Diapharma/TECO®超敏感鲤鱼卵黄原蛋白ELISA/TE1046/Kit/96试验

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货号:TE1046
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品牌:Diapharma
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Description:

TheTECO®UltraSensitiveCyprinidVitellogeninELISA kitisaverysensitiveenzymelinkedimmunosorbentassayforthequantitativedeterminationofvitellogenin(VTG)incyprinidfishmucusorcellculture*.

Cyprinid Vitellogenin ELISA, Perch (Perciformes) Vitellogenin ELISA

VitellogenindeterminationisoneofthecoreendpointsinscreeningandtestingforendocrinedisruptingchemicalsstandardizedintheOECDGuidlinesforthetestingofchemicalsforestrogenicactivity:

  •  OECD(2009),TestNo.229
  •  OECD(2009),TestNo.230
  •  OECD(2011),TestNo.234

Vitellogenindeterminationisusedinecotoxicologicalstudiestodeterminetheeffectsofestrogeniccompoundsinthewater.

AssayMeasuringRange: 0-2.0ng/ml

AssaySensitivity: <0.03ng/ml

Incubationtime:Overnight16-24hours/4h±10min

SampleVolume: 50µl

SamplePreparation:

  • Mucus: CollectasdescribedintheTECO®MucusCollectionSet(TE1034).Mucuscontainingswabscanbestoredseveralmonthsat<-20°C.
  • Cellculture:Storefreshsamplesimmediatelyaftercollectionat<-20°Cuntilassayed.

ReferenceValues:

  • Mucuslevelsareintherangeofng/ml.

*Additionalassayvalidationmayberequiredwiththeuseofcellculturesamples.

KitComposition:

KitContents:

  • AntibodyCoatedMicroassayPlate: 96-wellplate (12×8break-apartwellstripscoatedwithIgGdirectedagainstCyprinidVTG)
  • StandardStockSolution:35ng,2vials
  • ControlC1:  lowcontrol,2vials
  • ControlC2:high control,2vials
  • WashBuffer: 1x30ml,50X.Dilute1:50withdeionizedwater.
  • DilutionBuffer:1x55ml.Readytouse.
  • MatrixSolution:1x7ml.Readytouse.
  • BiotinylatedAntibody(Biotin-AB):1x12ml.Readytouse.
  • StreptavidinPeroxidaseConjugate(SA-HRPConj.):1x12ml. Readytouse.
  • TMBSubstrate:1x12ml. Readytouse.
  • StopSolution: 1x12ml 1MHCl.Readytouse.

Materialsrequiredbut notsupplied:

Pipettes,10μl–1000μl
•Multichannelpipettes,50μl–100μl
•Graduatedcylindersforreconstitutingand dilutingreagents
•ManualAspirationSystemorautomaticwasherforELISAplates
•Distilledwater
•Vortexmixer
•ELISAplatereadersuitablefor96wellformatsandcapableofmeasuringat450nm(Reference:590-650nm).
Forextendedstandardrange:ELISAplatereadersuitablefor96wellformatsandcapableofmeasuringat 405nmand450nm(Reference:590-650nm)
•ELISAplateshaker(500rpm)
•Softwarepackagefordatagenerationandanalysis

Formucussamples:TheMucusCollectionSet(TE1034)whichincludesExtractionBufferandvalidatedSamplingSwabsis alsorequired.

AssayPrinciple:

AssayPrinciple

TheTECO®UltraSensitiveCyprinidVitellogeninELISA kitisa96wellimmuno-captureELISAproduct.Samplesareincubatedwiththevitellogeninspecificantibodycoatedmicrotiterplate.Afterunboundmaterialiswashedout,apolyclonalbiotinylatedantibodybindstothevitellogenin.Inthefollowingincubationstep,astreptavidin-peroxidaseconjugatebindstothebiotinylatedantibody.Inthefinalsubstratereaction,thecolordevelopmentisdirectlyproportionaltotheamountofvitellogenininthesample.

