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BD Pharmingen- PE Mouse Anti-Human CD89_BD Pharmingen

产品信息
荧光素标记
PE
抗原名称
CD89
宿主
Mouse BALB/c IgG1, κ
免疫原
Purified Human FcαR
简单描述
The A59 monoclonal antibody specifically recognizes CD89. CD89 is the Fc receptor for IgA (FcαR), a 55-75 kDa glycoprotein expressed exclusively on cells of granulocytic and monocyte/macrophage lineages in peripheral blood, but not on lymphocytes. It is also expressed on promyelocytes in bone marrow and in the cytoplasm of fixed monocytes. This mAb does not block IgA binding and is more efficient than native IgA ligands in the isolation of FcαR molecules. FcαR plays a role in triggering phagocytosis and respiratory burst.
商品描述
A59 The A59 monoclonal antibody specifically recognizes CD89. CD89 is the Fc receptor for IgA (FcαR), a 55-75 kDa glycoprotein expressed exclusively on cells of granulocytic and monocyte/macrophage lineages in peripheral blood, but not on lymphocytes. It is also expressed on promyelocytes in bone marrow and in the cytoplasm of fixed monocytes. This mAb does not block IgA binding and is more efficient than native IgA ligands in the isolation of FcαR molecules. FcαR plays a role in triggering phagocytosis and respiratory burst.
同种型
Mouse BALB/c IgG1, κ
克隆号
克隆 A59 (RUO)
产品详情
PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
应用
实验应用
Flow cytometry (Routinely Tested)
推荐用量
20 µl
反应种属
Human (QC Testing)
目标/特异性
CD89
背景
别名
FCAR; IgA Fc receptor; FcαR; FcalphaRI; CTB-61M7.2
制备和贮存
存储溶液
Aqueous buffered solution containing BSA and ≤0.09% sodium azide.
保存方式
Aqueous buffered solution containing BSA and ≤0.09% sodium azide.
文献
文献
研发参考(4) 1. Monteiro RC, Cooper MD, Kubagawa H. Molecular heterogeneity of Fc alpha receptors detected by receptor-specific monoclonal antibodies. J Immunol. 1992; 148(6):1764-1770. (Biology). 2. Schlossman SF. Stuart F. Schlossman .. et al., ed. Leucocyte typing V : white cell differentiation antigens : proceedings of the fifth international workshop and conference held in Boston, USA, 3-7 November, 1993. Oxford: Oxford University Press; 1995. 3. Shen L, Collins JE, Schoenborn MA, Maliszewski CR. Lipopolysaccharide and cytokine augmentation of human monocyte IgA receptor expression and function. J Immunol. 1994; 152(8):4080-4086. (Biology). 4. Shen L. A monoclonal antibody specific for immunoglobulin A receptor triggers polymorphonuclear neutrophil superoxide release. J Leukoc Biol. 1992; 51(4):373-378. (Biology).
数据库链接
Entrez-Gene ID
2204

参考图片

Flow cytometric analysis of CD89 expression on human peripheral blood granulocytes. Whole blood was stained with either PE Mouse Anti-Human CD89 (Cat. No. 555686; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristics of viable granuloctyes. Flow cytometry was performed on a BD FACScan™ system.

Flow cytometric analysis of CD89 expression on human peripheral blood granulocytes. Whole blood was stained with either PE Mouse Anti-Human CD89 (Cat. No. 555686; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristics of viable granuloctyes. Flow cytometry was performed on a BD FACScan™ system.

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