Rabbit anti-Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody, Alexa Fluor 680/兔抗小鼠IgG (H+L)交叉吸附二抗,Alexa Fluor 680
货号:A-21065
规格:1 mg
价格:3191
产品类型:荧光二抗
品牌:Thermo Fisher
抗原:Gamma Immunoglobins Heavy and Light chains
物种:小鼠
宿主:兔
抗体亚型:IgG
荧光染料:Alexa Fluor 680
点击查看所有Alexa Fluor 荧光二抗
抗体类型: | 荧光二抗 | 同型对照: | |
浓度: | 2 mg/mL | 用法: | 1-10 μg/mL (ICC);1-10 μg/mL (IF); 0.04-0.2 μg/mL (WB) |
产品详细信息This secondary antibody is designed for fluorescent Western blot detection on various near-infrared fluorescence instruments. This antibody can be used for multi-color and multiplexing detection when using other antibodies conjugated to compatible Alexa Fluor™ dyes and wavelengths. Other applications of this antibody include immunofluorescent and fluorescent imaging applications when using instrumentation with appropriate excitation and detection capabilities. 靶标信息IgM (Immunoglobulin M) is expressed intracellularly during the early stages of B lymphopoiesis, and then on the surface of more mature B cells in the bone marrow and peripheral B cells. The isotype of a primary antibody and its application can result in background staining. Primary antibody background noise can be caused by binding to Fc receptors on target cells; by non-specific interactions with cellular proteins, carbohydrates, and lipids; or by cell autofluorescence. Isotype control antibodies can act as negative controls to help differentiate non-specific background signal from specific antibody signal because they have no relevant specificity to a target antigen. While isotype controls are most commonly used in flow cytometry, they are also useful in other applications such as chromatin immunoprecipitation (ChIP), immunohistochemistry, and gel shifts. Isotype controls should match with the primary antibody species and isotype so that the level of specific staining by the primary antibody may be accurately determined. If using directly labeled primary antibodies, the isotype control works best if conjugated with the same label as the test antibody.
数据 |
Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody (A-21065) in WBWestern blot analysis was performed on whole cell extracts (30 µg lysate) of U-87 MG (Lane 1) and HeLa (Lane 2). The blots were probed with Anti-SOD1 Mouse Monoclonal Antibody (Product # MA1-105, 2 µg/mL) and detected using Rabbit-anti Mouse IgG Cross Adsorbed Secondary Antibody Alexa Fluor-680 (Product # A-21065) at dilutions 0.04 µg/mL (Fig. 1), 0.1 µg/mL (Fig. 2) and 0.2 µg/mL (Fig. 3). A 18 kDa band corresponding to SOD1 was observed. Known quantity of protein samples were electrophoresed using Novex® NuPAGE®12 % Bis-Tris gel (Product # NP0342BOX), XCell SureLock™ Electrophoresis System (Product # EI0002) and Novex® Sharp Pre-Stained Protein Standard (Product # LC5800). Resolved proteins were then transferred onto a nitrocellulose membrane with iBlot® 2 Dry Blotting System (Product # IB21001). The membrane was probed with the relevant primary and secondary antibody after blocking with 5 % skimmed milk. Fluorescent detection was performed using the Odyssey® Fc imaging system (Li-cor Biosciences). |
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参考文献: |
1. Molecular medicine reportsTime-dependent homeostasis between glucose uptake and consumption in astrocytes exposed to CoCl₂ treatment.2. Journal of visualized experiments : JoVECycloheximide Chase Analysis of Protein Degradation in Saccharomyces cerevisiae. |
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