylcobalamin is moderately soluble in water, with a suggested reconstitution concentration of approximately 1mg/mL for experimental contexts. It remains stable in lyophilized form when stored adequately under desiccated conditions and preserves stability for extended periods post-reconstitution if stored at low temperatures.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or preventive applications.
B-12 MIC refers to a methylcobalamin formulation frequently researched for its biochemical attributes and bioavailability characteristics. It does not have designated research or development codes in pharmaceutical settings or alternative scientific naming conventions commonly used in literature.
The compound does not involve a specific peptide sequence but comprises a cobalamin core with a modified methyl group. It is characterized by its coordination to cobalt, forming a corrin ring that directly influences its biological activity.
Methylcobalamin is notably studied for its involvement in pathways such as methionine synthesis. It acts as a coenzyme in the conversion of homocysteine to methionine, leveraging the enzyme methionine synthase. Its interaction does not fit typical receptor-ligand models but is integral to enzymatic function and genetic regulation, including DNA synthesis pathways.
Methylcobalamin is moderately soluble in water, with a suggested reconstitution concentration of approximately 1mg/mL for experimental contexts. It remains stable in lyophilized form when stored adequately under desiccated conditions and preserves stability for extended periods post-reconstitution if stored at low temperatures.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or preventive applications.
Chorionic Gonadotropin; commonly abbreviated as HCG. It is a glycoprotein hormone composed of alpha and beta subunits, predominantly characterized in human pregnancy. No specific research codes or development codes are associated with the basic glycoprotein.
HCG is a heterodimeric protein composed of two non-covalently linked subunits: the alpha subunit (92 amino acids) shared with other hormones like LH, FSH, and TSH, and the beta subunit (145 amino acids) which is unique to HCG. The beta subunit contains distinct segments: H-Trp-Met-Ser-Glu-His-Ile-Thr-Arg-Tyr-Leu-... and features specific disulfide bridges essential for activity and stability.
HCG acts as an agonist to the luteinizing hormone/chorionic gonadotropin receptor (LHCG receptor). Binding of HCG to its receptor activates pathways such as the cAMP/PKA signaling cascade, promoting steroidogenesis. EC50 values are variable based on assay and cellular system but are indicative of potent agonist activity.
HCG is soluble in sterile water at concentrations of 1mg/mL for research applications. Upon reconstitution, the solution must be stored at 2-8°C and is stable for up to 24 hours. Lyophilized HCG remains stable at -20°C until reconstitution.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or preventive applications.
Retatrutide is referred to by its research code LY3502970. As of current knowledge, alternative naming conventions in the literature have not been extensively established.
Retatrutide is a peptide compound consisting of 39 amino acids. The exact amino acid sequence is: H-Thr-Lys-Asp-Glu-Leu-Gln-Ala-Ile-Arg-Trp-Leu-Lys-His-Glu-Arg-Asp-His-Gly-Ile-Lys-Lys-Glu-Cys-Leu-Glu-Glu-Val-Leu-Asp-Ser-Leu-Ala-Arg-Ala-Glu-Glu-Arg-OH. Specific modifications include N-terminal acetylation and C-terminal amidation to enhance its activity and stability. It is structurally designed to interact with multiple peptide receptors.
Retatrutide acts as an agonist at multiple receptors, including the GLP-1 receptor (GLP-1R) and the GIP receptor (GIPR), exhibiting multifaceted activity. Its mechanism enhances several intracellular signaling pathways, notably the cAMP/PKA and PI3K/Akt cascades. It demonstrates a unique binding profile, combining activities that influence metabolic pathways associated with glucose and lipid handling.
Retatrutide is notably soluble in sterile water at a concentration of 1mg/mL. For research applications, it is recommended to reconstitute the lyophilized form in an appropriate buffer and store it at -20°C to maintain stability. Once reconstituted, it remains stable for up to 3 weeks if stored under proper conditions.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or preventive applications.
Retatrutide is referred to by its research code LY3502970. As of current knowledge, alternative naming conventions in the literature have not been extensively established.
Retatrutide is a peptide compound consisting of 39 amino acids. The exact amino acid sequence is: H-Thr-Lys-Asp-Glu-Leu-Gln-Ala-Ile-Arg-Trp-Leu-Lys-His-Glu-Arg-Asp-His-Gly-Ile-Lys-Lys-Glu-Cys-Leu-Glu-Glu-Val-Leu-Asp-Ser-Leu-Ala-Arg-Ala-Glu-Glu-Arg-OH. Specific modifications include N-terminal acetylation and C-terminal amidation to enhance its activity and stability. It is structurally designed to interact with multiple peptide receptors.
Retatrutide acts as an agonist at multiple receptors, including the GLP-1 receptor (GLP-1R) and the GIP receptor (GIPR), exhibiting multifaceted activity. Its mechanism enhances several intracellular signaling pathways, notably the cAMP/PKA and PI3K/Akt cascades. It demonstrates a unique binding profile, combining activities that influence metabolic pathways associated with glucose and lipid handling.
Retatrutide is notably soluble in sterile water at a concentration of 1mg/mL. For research applications, it is recommended to reconstitute the lyophilized form in an appropriate buffer and store it at -20°C to maintain stability. Once reconstituted, it remains stable for up to 3 weeks if stored under proper conditions.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or preventive applications.