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Biolegend/Recombinant Human MIF carrier-free/25 µg/599404
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DescriptionMIFwasdiscoveredinthe1960’sasaT-lymphocyteproductthatinhibitstherandommigrationofmacrophagesduringdelayed-typehypersensitivityresponses.Thiscytokineisasingle,non-glycosylated,115aminoacidspolypeptidethathasaβ-α-βmotif.ItisknownthatMIFinducesinflammatorycytokines,nitricoxideandsuperoxideanions,andregulatesmacrophageandlymphocyteproliferation.TheimmunoregulatoryactivitiesofMIFarebasedupontranscriptionalregulationofinflammatorygeneproducts,modulationofcellproliferationandcellcycleinhibitionofp53-mediatedapoptosis,andanumberofmetaboliceffects.MIFalsodemonstratesbroadregulatorypropertiesandisconsideredasacriticalmediatorofmultipledisorders,includinginflammatoryandautoimmunediseasessuchasrheumatoidarthritis,glomerulonephritis,diabetes,atherosclerosis,sepsis,asthma,andacuterespiratorydistresssyndrome.FurThermore,studieshavehighlightedtheroleofMIFintumOrigenesis.Humancancertissues,includingskin,brain,breast,colon,prostate,andlung-derivedtumorsoverexpressMIF;MIFlevelscorrelatedwithtumoraggressivenessandmetastaticpotential.Therefore,MIFisconsideredaviabletherapeutictargetfortreatinginflammatorydiseasesandneoplasia.Inadditiontoitsphysiologicandpathophysiologicactivities,MIFisknowntoactasatautomeraseandhasacatalyticallyactiveN-terminalprolinethatisinvariantinstructurallyhomologousbacterialisomerases.AlthoughtherelationshipbetweenthecatalyticactivityandBIOLOGicalfunctionofMIFisnotyetfullyunderstood,targetingMIFtautomeraseactivityusingsmall-moleculeinhibitorshasemergedasanattractivestrategyforinhibitingMIFproinflammatoryactivityandattenuatingitsbiologicalactivityinvitroandinvivo.HumanandmouseMIFsharea90%homology.ProductDetails

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