Overview
ARA-290 (Cibinetide) is a synthetic peptide derived from the helix B domain of erythropoietin (EPO). It has been structurally modified to enable selective interaction with the EPOR-CD131 receptor complex, commonly referred to as the innate repair receptor (IRR), without engaging pathways associated with erythropoiesis.
ARA-290 is an 11-amino-acid peptide engineered from the helix B surface region of erythropoietin. In laboratory settings, it is utilised as a model compound in research involving EPO-derived peptides and EPOR-CD131 receptor interactions.
Chemical reference information: CAS number: 1208243-50-8; Molecular formula: C₅₁H₈₄N₁₆O₂₁; Molecular weight: 1257.3 g/mol. These reference identifiers describe the formulation; the batch-specific analytical record identifies the supplied material.
Reference conditions for unreconstituted research material are −20°C with moisture and direct light excluded. Use the storage instructions on the supplied batch record for the actual presentation, and record any change of physical state or storage conditions.
Where laboratory preparation is required, use an appropriate validated solvent and aseptic peptide-handling procedure. Solvent compatibility, final concentration, and post-preparation storage depend on the specific formulation and experimental protocol. The catalog strength is the compound amount, not the concentration of a prepared solution.
NORVEXA Bioscience batch documentation can be requested using the printed reference and lot number. Review identity, analytical purity, presentation, and handling specifications before including a material in a laboratory workflow.
ARA-290 10 mg is offered as a NORVEXA research pen. The selected strength refers to the compound content of this pen reference. Request the matching batch record for identity, analytical specifications, and presentation details.
Handling and storage
Reference conditions for unreconstituted research material are −20°C with moisture and direct light excluded. Use the storage instructions on the supplied batch record for the actual presentation, and record any change of physical state or storage conditions.
Where laboratory preparation is required, use an appropriate validated solvent and aseptic peptide-handling procedure. Solvent compatibility, final concentration, and post-preparation storage depend on the specific formulation and experimental protocol. The catalog strength is the compound amount, not the concentration of a prepared solution.
NORVEXA Bioscience batch documentation can be requested using the printed reference and lot number. Review identity, analytical purity, presentation, and handling specifications before including a material in a laboratory workflow.