Human Alpha-1-antitrypsin (SERPINA1) ELISA Kit

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AE20069HU
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Product Name Human Alpha-1-antitrypsin (SERPINA1) ELISA Kit
Description alpha1-antitrypsin, an acute phase protein, is the prototypic member of the serpin super family and a major inhibitor of serine proteases. As an acute phase protein, alpha 1-antitrypsin is thought to play an important role in limiting host tissue injury at sites of inflammation. A1AT is a 52-kDa serpin (serine protease inhibitor), and, in medicine, it is considered the most prominent serpin; the terms alpha 1-antitrypsin and protease inhibitor (Pi) are often used interchangeably.Like all serine protease inhibitors, A1AT has a characteristic secondary structure of beta sheets and alpha helices. Mutations in these areas can lead to non-functional proteins that can polymerise and accumulate in the liver (infantile hepatic cirrhosis). This assay has high sensitivity and excellent specificity for detection of Human SERPINA1. No significant cross-reactivity or interference between Human SERPINA1 and analogues was observed.
Synonyms A1A, A1-AT, AAT, MGC23330, MGC9222, PI, PI1, PRO2275, OTTHUMP00000197150|protease inhibitor 1 (anti-elastase), alpha-1-antitrypsin|serine (or cysteine) proteinase inhibitor, clade A, member 1|serine, Serpin Peptidase Inhibitor,Clade A(Alpha-1 Antiproteinase/AntiTrypsin)Member 1
Method Sandwich ELISA
Detection Range 6.25-400 ng/mL
Sensitivity 2.83 ng/mL
Reactivity Human
Sample Types Serum, Plasma, Other biological fluids.
Background alpha1-antitrypsin, an acute phase protein, is the prototypic member of the serpin super family and a major inhibitor of serine proteases. As an acute phase protein, alpha 1-antitrypsin is thought to play an important role in limiting host tissue injury at sites of inflammation.
A1AT is a 52-kDa serpin (serine protease inhibitor), and, in medicine, it is considered the most prominent serpin; the terms alpha 1-antitrypsin and protease inhibitor (Pi) are often used interchangeably.Like all serine protease inhibitors, A1AT has a characteristic secondary structure of beta sheets and alpha helices. Mutations in these areas can lead to non-functional proteins that can polymerise and accumulate in the liver (infantile hepatic cirrhosis).
Supplier Abebio

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