相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 供应商:
齐源
- 库存:
999
- 靶点:
Ly-6G
- 级别:
Ly-6G Antibody
- 目录编号:
Ly-6G Antibody
- 克隆性:
单克隆
- 抗原来源:
大鼠
- 保质期:
Ly-6G Antibody
- 抗体英文名:
Cyanine5.5 anti-mouse Ly-6G Antibody-PerCP
- 抗体名:
Ly-6G Antibody
- 标记物:
Ly-6G Antibody
- 宿主:
大鼠
- 适应物种:
小鼠
- 免疫原:
Ly-6G Antibody
- 亚型:
Ly-6G Antibody
- 形态:
Ly-6G Antibody
- 应用范围:
FC
- 保存条件:
2-8℃
- 浓度:
0.2 mg/ml
- 规格:
25 µg/100 µg
| 规格: | 25 µg | 产品价格: | ¥1900.0 |
|---|---|---|---|
| 规格: | 100 µg | 产品价格: | ¥5900.0 |
Description :Lymphocyte antigen 6 complex, locus G (Ly-6G), a 21-25 kD GPI-anchored protein, isexpressed on the majority of myeloid cells in bone marrow and peripheral granulocytes.
Verified Reactivity :Mouse
Antibody Type :Monoclonal
Host Species :Rat
Immunogen :Ly-6G transfected EL-4J cell line.
Formulation :Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation :The antibody was purified by affinity chromatography, and conjugated with PerCP/Cyanine5.5under optimal conditions.
Concentration :0.2 mg/ml
Storage & Handling :The antibody solution should be stored undiluted between 2°C and 8°C, and protected fromprolonged exposure to light. Do not freeze.
Application :FC - Quality tested
Recommended Usage :Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometricanalysis. For flow cytometric staining, the suggested use of this reagent is ≤ 0.25 µg per 10 cellsin 100 µl volume. It is recommended that the reagent be titrated for optimal performance for eachapplication.
* PerCP/Cyanine5.5 has a maximum absorption of 482 nm and a maximum emission of 690 nm.
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验1. Fleming TJ, et al. 1993. J. Immunol. 151:2399. (FC)
2. Daley JM, et al. 2008. J. Leukocyte Biol. 83:1. (FC)
3. Dietlin TA, et al. 2007. J. Leukocyte Biol. 81:1205. (FC)
4. Daley J, et al. 2007. J. Leukocyte Biol. doi:10.1189. (Deplete) PubMed
5. Tadagavadi RK, et al. 2010. J. Immunol. 185:4904. PubMed
6. Sumagin R, et al. 2010. J. Immunol. 185:7057. PubMed
7. Guiducci C, et al. 2010. J. Exp Med. 207:2931. PubMed
8. Fujita M, et al. 2011. Cancer Res. 71:2664. PubMed
9. Van Leeuwen, et al. 2008. Arterioscler. Thromb. Vasc. Biol. 28:84. (IHC)
10. Kowanetz M, et al. 2010. P. Natl. Acad. Sci. USA 107:21248. [supplementary data] (IHC)
11. Esbona K, et al. 2016. Breast Cancer Res. 18:35. (IHC)
12. Wojtasiak M, et al. 2010. J. Gen. Virol. 91:2158. (FC, Deplete)
13. Jaeger BN, et al. 2012. J. Exp. Med. 209:565. (Deplete)
14. Wozniak KL, et al. 2012. BMC Immunol. 13:65 (FC, Deplete)
15. Ribechini E, et al. 2009. Eur. J. Immunol. 39:3538.
16. Ng LG, et al. 2011. J Invest. Dermatol. 131:2058. PubMed
17. Ma C, et al. 2012. J. Leukoc. Biol. 92:1199.
18. McCartney-Francis, N, et al. 2014. J Leukoc. Biol. 96:917. PubMed
19. Her Z, et al. 2014. EMBO Mol. Med. 7:24. PubMed
20. Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
21. Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed
Product Citations:
1. Cho SM et al. 2018. Journal of neurochemistry. 148(5):625-638 . PubMed
2. Delvecchio FR, et al. 2021. Cell Mol Gastroenterol Hepatol. 12:1543. PubMed
3. Ercoli G, et al. 2021. Front Immunol. 11:611661. PubMed
4. Wong Fok Lung T, et al. 2020. Nat Microbiol. 141:5. PubMed
5. Gern BH, et al. 2021. Cell Host Microbe. 29(4):594-606.e6. PubMed
6. Maschmeyer P, et al. 2017. J Autoimmun.. 10.1016/j.jaut.2017.11.005. PubMed
7. Misumi I et al. 2019. Cell Rep. 27(5):1387-1396 . PubMed
8. Merz SF, et al. 2019. Nat Commun. 10:2312. PubMed
9. Rodriguez-García A, et al. 2021. Nat Commun. 12:877. PubMed
10. Pan Y, et al. 2021. Front Cell Neurosci. 15:664312. PubMed
11. Su N, Xiong Y 2016. Sci Rep. 6:22658. PubMed
12. Kwon O, et al. 2016. Stem Cell Res. 16: 682-691. PubMed
大部分老师做流式实验时,会用到空白对照、单阳对照、同型对照、生物学对照等,用到 FMO 对照的比较少。尽管如此,FMO 对照在设置圈门时仍具有重要的参考价值。 一方面,FMO 对照有助于精确地设置阴阳性群体界限。我们在做多色实验时,可能会出现某些通道信号难以区分的情况,主要是因为其他某个荧光对该通道的干扰很大。FMO 对照(Fluorescence Minus One,荧光扣除一)减少了其中一个通道的荧光抗体,能够帮助衡量其它通道的荧光漏溢情况。 如下图所示,PerCP/Cyanine
流式抗体的选择和配色原则由于在流式细胞实验过程中,荧光抗体对单细胞悬液的标记效果直接影响实验的数据质量。因此,需要考虑各种影响流式抗体品质及检测效果的因素,例如抗体特异性、荧光素信号强弱、荧光素标记方式、同型对照等。本文介绍如何选择合适的流式抗体: 1、需要满足抗体选择的最基本条件:目标蛋白特异性,反应种属以及应用实验等。 靶标特异性:确定标记物名称,确定是细胞表面表达,还是细胞内表达。细胞内表达需要进行透膜。 物种来源:确定待测样本的种属来源。例如,抗小鼠的抗体,不能用于人的样本的检测
出现IgG 分子50 and 25 kDa 的重链和轻链条带。 5 二抗的选择 二抗应选用与使用的一抗相同的物种来源,例如:如果你的一抗是小鼠的单克隆抗体,二抗则选抗小鼠的二抗anti-mouse secondary。建议检查二抗说明书确保该抗体适用于你的检测应用, 二抗一般连接荧光素FITC 或发光团。 6 双重染色抗体的选择用未偶联一抗进行细胞培养物或组织切片的双重免疫染色要求一抗来源于不同物种并且二抗分别识别其中之一,二抗说明书应描述其与其它物种来源的免疫球蛋有否有交叉吸附。 想了解










