PE/Dazzle(TM) 594 anti-human CD31 303130 from BioLegend | Biocompare.com

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PE/Dazzle(TM) 594 anti-human CD31

BioLegend's PE/Dazzle(TM) 594 anti-human CD31 is a Mouse monoclonal antibody. The PE/Dazzle(TM) 594 anti-human CD31 Antibody was generated using PECAM1 as the antigen. It reacts with Homo Sapiens, Human, and Non-Human Primate. This antibody has been shown to work in applications such as: Flow Cytometry.

Description

PE/Dazzle(TM) 594 anti-human CD31 [WM59]

Product Specs
ItemPE/Dazzle(TM) 594 anti-human CD31
CompanyBioLegend
Price Pricing Info Supplier Page View Company Product Page
Catalog Number303130
Quantity100 tests
ApplicationsFlow Cytometry (FC)
Conjugate/TagPE_DZL594
FormatPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA)
ReactivityHuman, Cynomolgus, Rhesus
IsotypeIgG1, Kappa
CloneWM59
HostMouse
Antibody TypePrimary
NCBI Full Gene Nameplatelet and endothelial cell adhesion molecule 1
NCBI Gene AliasesCD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM
ClonalityMonoclonal
TargetCD31

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BioLegend

BioLegend

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Fax: 1-877-455-9587

Company Profile

Website: biolegend.com

(1) Morphological and phenotypic analyses of the human placenta using whole mount immunofluorescenceBiology of reproductionMay 1, 2014Meghan E Bushway, Scott A Gerber, Bruce M Fenton, Richard K Miller, Edith M Lord, Shawn P Murphy

(2) Regulation of human lung alveolar multipotent cells by a novel p38α MAPK/miR-17-92 axisThe EMBO journalAugust 15, 2012Oeztuerk-Winder F, Guinot A, Ochalek A, Ventura JJ.

(3) Targeting tumor-associated endothelial cells: anti-VEGFR2 immunoliposomes mediate tumor vessel disruption and inhibit tumor growthClinical cancer research : an official journal of the American Association for Cancer ResearchJanuary 15, 2012Wicki A, Rochlitz C, Orleth A, Ritschard R, Albrecht I, Herrmann R, Christofori G, Mamot C.

(4) Identification of functional endothelial progenitor cells suitable for the treatment of ischemic tissue using human umbilical cord bloodBloodJuly 1, 2007Nagano M, Yamashita T, Hamada H, Ohneda K, Kimura K, Nakagawa T, Shibuya M, Yoshikawa H, Ohneda O.

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