货号 | IC108P |
别名 | immunoglobulin heavy constant gamma 1 (G1m marker) | 全称 | Immunoglobulin G |
应用 | Control() |
目标/特异性 | Serum was obtained from naive (non-immunized) goats. |
使用方法 | Control: Negative control for use in conjunction with R&D Systems antibodies for flow cytometry applications. This isotype control has been derivatized with a quantity of fluorochrome that matched the F/P (fluorochrome/protein) ratio of R&D Systems specific polyclonal antibodies. The recommended concentration is 10 μL/106cells.
This reagent has not been tested for immunohistochemistry. |
来源 | Polyclonal Goat IgG |
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. Prerequisites for Functional Interleukin 31 Signaling and Its Feedback Regulation by Suppressor of Cytokine Signaling 3 (SOCS3). | |
纯化方式 | Protein A or G purified |
免疫原 | NA |
标记 | Phycoerythrin |
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 Goat IgGControl by Flow Cytometry bEnd.3 mouse endothelioma cell line was stained with GoatAnti-Mouse VEGF R3/Flt-4 PE-conjugated Antigen Affinity-purifiedPolyclonal Antibody (Catalog #FAB743P,filled histogram) or Goat IgG PE-conjugated Isotype Control Antibody(Catalog # IC108P, open histogram). View our protocol for StainingMembrane-associated Proteins. |