
- SpeciesReactivityMouse
- SpecificityDetectsmouseCCL3/MIP‑1alphainWesternblots.InWesternblots, approximately25%cross-reactivitywithrecombinantmouseCCL4/MIP‑1beta isobserved andnocross-reactivitywithrecombinanthumanCCL1,2,3,5,7,8,11,13,14,15,16,17,18,21,22,23,24,25,28,recombinantmouseCCL1,2,6,7,9/10/MIP-1gamma,11,12,19,21,22,25,28,recombinantratCCL2orCCL20isobserved.NeutralizestheBIOLOGicalactivityofrecombinantmouseCCL3and willnotblockthebiologicalactivityofrecombinanthumanCCL3.
- SourceMonoclonalRatIgG2AClone#39624
- PurificationProteinAorGpurifiedfromhybridomaculturesupernatant
- ImmunogenE.coli-derivedrecombinantmouseCCL3/MIP-1alpha
Ala24-Ala92
Accession#P10855 - FormulationSuppliedinasalinesolutioncontainingBSAandSodiumAzide.
- LabelAlexaFluor488
- IntracellularStainingbyFlowCytometry5µL/106cellsSeebelow
- ShippingTheproductisshippedwithpolarpacks.Uponreceipt,storeitimmediatelyatthetemperaturerecommendedbelow.
- StABIlity&StorageProtectfromlight.Donotfreeze.
- 12monthsfromdateofreceipt,2to8°Cassupplied.
- Menten,P.etal.(2002)CytokineGrowthFactorRev.13:455.
- EntrezGeneIDs:6348(Human);20302(Mouse);25542(Rat);448787(Canine)
- AlternateNames:C-Cmotifchemokine3;MIP1-(a);AI323804;CCL3;chemokine(C-Cmotif)ligand3;G0S19-1;LD78a;LD78alpha;MIP1alpha;MIP-1alpha;Mip1a;MIP-1alpha;MIP1-alpha;Scya3
Background:
Themacrophageinflammatoryproteins1alphaand1beta,twocloselyrelatedbutdistinctproteins,wereoriginallyco-purifiedfrommediumconditionedbyaLPS-stimulatedmurinemacrophagecellline.MaturemouseCCL3/MIP-1alphasharesapproximately77%and70%aminoacididentitywithhumanCCL3/MIP-1alphaandmouseCCL4/MIP-1beta,respectively.MIP‑1proteinsareexpressedprimarilyinTcells,Bcells,andmonocytesafterantigenormitogenstimulation.TheMIP‑1proteinsaremembersofthebeta (C‑C)subfamilyofchemokines.
BothCCL3andCCL4aremonocytechemoattractantsinvitro.Additionally,theMIP‑1proteinshavebeenreportedtohavechemoattractantandadhesiveeffectsonlymphocytes,withCCL3andCCL4preferentiallyattractingCD8+andCD4+Tcells,respectively.CCL3hasalsobeenshowntoattractBcellsaswellaseosinophils.MIP‑1proteinshavebeenreportedtohavemultipleeffectsonhematopoieticprecursorcells,andCCL3hasbeenidentifiedasastemcellinhibitoryfactorthatcaninhibittheproliferationofhematopoieticstemcellsinvitroaswellasinvivo.Inthesameassays,CCL4wasreportedtobemuchlessactive.ThefunctionalreceptorforCCL3hasbeenidentifiedasCCR1andCCR5.
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