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Human Peripheral Blood Mononuclear Cell Preparation
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================ 蚂蚁淘在线 ================ 免责声明:本文仅代表作者个人观点,与本网无关。其创作性以及文中陈述文字和内容未经本站证实,对本文以及其中全部或者部分内容、文字的真实性、完整性、及时性本站不做任何保证或承诺,请读者仅作参考,并请自行核实相关内容 版权声明:未经蚂蚁淘在线授权不得转载、摘编或利用其他方式使用上述作品。已经经本网授权使用作品的,应该授权范围内使用,并注明“来源:蚂蚁淘在线”。违反上述声明者,本网将追究其相关法律责任。 Procedure1.Pourbuffycoat(seeHint#1)fromthebagintoa125mlconicalpolypropylenecentrifugetubeanddiluteto90mlwithsterileendotoxin-freePBS.2.Add15mlofsterileDextran/PBSandmixbyinvertingthetubefourtofivetimes.Ifanybubblesappear,theyshouldberemovedwitha1mlplasticPipette(seeHint#2).3.Leavethemixtureundisturbedatroomtemperaturefor20mintoallowtheerythrocytestosediment.4.TransferthesupernatantwithaplasticpipettetoafreshtubeandaddanequalvolumeofPBS/EDTA.5.Centrifugeat1,000Xgfor10minatroomtemperaturetopellettheleukocytes,leavingtheplateletsinsUSPension.6.Pourthesupernatantintoacontainerofbleach(seeHint#1),resuspendthecellpelletin1to2mlofPBS,andtransferthelattertoafreshtube(toavoidcontaminatingthesolutionwiththeplateletsthatareadheringtothesidesofthetube).7.Bringthecellsuspensiontoafinalvolumeof50mlandgentlyoverlay12.5mlontotheFicoll-Hypaqueinfour50mlconicaltubes(15mlFicoll-Hypaquepertube).8.Centrifugeat800Xgfor20minat12°CwiththeBRAKEOFF.9.ThemononuclearleukocytesshouldappearasacloudyringatthePBS/Ficollinterface.Harvestthemfromtheinterfacewitha2or5mlpipette.10.Transferthecellsfromeachinterfacetoafresh50mltubeandfillwithPBS.11.Centrifugethesuspensionat800Xgforaminimumof10mintopelletthecells.Aspiratethesupernatantandresuspendthecellpelletsinappropriatebuffer(seeHint#3). Solutions PBS/EDTA 4.3mMSodiumPhosphate,Dibasic(Na2HPO4)pH7.22.7mMKCl1.8mMPotassiumPhosphate,Monobasic(KH2PO4)5mMEDTA137mMNaCl ![]()
PBS 4.3mMSodiumPhosphate,Dibasic(Na2HPO4)pH7.22.7mMKCl1.8mMPotassiumPhosphate,Monobasic(KH2PO4)AlsoseeProtocol#2152137mMNaCl ![]()
Ficoll-Hypaque1077 Incubate15mlinfour50mltubesMustbeatroomtemperatureEquilibratetoroomtemperature ![]()
Dextran/PBS 6%(w/v)DextranT500(Pharmacia)PrepareinsterilePBS(Ca2+,Mg2+free) ![]()
BioReagentsandChemicals 1.CAUTION!Thissubstanceisabiohazard.Consultthisagent"sMSDSandinstitutionalpoliciesforproperhandlinginstructionsforhumanblood.2.Thebubblestrapredbloodcells.3.Todepletemonocytes,culturethemononuclearcellmixtureinseveral10cmdishesfor30minutesto1hour.Monocytesadheretotheplasticdishandthenonadherentlymphocytescanbetransferredtoanewtube. 相关普通细胞培养
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