试剂盒提取详细步骤Word格式.docx
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试剂盒提取详细步骤Word格式.docx
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2.Add2.5mlofBeadSolutiontotheBeadTubeandvortextomix.RTCrpUDGiT
2、加2.5mlBeadSolution到磁珠管中并漩涡混合。
3.Add0.25mlofSolutionSR1totheBeadTubeandvortextomix.5PCzVD7HxA
What’shappening:
TheBeadSolutionisabufferusedtodispersecellsandsoilparticles.SolutionSR1containsSDSandotherdisruptionagentswhichaidincompletecelllysis.Inadditiontoaidingincelllysis,SDSisananionicdetergentthatbreaksdownfattyacidsandlipidsassociatedwiththecellmembraneofseveralorganisms.Note:
Ifitgetscold,itwillformawhiteprecipitate.Heatingto60º
CwilldissolvetheSDSandwillnotharmtheotherdisruptionagents.jLBHrnAILg
3、加0.25mlSR1到磁珠管并漩涡混合。
发生的反应:
BeadSolution是一种缓冲液可用来打散细胞和土壤颗粒。
SR1包括SDS和其他的能帮助细胞裂解的破碎剂。
除了帮助细胞破碎外,SDS是阴离子洗涤剂,可以破坏脂肪酸和几种微生物细胞膜相关的脂类。
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如果天气冷了,可能会形成白色沉淀。
加热到60℃溶解SDS,且不会影响其他裂解试剂的作用。
4.Add0.8mlofSolutionSR2andplacetheBeadTubeontheVortexAdapter(MOBIOCatalog#13000-V1-15forVortexGenie2or13000-LV2-15forLabnetVortex>
andvortexatmaximumspeedfor5minutes.LDAYtRyKfE
SolutionSR2isaprecipitationreagentusedtoremovenon-DNAorganicandinorganicmaterialincludinghumicsubstances,celldebris,andproteins.ContaminatingorganicandinorganicmattermayreduceDNApurityandinhibitdownstreamDNAapplications.Vortexingiscriticalforhomogenizationandcelllysis.Zzz6ZB2Ltk
4、加0.8mlSR2到磁珠管,最大转速旋转5min。
反应:
SR2是一种沉淀试剂,用来去除非DNA有机物和无机物包括腐殖质,细胞碎片以及蛋白质。
污染有机物和无机物质可能会降低DNA纯度和抑制后续的DNA利用。
漩涡对细胞均化和细胞裂解至关重要。
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5.RemovetheBeadTubefromtheVortexAdapterandadd3.5mlofphenol:
chloroform:
isoamylalcohol(pH6.5–8.0,[Usersupplied]>
andvortextomixuntilthebiphasiclayerdisappears.rqyn14ZNXI
5、加3.5ml酚/氯仿/异戊醇<
pH6.5-8.0),漩涡混合直到分层消失。
6.PlacetheBeadTubeontheVortexAdapterandvortexatmaximumspeedfor10minutes.EmxvxOtOco
最大转速漩涡混合10min。
Cellsarelysedbycombinationofchemicalagentsfromsteps1-5andthemechanicalshakingintroducedbyvortexing.Phenol:
chloroform:
Isoamylalcoholisaddedtomaximizelysingefficiencyandyield.Lysedcellcomponentsaretrappedinthesolventandproteinsaredenaturedleavingthenucleicacidinsolution.SixE2yXPq5
从1到5步的化学试剂和漩涡混合使细胞裂解,酚/氯仿/异戊醇使其最大程度裂解。
溶解的细胞和试剂混合在一起,蛋白质降解只剩下核酸在溶液中。
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TheMOBIOVortexAdapterisdesignedtobeasimplecosteffectiveplatformtofacilitatethekavU42VRUs
homogenizationandcelllysisofsamples.AnalternativetotheMOBIOVortexAdapterwouldbetoattachyourtubestoyourplatformwithtape.Notethattapecanbecomelooseandmayresultinunevenshakingandlysisefficiencyresultingininconsistentresultsorloweryields.y6v3ALoS89
7.RemovetheBeadTubefromtheVortexAdapterandcentrifugeat2500xgfor10minutesatroomtemperature.M2ub6vSTnP
