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Encapsula/Lyophosome™ made from Diether Lipids/10-mg/LDE-501
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liposomesareextensivelyusedtostudytheinteractionofproteins,peptidesandothermoleculeswiththesurfaceofalipidmembrane.OneoftheparametersthataffectsthisinteractionisthechargeoftheLiposomalmembrane.Liposomesarealwaysmadeinaqueousenvironmentandtheyaresizedtothedesiredsizeinliquidstateusingvariousmethodssuchashigh-pressureextrusionthroughnanosizedporetracketchmembranes.Liposomewithoutwaterismeaningless.Inrareoccasions,liposomesarefreezedriedandproliposomesareformedinthepresenceofalyoprotectantsuchastrehalose.Usingalyoprotectantisnecessaryinordertomaintainthesizeoftheliposomesafterrehydration.Thefundamentalstructureofcellmembranesisbilayerscomposedofphospholipids,andthevitalfunctionofthephospholipidsinthemembraneistohelpkeepitfluidandsemi-permeable.Conventionalglycerophospholipidshaveacylchainsattachedtothesn-1andsn-2positionsoftheglycerolbackboneviaanesterbond.Etherlipidsareauniqueclassofglycerophospholipidsthathaveanalkylchainattachedtothesn-1positionbyanetherbond(glycerol-etherlipids). Inetherlipids,thealcoholgroupattachedtothephosphateisgenerallycholineorethanolamine.Ether-linkedphospholipidssuchas1-alkyl-2-acyl-phosphatidylcholineanddialkylphosphatidylcholinearealsofoundintheplasmaandorganellemembranesofmammalianspecies.Etherlipidsformapproximately20%ofthetotalphospholipidinmammalswithdifferenttissuedistribution;brain,heart,spleenandwhitebloodcellshavethehighestlevels,whileliverhaveaverylittleamountofetherlipids.StudiesontheformationandThermodynamicpropertiesofether-linkedphospholipidbilayermembraneshaveindicatedthatincontrasttoester-linkedphospholipid,theformationofthenon-bilayerstructuretakesplacespontaneously.Thisisattributedtotheweakerinteractionbetweenpolarheadgroupsintheether-linkedthanthatintheester-linkedphospholipids.Ithasalsoshownthatthephasebehavioroftheether-linkedphospholipidbilayermembranesinambientpressureisalmostequivalenttothatoftheester-linkedphospholipidbilayermembranesunderhightemperaturesandpressures,andthedifferenceinthephasebehaviordecreaseasthealkyl-chainlengthincreases.Duetodistinctivepropertiesofetherlipids,liposomesmadefrometherlipidsexhibitveryuniquecharacteristicsandperformance:a)theetherbondsaremorestablethanesterlinkagesoverawiderangeofacidicoralkalinepH;b)stABIlitypropertiesoftheliposomesisenhancedbybipolarlipids,andthesaturatedalkylchainsgivesstabilitytowardsdegradationinoxidativeconditions;c)theunusualstereochemistryoftheglycerolbackboneenhancetheresistanceagainsttheattacksbyotherorganismphospholipases.Lyophosome™productcatalogiscomposedofalargeselectionoffreeze-driedliposomeswithvarioustypesoflipidsandwiderangeofzetapotentialsanddifferentproperties. Lyophosome™productsshouldbeusedbyscientistswhounderstandliposomeformulationandhavetheproperequipmenttocheckthesize,separatenon-encapsulateddrugsanddotheproperassays.Freeze-driedliposomescannotbeusedblindly.PhospholipaseA2(PLA2)cannothydrolyzetheetherlipidliposomes.Dietherlipidsdonotgothroughhydrolysisduetohavinganetherbondinsteadofanacylbondandthereforetodothat,theyareasuitablecandidateforexperimentsthatneedstobeperformedatahighertemperatureforanextendedperiodoftime. Formoreinformationabouthydrolysisandoxidationofphospholipidssee here.ThestructureofDOPCcontainingdiesterbondandpronetohydrolysis.Thestructureof18:1dietherlipidwhichcannotbehydrolyzed.Saturateddietherlipidscanneitherbehydrolyzednoroxidized.Thestructureof18:0dietherlipidwhichcanneitherbehydrolyzednoroxidized.