Anti-a2-Macroglobulin (HRP) Polyclonal Antibody

Cat# M1150-20B-100ug

Size : 100ug

Brand : US Biological

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M1150-20B a2-Macroglobulin (HRP)

Clone Type
Polyclonal
Host
goat
Source
human
Isotype
IgG
Grade
Affinity Purified
Applications
E
Crossreactivity
Ca Hu Mo Po Rb Rt
Shipping Temp
Blue Ice
Storage Temp
-20°C

a2Macroglobulin (a2M) is a large proteinase inhibitor molecule of 718kD, consisting of 4 identical subunits of 185kD each. Produced in hepatocytes and macrophages, plasma concentrations of a2M are typically 2uM in adults, and as high as 6uM in childhood. a2M has the ability to inhibit most enzymes from the serine, metallo, cysteine and aspartate subclasses. It is not a member of the SERPIN family of inhibitors. It belongs to a class of proteins that include pregnancy zone protein (PZP) and the complement proteins C3, C4 and C5. These proteins contain regions of conserved sequence as well as one or more internal b-cysteinyl-_-glutamyl thiolester bonds, which in the case of a2M are susceptible to cleavage by enzymes or by nucleophilic compounds such as methylamine or ammonium ions. Although the precise nature of the interactions is as yet unknown, it is generally thought that cleavage of a bait region within the a2M molecule by an enzyme leads to a conformational change, which then traps and/or covalently binds the enzyme (1,2). The active site of the trapped enzyme is usually still intact and able to cleave small substrates, but is inaccessible to larger natural substrates. The conformational change induced also exposes receptor-binding regions within the molecule, which may be important in the clearance of a2M-enzyme complexes from the circulation. It is thought that the main role of a2M in vivo is that of a “backup” inhibitor and scavenger of proteinases in blood and in tissues (3,4). But it has also been reported to participate in other physiological processes, including regulation of immune function (1,2).||Applications:|Suitable for in ELISA and IEP. Other applications have not been tested.||Recommended Dilutions:|Optimal dilutions to be determined by the researcher.||Rz ratio (Reinheitszahl, A403/A280): |0.29 (determined spectrophotometrically).||Storage and Stability:|Store product at 4°C if to be used immediately within two weeks. For long-term storage, aliquot to avoid repeated freezing and thawing and store at -20°C. Aliquots are stable at -20°C for 12 months after receipt. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Note: Sodium azide is a potent inhibitor of peroxidase and should not be added to HRP conjugates. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Applications
Product Type: Pab|Isotype: IgG|Host: goat|Source: human|Concentration: ~1mg/ml|Form: Supplied as a liquid in a buffered stabilizer solution, 50% glycerol. No preservative added. Labeled with horseradish peroxidase (HRP).|Purity: Purified by affinity chromatography.|Immunogen: Human alpha2-macroglobulin (a2M) purified from human plasma.|Specificity: Recognizes human alpha2 Macroglobulin. Species Crossreactivity: mouse, porcine, canine, rat and rabbit.||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Immunogen
Human alpha2-macroglobulin (a2M) purified from human plasma.
Form
Supplied as a liquid in a buffered stabilizer solution, 50% glycerol. No preservative added. Labeled with horseradish peroxidase (HRP).
Purity
Purified by affinity chromatography.
Specificity
Recognizes human alpha2 Macroglobulin. Species Crossreactivity: mouse, porcine, canine, rat and rabbit.
References
1. Salvesen, G., Pizzo, S.V., Hemostasis and Thrombosis 3rd Edition, eds. R.W. Colman, J. Hirsh, V.J. Marder, E.W. Salzman, pp. 241-258, J.B. Lippincott Co., Philadelphia PA, USA, 1994. 2. Barrett J., Methods in Enzymology, 80: 737-754, 1981. 3. Larsson, L.J., et al., Biochemistry 28: 7636-7643, 1989. 4. Schmidt, B., et al., Thromb Haemostas 62: 1074-1077, 1989. 5. Hoogendoorn, H., et al., Blood 78: 2283-2290, 1991.