IBL/IGF-II ELISA/MD58041/
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产品分类:
夹心法ELISA
公司分类:
Sandwich_method_ELISA
联系Q Q:
3392242852
电话号码:
4000-520-616
电子邮箱:
info@ebiomall.com
商品介绍
Kitsize | 12x8 |
Method | ELISA |
Incubationtime | 1x2h,1x30min,1x30min |
Standardrange | 0,016-3.609µg/L |
Specimen/Volumes | 5µLSerum,Plasma |
Substrate/isotope | TMB,450nm |
RegulatoryStatus: | EU:CE |
Detailsfor: IGF-IIELISA
TheIGF-IIELISAiscalibratedagainsttheInternationalStandard:WHONIBSC96/538.
ThestandardsoftheELISAarehumanIGF-IIinconcentrations0.45;1.5;3;5.63and9ng/ml,respectivelytheassayrangecovers–atrecommendednormalsampledilution-therangeto2400ng/ml.Byvaryingthesampledilutionthiscanbeadaptedtothespecialindividualrequirements.
Sensitivity
TheanalyticalsensitivityoftheELISAyields0.02ng/ml(2SDofzerostandardin20folddetermination).
TheInter-andIntra-Assayvariationcoefficientsarelessthan7.2%and6.6%respectively.
INTENDEDUSE
Scientificinvestigationsinthefieldofneonatalhypertrophy(IGF-IIisafoetalgrowthfactor)andmalignancies(IGF-IIisamonogenicgrowthfactor).
IGF-IIseemstobeofuseindifferentialdiagnosticsofmalignancies.Thus,itispossIBLetodifferentiatebyIGF-IIbetweenadrenocorticalcarcinomasandadenomas.FurthertumorstaginganddifferentiationbetweenhyperplasiaandcarcinomacanbeimprovedbyIGF-IImeasurementsinprostatetumors.TheIGF-Systemseemtobeofrelevanceinneurodegenerationaswell,e.g.Alzheimer´sandParkinson’sdiseases.
Theinsulin-likegrowthfactors(IGF)-Iand–IIplayapivotalroleintheregulationofproliferationanddifferentiationofseveraltissuetypes.IGF-IalsocalledSomatomedinChasamolecularweightof7.469kDa.ItsexpressionismainlyregulatedbyGrowthHormoneandnutrition.ButseveralhormonesandpeptidefactorsareknowntoinfluenceIGF-IIsynthesisindifferenttissues.BioavailABIlityoftheIGFsisregulatedbyspecificbindingproteins(IGFBP).BesidethehighaffinityInsulin-likeGrowthFactorBindingProteins1-6,IGFsarealsoboundbeIGFBP-relatedProteins.ThesebindingproteinsbindIGF-IandIGF-IIwiththesameaffinityorpreferIGF-II.DirectmeasurementofIGFsinserumsampleswithoutpretreatmentresultsinfalsevaluesbecauseoftheextremelyslowdissociationoftheIGF/IGFBPcomplexesduringtheassayincubationonlyapartoftheIGF-IIinthespecimencanbindtotheantibodiesandbedetected.
Therefore,varioustechniqueswereappliedtophysicallyseparateIGF-IIfromitsbindingproteinsbeforemeasurement,including(a)sizeexclusionchromatographyunderacidicconditions,(b)solid-phaseextractionand(c)acid-ethanolextraction.Thesetechniques,however,areeitherinconvenientortime-consumingorgiveincompleteandnot-reproduciblerecoveries.
Thisassayiseasy,fastandresultsdonotdependonthebindingproteinconcentrationofthesample.ItisbasedonthehighspecificityoftheemployedantibodiesforIGF-II.Thereisvirtuallynocross-reactivitywithIGF-I.ThisallowstheseparationofIGF-IIfromthebindingproteinsbyacidificationandblockingofthefreebindingproteinswithIGF-I.Thus,theendogenousIGF-IIisfreeinsolution.
ForconcretedatapleaseconsulttheInstructionforUseinthedownloadboxontherightside.ThestandardsoftheELISAarehumanIGF-IIinconcentrations0.45;1.5;3;5.63and9ng/ml,respectivelytheassayrangecovers–atrecommendednormalsampledilution-therangeto2400ng/ml.Byvaryingthesampledilutionthiscanbeadaptedtothespecialindividualrequirements.
Sensitivity
TheanalyticalsensitivityoftheELISAyields0.02ng/ml(2SDofzerostandardin20folddetermination).
TheInter-andIntra-Assayvariationcoefficientsarelessthan7.2%and6.6%respectively.
INTENDEDUSE
Scientificinvestigationsinthefieldofneonatalhypertrophy(IGF-IIisafoetalgrowthfactor)andmalignancies(IGF-IIisamonogenicgrowthfactor).
IGF-IIseemstobeofuseindifferentialdiagnosticsofmalignancies.Thus,itispossIBLetodifferentiatebyIGF-IIbetweenadrenocorticalcarcinomasandadenomas.FurthertumorstaginganddifferentiationbetweenhyperplasiaandcarcinomacanbeimprovedbyIGF-IImeasurementsinprostatetumors.TheIGF-Systemseemtobeofrelevanceinneurodegenerationaswell,e.g.Alzheimer´sandParkinson’sdiseases.
Theinsulin-likegrowthfactors(IGF)-Iand–IIplayapivotalroleintheregulationofproliferationanddifferentiationofseveraltissuetypes.IGF-IalsocalledSomatomedinChasamolecularweightof7.469kDa.ItsexpressionismainlyregulatedbyGrowthHormoneandnutrition.ButseveralhormonesandpeptidefactorsareknowntoinfluenceIGF-IIsynthesisindifferenttissues.BioavailABIlityoftheIGFsisregulatedbyspecificbindingproteins(IGFBP).BesidethehighaffinityInsulin-likeGrowthFactorBindingProteins1-6,IGFsarealsoboundbeIGFBP-relatedProteins.ThesebindingproteinsbindIGF-IandIGF-IIwiththesameaffinityorpreferIGF-II.DirectmeasurementofIGFsinserumsampleswithoutpretreatmentresultsinfalsevaluesbecauseoftheextremelyslowdissociationoftheIGF/IGFBPcomplexesduringtheassayincubationonlyapartoftheIGF-IIinthespecimencanbindtotheantibodiesandbedetected.
Therefore,varioustechniqueswereappliedtophysicallyseparateIGF-IIfromitsbindingproteinsbeforemeasurement,including(a)sizeexclusionchromatographyunderacidicconditions,(b)solid-phaseextractionand(c)acid-ethanolextraction.Thesetechniques,however,areeitherinconvenientortime-consumingorgiveincompleteandnot-reproduciblerecoveries.
Thisassayiseasy,fastandresultsdonotdependonthebindingproteinconcentrationofthesample.ItisbasedonthehighspecificityoftheemployedantibodiesforIGF-II.Thereisvirtuallynocross-reactivitywithIGF-I.ThisallowstheseparationofIGF-IIfromthebindingproteinsbyacidificationandblockingofthefreebindingproteinswithIGF-I.Thus,theendogenousIGF-IIisfreeinsolution.
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