Alpha 1 Antitrypsin [9041-92-3]
16-16-011609
Protein IDP01009
Product group Proteins / Signaling Molecules
Overview
- SupplierAthens Research
- Product NameAlpha 1 Antitrypsin [9041-92-3]
- Delivery Days Customer9
- Applications SupplierProteolytic Inhibition studies, Antibody detection, ELISA Standards, Potein Structure Studies, A1AT deficiency research, Antisera Production, In Vitro Diagnostics
- CertificationResearch Use Only
- Estimated Purity≥95% by SDS-PAGE
- Protein IDP01009
- Protein NameAlpha-1-antitrypsin
- Scientific DescriptionAlpha-1 antitrypsin is a glycoprotein primarily produced by the liver and circulates in plasma at concentrations of 95–350 mg per 100 ml. As a member of the serpin superfamily, A1AT’s main function is to protect tissues, especially in the lungs, from proteolytic damage by inhibiting enzymes such as neutrophil elastase. By binding to and inactivating elastase, A1AT prevents the breakdown of elastin in connective tissue, thereby preserving lung structure and function. Deficiency of A1AT, most often due to mutations in the SERPINA1 gene, leads to unregulated elastase activity. This can cause early-onset pulmonary emphysema and chronic obstructive pulmonary disease (COPD), as well as juvenile or adult liver cirrhosis due to accumulation of abnormal A1AT in the liver. Less commonly, deficiency can result in skin disorders like panniculitis. Clinically, A1AT levels rise during inflammation, malignancy, liver disease, pregnancy, after surgery, and with oral contraceptive use. Measurement of A1AT, often alongside ceruloplasmin, aids in distinguishing different liver disorders. Therapeutically, purified A1AT is used for augmentation therapy in individuals with severe deficiency, and research continues into its broader anti-inflammatory and immunomodulatory applications.
- Shelf life instructionmore then 1 year
- SourceSource human plasma non-reactive for HBsAG, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.
- Storage Instruction≤ -20°C
- UNSPSC41116100
References
- Schevenels, G., et al., (2024), 'A brain-specific angiogenic mechanism enabled by tip cell specialization', Nature, 628: pp 863-871.Read this paper
- Hiroyuki, M. et al., (2024), 'Hair follicle aging is driven by transepidermal elimination of stem cells via COL17A1 proteolysis', Science 351: aad4395.Read this paper
- Cui, C., et al., (2021), 'Neutrophil elastase selectively kills cancer cells and attenuates tumorigenesis', Cell, 184: pp 3163–3177Read this paper
- Geiger, S., et al., (2019), 'Alpha-1 Antitrypsin-Expressing Mesenchymal Stromal Cells Confer a Long-Term Survival Benefit in a Mouse Model of Lethal GvHD', Molecular Therapy, 27(8): pp 1436-1451.Read this paper
- Borel, F., et al., (2017), 'Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of a-1 Antitrypsin Deficiency', Molecular Therapy, 25(11): pp 2477 - 2489.Read this paper