| 货号 | IC0041G |
| 别名 | IgG2B | 全称 | Immunoglobulin G2B Fc |
| 反应种属 | Mouse |
| 应用 | Control() |
| 目标/特异性 | Selected for use as mouse IgG2B isotype control for flow cytometry applications. |
| 使用方法 | Control: Negative control for use in conjunction with R&D Systems antibodies. This isotype control has been derivatized with a quantity of fluorochrome that matched the F/P(fluorochrome/protein) ratio of R&D Systems monoclonal reagents. The recommended concentration is 5 μL/106cells. |
| 来源 | Monoclonal Mouse IgG2B Clone # 133303 |
| 产品组分 |
| 供应商 | R&D Systems |
| 应用文献 | |
| R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions. Base-modified UDP-sugars reduce cell surface levels of P-selectin glycoprotein 1 (PSGL-1) on IL-1?-stimulated human monocytes | |
| 纯化方式 | Protein A or G purified from hybridoma culture supernatant |
| 免疫原 | KLH |
| 标记 | Alexa Fluor 488 |
| 背景 | R&D Systems offers a range of secondary antibodies and controls for flow cytometry, immunohistochemistry, and Western blotting. We provide species-specific secondary antibodies that are available with a variety of conjugated labels. Our NorthernLights fluorescent secondary antibodies are bright and resistant to photobleaching. We are currently offering secondary antibodies recognizing mouse, rat, goat, sheep, and rabbit IgG as well as chicken IgY. These reagents are available with three distinct excitation and emission maxima, making them ideal for multi-color fluorescence microscopy. |
| 运输条件 | Blue Ice |
| 存放说明 | 4℃ |
| 参考文献 |
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Detection of Mouse IgGControl by Flow Cytometry Human peripheral blood mononuclear cell (PBMCs) were stainedwith Mouse Anti-Human Plexin A1 Alexa Fluor® 488‑conjugatedMonoclonal Antibody (Catalog # FAB65361G,filled histogram) or Mouse IgG Alexa Fluor® 488-conjugated IsotypeControl Antibody (Catalog # IC0041G, open histogram). View our protocol for StainingMembrane-associated Proteins. |