Centrifugationresultsinphaseseparationofthesamplemixture.Threephaseswillbevisibleaftercentrifugation.Thelowerorganicphasecontainingproteinsandcellulardebris,theinterphasecontaininghumicsandotherorganicandnon-organicmaterial,andtheupperaqueousphasecontainingtotalnucleicacid.Note:
Thethicknessoftheinterphasewilldependonthesampletype.Sampleshighinorganiccontentwillhaveathickerinterphase.0YujCfmUCw
7、室温2500g离心10min。
离心导致混合样品相分离。
离心后能观察到三相,底下的有机相包括蛋白质和细胞碎片,中间相包括腐殖质和其他有机及无机物质,上层相包括所有的核酸。
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中间相的厚度和样品类型有关,样品有机物含量越高,中间相越厚。
8.RemovetheBeadTubefromthecentrifugeandcarefullytransfertheupperaqueousphase(avoidingtheinterphaseandlowerphenollayer>
toaclean15mlCollectionTube(provided>
.Thethicknessoftheinterphasewillvarydependingonthetypeofsoilused.Discardthephenol:
isoamylalcoholinanapprovedwastereceptacle.Note:
Thebiphasiclayerwillbethickandfirminsoilshighinorganicmatterandmayneedtobepiercedtoremovethebottomphenollayerfordisposal.sQsAEJkW5T
8、小心地移取上层水相到一15ml收集管中。
有机物含量高两相层可能会较厚较坚固,可能需要移取底层的酚相来处理。
Theupperaqueousphasecontainingthetotalnucleicacidsfromthesampleistransferredtoanewtube.Cellulardebris,proteins,andorganicmaterialareleftbehind.Note:
Takecarenottotransfermaterialfromthelowerphaseortheinterphase.GMsIasNXkA
包括样品总核酸上层水相转移到新收集管中。
丢弃细胞碎片,蛋白质和有机物。
不要碰到中间相和下层酚相。
9.Add1.5mlofSolutionSR3totheaqueousphaseandvortextomix.Incubateat4°
Cfor10minutes.TIrRGchYzg
SolutionSR3isasecondaryprecipitationsteptofurtherremoveproteinsandcellulardebris.7EqZcWLZNX
9、加1.5mlSR3到水相中,漩涡混合。
4℃静置10min。
加SR3是二次沉淀步骤,进一步去除其中的蛋白质和细胞碎片。
10.Centrifugeat2500xgfor10minutesatroomtemperature.lzq7IGf02E
10、室温2500g离心10min。
11.Transferthesupernatant,withoutdisturbingthepellet,toanew15mlCollectionTube(provided>
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Thesupernatantcontainingnucleicacidsaretransferredtoanew15mltube.Nonnucleicacidmaterialisleftbehind.NrpoJac3v1
11、将上清液转移到15ml收集管中<
不要碰到下面的沉淀物)。
包括核酸的上清液转移到新的收集管中,剩下非核酸物质。
12.Add5mlofSolutionSR4totheCollectionTubecontainingthesupernatant,invertorvortextomix,andincubateat-20°
Cfor30minutes.1nowfTG4KI
Note:
Forsampleswithhighsaltcontent,incubationinSolutionSR4atroomtemperaturewillresultinhigherRNAyields.fjnFLDa5Zo
12、加5mlSR4到收集管中,倒置混合,-20℃静置30min。
对于含盐量高的样品,室温条件下加SR4静置将得到高RNA产量。
13.Centrifugeat2500xgfor30minutesatroomtemperature.tfnNhnE6e5
13.、室温2500g离心30min。
14.Decantthesupernatantandinvertthe15mlCollectionTubeonapapertowelfor5minutes.HbmVN777sL
Dependingonsoiltype,thepelletmaybelargeand/ordarkincolor.V7l4jRB8Hs
SolutionSR4is100%Isopropanol.NucleicacidisprecipitatedandtheIsopropanolisdiscarded.83lcPA59W9
14、倒出上清液,将收集管倒置在纸巾上5min。
依据土壤类型的不同,沉淀可能较大或颜色上较深。
SR4是纯异戊醇。
沉淀核酸,丢弃上清液。
15.ShakeSolutionSR5tomix.Add1mlofSolutionSR5tothe15mlCollectionTubeandresuspendthepelletcompletely.(Note:
Dependingonthesoiltype,thepelletmaybedifficulttoresuspend.Resuspensionmaybeaidedbyplacingthetubesinaheatblockorwaterbathat45°
Cfor10minutes,followedbyvortexing.Repeatuntilthepelletisresuspended.>
