ARG81189

Rat alpha 2 Macroglobulin ELISA Kit

Rat alpha 2 Macroglobulin ELISA Kit for ELISA and Rat

Overview

Product Description ARG81189 Rat Alpha-2-Macroglobulin ELISA is an Enzyme Immunoassay kit for the quantification of Rat Alpha-2-Macroglobulin in serum, plasma, cell culture and urine.
Tested Reactivity Rat
Tested Application ELISA
Target Name alpha 2 Macroglobulin
Conjugation HRP
Conjugation Note Substrate: TMB and read at 450 nm
Sensitivity less than 0.1 ng/ml
Sample Type Serum, plasma, cell culture and urine.
Standard Range 0.156 - 10 ng/ml
Sample Volume 50 µl
Alternate Names CPAMD5; Alpha-2-macroglobulin; S863-7; FWP007; Alpha-2-M; A2MD; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 5

Application Instructions

Assay Time ~ 4 hours

Properties

Form 96 well
Storage Instruction Store the kit at 2-8°C. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 24153 Rat A2M

Swiss-port # P06238 Rat Alpha-2-macroglobulin

Gene Symbol A2m
Gene Full Name alpha-2-macroglobulin
Background Alpha-2-macroglobulin is a protease inhibitor and cytokine transporter. It inhibits many proteases, including trypsin, thrombin and collagenase. A2M is implicated in Alzheimer disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. [provided by RefSeq, Jul 2008]
Function Is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase. [UniProt]
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