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- 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:
PerCP anti-mouse Ly-6G Antibody
- 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: | ¥1800.0 |
|---|---|---|---|
| 规格: | 100 µg | 产品价格: | ¥5100.0 |
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 under optimalconditions.
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 million cellsin 100 µl volume. It is recommended that the reagent be titrated for optimal performance for eachapplication.
* PerCP has a maximum absorption of 482 nm and a maximum emission of 675 nm.
Excitation Laser :Blue Laser (488 nm)
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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. Rudd JM, et al. 2019. Front Cell Infect Microbiol. 0.45. PubMed
2. Platt DJ, et al. 2021. Cell Reports. 35(6):109113. PubMed
3. Nagai Y, et al. 2019. Front Immunol. 10:174. PubMed
4. Zhang S, et al. 2019. Cell Metab. 29:443. PubMed
5. Sun L, et al. 2020. J Immunol. 2177:204. PubMed
6. Rohner L, et al. 2020. Sci Rep. 0.570833333. PubMed
7. Liu S, et al. 2020. Cell Host & Microbe. 26(6):779-794.e8.. PubMed
8. Trinh HKT, et al. 2019. J Cell Mol Med. 23:3441. PubMed
9. Akk A, et al. 2019. Mol Immunol. 114:629. PubMed
10. Robles-Oteiza C, et al. 2021. Dis Model Mech. 14:. PubMed
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