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SolutionSR5isaproprietarysaltsolutionusedtoresuspendtheprecipitatednucleicacidsfromstep14.ItisalsousedtoequilibratetheRNAcapturecolumninstep16andtowashandprepthecolumnfortheelutionofRNAinstep20below.AVktR43bpw
15、摇晃SR5使其混合,加1mlSR5到收集管中,使沉淀再完全悬浮。
土壤样品不同,沉淀有可能不易悬浮,可能需要将收集管放到45℃的水浴池中10min再悬浮,再漩涡混合,重复这样直到沉淀重悬浮。
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16.PrepareoneRNACaptureColumn(provided>
foreachRNAIsolationSample:
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a.Removethecapofa15mlCollectionTube(provided>
andplacetheRNACaptureColumninsidethe15mlCollectionTube.Thecolumnwillhanginthe15mlCollectionTube.gIiSpiue7A
b.Add2mlofSolutionSR5totheRNACaptureColumnandallowittogravityflowuEh0U1Yfmh
throughthecolumnandcollectinthe15mlCollectionTube.AllowSolutionSR5toIAg9qLsgBX
completelyflowthroughthecolumn(Optional:
TheCollectionTubemaybeemptiedafterSolutionSR5hascompletelyflowedthroughthecolumn.Note:
DONOTALLOWTHECOLUMNTODRYOUTPRIORTOLOADINGTHERNAISOLATIONSAMPLE.>
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16、为每个RNA样品准备一个捕集柱。
a.将捕集柱悬挂到收集管上。
b.加2mlSR5到捕集柱上,使其重力流。
允许SR5完全流过捕集柱。
在加RNA样品前不要让捕集柱流干。
17.AddtheRNAIsolationSamplefromStep15ontotheRNACaptureColumnandallowittogravityflowthroughthecolumn.Collecttheflowthroughinthe15mlCollectionTube.asfpsfpi4k
17、将15步的RNA分离样加到捕集柱中,使其流过捕集柱。
18.Washthecolumnwith1mlofSolutionSR5.Allowittogravityflowandcollecttheflowthroughinthe15mlCollectionTube.ooeyYZTjj1
ThesampleisaddedtotheRNACaptureColumnandthenucleicacidsareboundtothecolumnmatrix.TheCaptureColumnisthenwashedwithasecondvolumeofSolutionSR5toensureunboundcontaminantsareremovedfromthesampleandcolumnpriortotheelutionofRNA.BkeGuInkxI
18、用1mlSR5洗涤捕集柱,流出液收集在收集管中。
样品加到捕集柱上,核酸结合到柱基质上。
捕集柱用SR5洗涤确保没结合的污染物被去除掉。
19.TransfertheRNACaptureColumntoanew15mlCollectionTube(provided>
.ShakeSolutionSR6andthenadd1mlofSolutionSR6totheRNACaptureColumntoelutetheboundRNAintothe15mlCollectionTube.AllowSolutionSR6togravityflowintothe15mlCollectionTube.PgdO0sRlMo
TheSolutionSR6RNAelutionbufferisaproprietarysaltsolutionthatallowsforthepreferentialreleaseofRNAfromtheRNACaptureColumnleavingDNA,residualdebris,andinhibitingsubstancesinthecolumn.Note:
anewkitisavailableforDNAelution.SeeDNAElutionProcedureintheHintsandTroubleshootingGuideorcontactMOBIOfordetailsattechnical@3cdXwckm15
19、将捕集柱转移到新收集管中,摇晃SR6,然后加1mlSR6到捕集柱中使其流过捕集柱,洗提RNA。
SR6RNA洗提缓冲液是专有的盐溶液,它能使RNA流出而DNA、剩下的细胞碎片和抑制剂依然留在捕集柱上。
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20.TransfertheelutedRNAtoa2.2mlCollectionTube(provided>
andadd1mlofSolutionSR4.Invertatleastoncetomixandincubateat-20°
Cfor10minutes.v4bdyGious
20、将洗提的RNA转移到2.2ml的收集管中,并加1mlSR4,至少倒置混合一次,-20℃静置10min。
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21.Centrifugethe2.2mlCollectionTubeat13,000xgfor15minutesatroomtemperatureto
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