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品牌： BD Pharmingen
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对比
咨询反应种属：
Mouse (QC Testing)
Mouse (QC Testing)
来源宿主：
Armenian Hamster IgG1, λ2
Armenian Hamster IgG1, λ2
产品介绍
产品信息
耦联标记
PerCP-Cy5.5
抗原名称
CD11c (Integrin aX)
宿主
Armenian Hamster IgG1, λ2
免疫原
C57BL/6 Mouse Intestinal Intraepithelial Lymphocytes
简单描述
The HL3 monoclonal antibody specifically binds to the integrin αx chain of gp150, 95 (CD11c/CD18). CD11c is expressed on dendritic cells, CD4- CD8+ intestinal intraepithelial lymphocytes (IEL) and some NK cells. It is upregulated on IEL and lymph-node T cells following
in vivo
activation. Cells of the monocyte/macrophage lineage have been reported to express low levels of CD11c. CD11c plays a role in binding of iC3b.
商品描述
HL3
The HL3 monoclonal antibody specifically binds to the integrin αx chain of gp150, 95 (CD11c/CD18). CD11c is expressed on dendritic cells, CD4- CD8+ intestinal intraepithelial lymphocytes (IEL) and some NK cells. It is upregulated on IEL and lymph-node T cells following
in vivo
activation. Cells of the monocyte/macrophage lineage have been reported to express low levels of CD11c. CD11c plays a role in binding of iC3b.
同种型
Armenian Hamster IgG1, λ2
克隆号
克隆 HL3 (RUO)
浓度
0.2 mg/ml
产品详情
PerCP-Cy5.5
PerCP-Cy5.5 dye is part of the BD blue family of dyes. This tandem fluorochrome is comprised of a fluorescent protein complex (PerCP) with an excitation maximum (Ex Max) of 482 nm and an acceptor dye with an emission maximum (Em Max) at 676 nm. PerCP-Cy5 is designed to be excited by the blue laser (488-nm) and detected using an optical filter centered near 680 nm (e.g., a 695/40 nm bandpass filter). The donor dye can be partially excited by the Violet (405-nm) laser resulting in cross-laser excitation and fluorescence spillover. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
PerCP-Cy5.5
Blue 488 nm
482 nm
676 nm
应用
实验应用
Flow cytometry (Routinely Tested)
反应种属
Mouse (QC Testing)
目标/特异性
CD11c (Integrin αX)
背景
别名
Cd11c; Itgax; Integrin alpha-X; Integrin αX; Cr4; Complement receptor 4
制备和贮存
存储溶液
Aqueous buffered solution containing protein stabilizer and ≤0.09% sodium azide.
保存方式
Aqueous buffered solution containing protein stabilizer and ≤0.09% sodium azide.
文献
文献
研发参考(10)
1. Barclay NA, Brown MH, Birkeland ML, et al, ed. The Leukocyte Antigen FactsBook. San Diego, CA: Academic Press; 1997.
2. Burt BM, Plitas G, Stableford JA, et al. CD11c identifies a subset of murine liver natural killer cells that responds to adenoviral hepatitis. J Leukoc Biol. 2008; 84(4):1039-1046. (Biology).
3. Fagarasan S, Muramatsu M, Suzuki K, Nagaoka H, Hiai H, Honjo T. Critical roles of activation-induced cytidine deaminase in the homeostasis of gut flora. Science. 2002; 298(5597):1424-1427. (Biology).
4. Gao JX, Liu X, Wen J, et al. Differentiation of monocytic cell clones into CD8 alpha+ dendritic cells (DC) suggests that monocytes can be direct precursors for both CD8 alpha+ and CD8 alpha- DC in the mouse. J Immunol. 2003; 170(12):5927-5935. (Biology).
5. Huleatt JW, Lefrançois L. Antigen-driven induction of CD11c on intestinal intraepithelial lymphocytes and CD8+ T cells in vivo.. J Immunol. 1995; 154(11):5684-93. (Immunogen: Immunoprecipitation).
6. Larson RS, Springer TA. Structure and function of leukocyte integrins. Immunol Rev. 1990; 114:181-217. (Biology).
7. Maraskovsky E, Brasel K, Teepe M, et al. Dramatic increase in the numbers of functionally mature dendritic cells in Flt3 ligand-treated mice: multiple dendritic cell subpopulations identified. J Exp Med. 1996; 184(5):1953-1962. (Biology).
8. Metlay JP, Witmer-Pack MD, Agger R, Crowley MT, Lawless D, Steinman RM. The distinct leukocyte integrins of mouse spleen dendritic cells as identified with new hamster monoclonal antibodies. J Exp Med. 1990; 171(5):1753-1771. (Biology).
9. Pulendran B, Lingappa J, Kennedy MK, et al. Developmental pathways of dendritic cells in vivo: distinct function, phenotype, and localization of dendritic cell subsets in FLT3 ligand-treated mice. J Immunol. 1997; 159(5):2222-2231. (Biology).
10. Zola H. Leukocyte and stromal cell molecules : the CD markers. Hoboken, N.J.: Wiley-Liss; 2007.
参考图片
Flow cytometric analysis of CD11c on mouse dendritic cells. C57BL/6 splenocytes treated with 5 ng/mL GM-CSF were stained either with a PerCP-Cy™5.5 Hamster IgG1, λ1 isotype control (Cat. No. 560554; shaded histogram) or with the PerCP-Cy™5.5 Hamster Anti-Mouse CD11c antibody (Cat. No. 560584; unshaded histogram). Histograms were derived from gated events based on light scattering characteristics for dendritic cells. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD11c on mouse dendritic cells. C57BL/6 splenocytes treated with 5 ng/mL GM-CSF were stained either with a PerCP-Cy™5.5 Hamster IgG1, λ1 isotype control (Cat. No. 560554; shaded histogram) or with the PerCP-Cy™5.5 Hamster Anti-Mouse CD11c antibody (Cat. No. 560584; unshaded histogram). Histograms were derived from gated events based on light scattering characteristics for dendritic cells. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
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