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主营:血管内皮生长因子-C, Spp1, IRF-3, DPYSL2, GLUT5
℡ 4000-520-616
℡ 4000-520-616
IBL/IGF-1 direct (Rat, Mouse) ELISA/30117393/
产品编号:30117393
市  场 价:¥0.00
场      地:美国(厂家直采)
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:待定
品      牌: IBL
公      司:IBL,inc
公司分类:
IBL/IGF-1 direct (Rat, Mouse) ELISA/30117393/
商品介绍
Kitsize12x8
MethodELISA
Incubationtime1x1h,1x30min,1x30min
Standardrange0.5-18µg/L,AssayRange:0.029-180µg/L
Specimen/Volumes5µLserum,plasma/withoutextraction
Substrate/isotopeTMB450nm
RegulatoryStatus:Forresearchuseonly
Detailsfor: IGF-1direct(Rat,Mouse)ELISA
Mouse/RatIGF-IELISA
  • issuitedforIGF-Ideterminationinserumandplasmaofmiceandrats
  • highsensitive:0.029ng/mlanalyticalsensitivity;requiredsamplevolumeisverysmall
  • isfast:incubationtimeatotalof2hours
  • SingleStandardswith0.5,2.5,6,12,18ng/mlrecombinantIGF-IareprovidedintheKit
  • 2ControlSeraareprovidedforqualitycontrol
  • useshighaffinityantibodiesagainstm/rIGF-I
  • Microtiterplatesareseparatelybreakapart

IntendedUse

MeasurementofIGF-Iinmouse/ratserumandplasma.

INTRODUCTION

Besidedifferentcellculturemodelsandstudieswithhumanpatients,miceandratsaresuitablemodelorganismsforbasicresearchandpre-clinicalstudies.Thus,wedevelopedthistestsystemasatoolforIGF-Imeasurementsinmiceandratforusageinresearchandpreclinicalstudies.EvenifthecomparABIlityofmiceandhumansislimitedweoffersomebackgroundinformationonthehumanIGF-Isysteminthefollowingsection:

Insulin-likegrowthfactors(IGF)IandIIplayapivotalroleinregulatingtheproliferationanddifferentiationofmanycelltypes.IGF-IisidenticalwithSomatomedinC(Sm-C)andhasamolecularweightof7649daltons.Itsmajorregulatorsaregrowthhormone(GH)andnutrition(6).Incontrasttomanyotherpeptidehormones,IGFsareavidlyboundtospecificbindingproteins(IGFBP).ThesevenIGFBPswhichareknownatpresenteitherbindIGF-IandIGF-IIwithsimilaraffinitiesorshowapreferenceforIGF-II.

AmajorproblemofIGF-ImeasurementresultsfromtheinterferenceofIGFBPsintheassay.DirectdeterminationsinuntreatedserumsamplesgivefalsevaluesbecauseoftheextremelyslowdissociationoftheIGF-I/IGFBP-3complexesduringtheassayincubation.DependingontheratioIGF-ItoIGFBPinthesampleinterferencecomesup.

Therefore,varioustechniqueswereappliedtophysicallyseparateIGF-Ifromitsbindingproteinsbeforemeasurement,including(a)sizeexclusionchromatographyunderacidicconditions,(b)solid-phaseextractionand(c)acid-ethanolextraction.Thesetechniques,however,areeitherinconvenientortime-consumingorgiveincompleteandnotreproducIBLerecoveries.Themostwidelyusedmethodistheacid-ethanolextractionwitharecoveryofonly70-80%ofIGFBP-boundIGF-Iasaresultofco-precipitation.Theabsoluteresultsofsuchanextractionarethereforefalselow.TheextractionremovestheIGFBPsonlyinsufficientlyandleadstoreductioninsensitivityoftheassayduetopredilutionofthesamplesbytheextractionprocedure.FurThermore,theremainingIGFBPmaystillinterfereintheassay.Inaddition,theacid-ethanolextractionisineffectiveinspecimensotherthanserumorplasma(e.g.cellculturemedia),inwhichdeterminationofIGF-IisalreadydifficultenoughduetothefactthatIGFBPsarefrequentlypresentatlargeexcess.

Toavoidthesedifficulties,anuncomplicatedassaywasdeveloped,inwhichspecialsamplepreparationisnotrequiredbeforemeasurement.

ForconcretedatapleaseconsulttheInstructionforUseinthedownloadboxontherightside.
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