Kitsize | 96 |
Method | ELISA |
Incubationtime | 1x3h,1x1h,1x15min |
Standardrange | 10-250ng/mL |
Specimen/Volumes | 50µLserum,plasma,cellculturesupernatant |
Substrate/isotope | TMB450nm |
RegulatoryStatus: | Forresearchuseonly |
Aggrecan(PG)isthepredominantproteoglycanspeciesinarticularcartilage.Itiscomposedofacoreproteinof210kDatowhichover100chondroitinsulfatechains,about20-50keratansulfatechainsandO-linkedaswellasN-linkedoligosaccharidesarecoventlyattached.
Thecoreproteincontainsthreedistinctglobulardomains(G1-G3).G1isattheaminoterminus,separatedbyashortextendedsegmentfromG2,whileG3isatthecarboxyterminalend.TheG1aminoterminalregioncaninteractnoncovalentlywithhyaluronicacid(HA)andhasthenbetermedthehyaluronicacidbindingregion(HABR).AlinkproteininteractwithboththeG1regionandtheHAtostABIlizethisinteraction.PGisproducedbychondrocytes,anditsproductionisregulatedbycytokinesandgrowthfactorssuchasIL1β,TNFα,IGF1orTGFβ.Inextracellularmatrix,asmanyas200aggrecanmoleculescanbindtoonesingleHAmoleculetoformanaggregate(MW:5107to5108).
Animbalanceinthesynthesisanddegradationofthematrixcomponentsisacommonfeatureofbothosteoarthritisandrheumatoidarthritis.ThelossofPGandothermatrixcomponentsfromthecartilageleadstodestructionofthetissue,causingcompletedeteriorationofthearticularsurface.SeveralrecentpublicationssuggestthatthePGandPGfragmentsreleasedinsynovialfluidandserumduringthedegradationprocessmightserveasMarkersofmetabolicchangesindiseasedcartilage.Cellcultureisacommonlyusedprocedureforthestudyofcartilagemetabolism.ThemeasurementofPGandothermatrixcomponentsinculturesupernatantsandcellularcontentscanassisttheanalysisofofcytokine,growthfactor,drugandpotentialchondroprotectivesubstanceeffectsonthecartilagehomeostasis.IBLInternationalsellsthisELISAforthemeasurementofhumanaggrecantoaidthestudyofthisimportantcartilageconstituent.TheAggrecan/PGELISAisconvenient,highlyspecific,andallowsaccuratemeasurementofPGinsynovialfluid,serumandculturesupernatant.
Thisassayisaninterestingtoolfortheexplorationofthecartilagemetabolism.