ResultAnalysis

Thestandardrangeoftheassayisbetween0.025and2.0ng/ml.Acalibrationcurvecanbeestablishedbyplottingstandardconcentrationonthex-axis(linearscale)againsttheabsorbanceofthestandardsonthey-axis(linearscale).Thevitellogeninconcentrationscanthenbereadoffthecalibrationcurve. A4-parametercurvefitshouldbeusedforautomaticdatareduction.Ifsampleswerepre-diluted,theconcentrationwillbeobtainedbymultiplyingthevaluereadoffthecalibrationcurvebythedilutionfactor.Notethatthedilutioncorrectionformucusisnotnecessaryifonlythe0.5mlExtractionBufferwasaddedtotheswab.SampleswithhigherabsorbancevaluesthanStandardAshouldbere-testedafterdilutingwithDilutionBufferandthenthis additionaldilutionshould betakeninaccountfortheconcentrationcalculation.

Ultra Sensitive Cyprinid VTG ELISA Standard Curve

TECO®UltraSensitiveCyprinidVTGELISAStandardCurveExample

Species:

  • Carp(Cyprinuscarpio)
  • Goldfish(Carassiusgibelioauratus)
  • Zebrafish(Daniorerio)
  • Fatheadminnow(Pimephalespromelas)
  • Commonbream/freshwaterbream/bronzebream/carpbream(Abramisbrama)
  • Roach(Rutilusrutilus)
  • Commonrudd (Scardiniuserythrophthalmus)
  • Chub(Squaliuscephalus)
  • Commonnase (Chondrostomanasus)
  • Bleak(Alburnusalburnus)
  • NeonTetra(Paracheirodoninnesi)
  • Gudgeon(Gobiogobio)
  • Commondace(Leuciscusleuciscus)
  • Stoneloach(Barbatulabarbatula)
  • Commonminnow(Phoxinusphoxinus)

Background:

Inoviparousanimals,vitellogenin(VTG)isanestrogen-inducedyolkprecursorproteinmainlysynthesizedinthelivertobedepositedinthematuringoocytes,whereitissplitintheyolkproteinslipovitellin1,lipovitellin2andphosvitin.Theseyolkproteinsserveasnourishmentstorageforthedevelopingembryos.Non-physiologicalinductionofvitellogenininmalesorinjuvenilefishisthoughttoindicateanestrogenmediatedendocrinedisruption.Therefore,VTGdeterminationisoneofthecoreendpointsinscreeningandtestingforendocrinedisruptingchemicalsstandardizedintheOECDGuidelinesforthetestingofchemicalsforestrogenicactivity.Normally,vitellogeninismeasuredinbloodsamplesorwholebodyhomogenate(WBH)–butbothsampletypesrequireinvasiveanddestructivetreatmentofthefish.Bloodcanbe difficulttocollect,inparticularwhereverysmallfishareconcernedand wheretheanimalsmustsurvivesampling.

Recently,severalcelltypeshavebeenshowntoproduceVTGafterestrogenstimulation,includingthoseoftheepidermalmucosa.EventhoughtheVTGconcentrationintheskinmucusisanorderofmagnitudelowerthaninbloodserumorinbodyhomogenates(containinglivertissue),theskinmucosaisverywellsuitedasamatrixfor determiningexogenousVTGinductioncausedbyenvironmentalchemicalswithaffinitytoestrogenreceptors.ByusingahighlysensitiveELISAincombinationwithauniquesamplingandextractionsystemthedeterminationofmucosa-bornVTGdeterminationhasthefollowingadvantages:

  • Simpleandhighlystandardizedsamplingtechniqueandsamplepreparation.
  • Strictlydefinedmatrixwithoutproteasecontaminationcausedbynon-targettissuesorlymphaticfluid.
  • Non-destructiveandtherebyallowingseveralsubsequentsamplingsinordertorecordakineticofVTGinductionwithamaximumknowntoappearafter7daysofexposure.ThereforeMucosatestarefullycompatIBLewithacuteaswellaschronicalOECDtestmethods.
  • Epithelialorganizedepidermisisdirectlyexposedtoexogenousestrogensandtherebyallowingadirectcomparisonwithinvitrotestusingestrogensensitivevitellogeninproducingfishcelllines.
  • LowerdegreeofinterferencewithendogenousVTGproduction(infemales)andbioconcentrationorenterohepaticcirculationoftheeffectiveestrogen(xenoestrogen)andtherebyshowingacleardoseresponserelationship.
  • StABIlityofstandardsandsamplesifprescribedstorageconditionsareobserved.

The TECO®UltraSensitiveCyprinidVitellogeninELISA kitprovidesahigh-sensitivityELISAoptionforresearchersdeterminingVTGproteinconcentrationinfishmucusorcellculturesamples.

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