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BD Pharmingen- PE Mouse Anti-Human CD49b_BD Pharmingen

产品信息
荧光素标记
PE
抗原名称
CD49b (Integrin α2)
宿主
Mouse BALB/c IgG2a, κ
免疫原
Human PBMC and Platelets
简单描述
The 12F1 monoclonal antibody specifically binds to CD49b. CD49b is also known as the integrin α2 chain (VLA-α2), a member of the integrin family of extracellular matrix and cell-cell adhesion receptors. VLA-α2 is non-covalently associated with VLA-β1 chain (CD29) in the VLA-2 complex. α2 is expressed on numerous cell types including activated T cells, platelets, and long-term cultivated T cells. α2β1 is a well-established receptor for collagen. This antibody is useful for studies of integrin expression and function.
商品描述
12F1 The 12F1 monoclonal antibody specifically binds to CD49b. CD49b is also known as the integrin α2 chain (VLA-α2), a member of the integrin family of extracellular matrix and cell-cell adhesion receptors. VLA-α2 is non-covalently associated with VLA-β1 chain (CD29) in the VLA-2 complex. α2 is expressed on numerous cell types including activated T cells, platelets, and long-term cultivated T cells. α2β1 is a well-established receptor for collagen. This antibody is useful for studies of integrin expression and function.
同种型
Mouse BALB/c IgG2a, κ
克隆号
克隆 12F1 (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
CD49b (Integrin α2)
背景
别名
Integrin α2 chain; ITGA2; VLA-2 alpha; Platelet GPIa; Collagen receptor; BR
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. Hemler ME, Kawaguchi S, Bodorova J. CD49b cluster repoty. In: 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; 1995:1615-1616. 2. Hemler ME. VLA proteins in the integrin family: structures, functions, and their role on leukocytes. Annu Rev Immunol. 1990; 8:365-400. (Biology). 3. Knapp W. W. Knapp .. et al., ed. Leucocyte typing IV : white cell differentiation antigens. Oxford New York: Oxford University Press; 1989:1-1182. 4. 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.
数据库链接
Entrez-Gene ID
3673

参考图片

Flow cytometric profile of CD49B expression on human peripheral blood platelets. Platelets were stained with either PE Mouse Anti-Human CD49b (Cat. No. 555669, solid line histogram) or PE Mouse IgG2a, κ Isotype Control (Cat. No. 555574, dashed line histogram). Fluorescence histograms depicting CD49B expression (or Ig isotype control staining) was derived from gated events with the side and forward light-scatter characteristics of viable lymphocytes. Flow cytometry was carried on a BD FACSan™ System.

Flow cytometric profile of CD49B expression on human peripheral blood platelets. Platelets were stained with either PE Mouse Anti-Human CD49b (Cat. No. 555669, solid line histogram) or PE Mouse IgG2a, κ Isotype Control (Cat. No. 555574, dashed line histogram). Fluorescence histograms depicting CD49B expression (or Ig isotype control staining) was derived from gated events with the side and forward light-scatter characteristics of viable lymphocytes. Flow cytometry was carried on a BD FACSan™ System.

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