外泌体研究

Signosis/ApoptosisAssociated miRNA Plate Array/MA1002/1 Ea

Description:

Apoptosisinvolvesaseriesofbiochemicaleventsleadingtoacharacteristiccellmorphologyanddeath,includingchangestothecellmembrane,cellshrinkage,nuclearfragmentation,chromatincondensation,andchromosomalDNAfragmentation.Itplaysimportantrolesinremovingunwantedcellsduringdevelopmentandhomeostasis.Excessiveapoptosiscauseshypotrophy,suchasinischemicdamage,whereasaninsufficientamountresultsinuncontrolledcellproliferation,suchascancer.MicroRNAsarenewlydiscoveredsmallnon-codingRNAmoleculesthatregulateupto30%ofmammaliangeneexpression.NumerousmiRNAshavebeenrevealedtohaveaninfluenceontheregulationofapoptoticcellsignalingsuchasoverexpressionofmiR-145,miR-216,miR-182,andmiR-96miRNAtodecreasecaspase-3activation.SignosisdevelopedamiRNAarrayfortargeting47miRNAsthathavebeenshowninliteraturetobeinvolvedinapoptosis.ProfilingtheexpressionofthesemiRNAswillfacilitateinuncoveringtheregulationofmiRNAinapoptosis.

ApplicableGrid:

 ListofApplicablemiRNAs

 123456789101112
ALet-7a-5pmiR-16-5pmiR-142miR-155-5pmiR-202-5pmiR-337Let-7a-5pmiR-16-5pmiR-142miR-155-5pmiR-202-5pmiR-337
BLet-7b-5pmiR-21-5pmiR-144miR-182-5pmiR-204-5pmiR-338Let-7b-5pmiR-21-5pmiR-144miR-182-5pmiR-204-5pmiR-338
CLet-7c-5pmiR-24-3pmiR-145-5pmiR-184miR-210-3pmiR-345Let-7c-5pmiR-24-3pmiR-145-5pmiR-184miR-210-3pmiR-345
DmiR-1miR-25-3pmiR-148miR-188-5pmiR-214-3pmir-376c-3pmiR-1miR-25-3pmiR-148miR-188-5pmiR-214-3pmir-376c-3p
EmiR-7-5pmiR-26miR-150-5pmiR-193amiR-216-5pmiR-369-5pmiR-7-5pmiR-26miR-150-5pmiR-193amiR-216-5pmiR-369-5p
FmiR-10a-5pmiR-96miR-151-3pmiR-193bmiR-218-5pmiR-369-3pmiR-10a-5pmiR-96miR-151-3pmiR-193bmiR-218-5pmiR-369-3p
GmiR-15a-5pmiR-101miR-152miR-196a-5pmiR-224-5pmiR-371miR-15a-5pmiR-101miR-152miR-196a-5pmiR-224-5pmiR-371
HmiR-15b-5pmiR-133bmiR-153-3pmiR-197-3pmiR-296-5pU6miR-15b-5pmiR-133bmiR-153-3pmiR-197-3pmiR-296-5pU6

Principle:

Signosis’miRNAdirecthybridizationplatearrayisasimpletwo-stepassay;platehybridizationandstreptavidin-HRPdetection.Theplateispre-coatedwithanoligomix,includingapairofuniqueoligosthathybridizeside-by-sidetoaspecifictargetmiRNAandauniversalcaptureoligoandabiotin-labeledoligo.Intheassay,totalRNAisdirectlyutilizedforhybridization.WhenthetargetmiRNAexistsinRNA,itactsasabridgetobringthebiotin-labeledoligotothecaptureoligo,whichcanbedetectedthroughstreptavidin-HRPconjugateandachemiluminescentsubstrate.IfthereexistsnospecificmiRNA,thebiotin-labeledprobewillbewashedaway,leadingtonodetection.Intheplatearray,48wellsarecoatedwithdifferentoligomixesfordifferentmiRNAs.Asingle96-wellplateallowsquantitativemeasurementandcomparisonof48miRNAsbetweentwosamples.U6RNAisusedfornormalization.

Data:



Apoptosis-associatedmiRNAplatearrayusedforanalyzingtheexpressionof48miRNAsinhumanHEK293adnU937totalRNAs.

 
 

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