Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 555/羊抗鼠 IgG (H+L) 高交叉吸附荧光二抗,Alexa Fluor Plus 555
货号:A32727
规格:1 mg
价格:3832
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:山羊
抗体亚型:IgG
荧光染料:Alexa Fluor plus 555
36个不同种属、不同荧光的Alexa Fluor plus荧光二抗点击表格中的货号,可跳转到相应的产品页。
| AF Plus Secondary Antibody products |
| AF Plus 488 | AF Plus 555 | AF Plus 594 | AF Plus 647 | AF Plus 680 | AF Plus 800 |
羊抗兔 | A32731 | A32732 | A32740 | A32733 | A32734 | A32735 |
羊抗鼠 | A32723 | A32727 | A32742 | A32728 | A32729 | A32730 |
羊抗鸡 | A32931 | A32932 | A32759 | A32933 | A32934 | A32935 |
驴抗羊 | A32814 | A32816 | A32758 | A32849 | A32860 | A32930 |
驴抗兔 | A32790 | A32794 | A32754 | A32795 | A32802 | A32808 |
驴抗鼠 | A32766 | A32773 | A32744 | A32787 | A32788 | A32789 |
产品优势:1. 更多荧光选择(从480到800),更多种属选择;2. 更好的光稳定性,更高信噪比,更高灵敏度,经过交叉吸附检测;3. 发布1年多已经有多达99篇高分文章引用;4. 适用于ICC/IF/WB等实验应用。
抗体类型: | 荧光二抗 | 同型对照: | |
浓度: | 2mg/mL | 用法: | 1-10µg/mL(ICC);1-10µg/mL(IF);0.1-0.4µg/mL(WB) |
产品详细信息To minimize cross-reactivity, the goat anti-mouse IgG whole antibodies have been pre cross-adsorbed against bovine IgG, goat IgG, rabbit IgG, rat IgG, human IgG, and human serum. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in less background staining and cross-reactivity. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. Further passages through additional columns result in highly cross-adsorbed preparations of secondary antibody. The benefits of these extra steps are apparent in multiplexing/multicolor-staining experiments where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins.Using conjugate solutions: Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment. This step will help eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining. Because staining protocols vary with application, the appropriate dilution of antibody should be determined empirically.靶标信息Obtain superior images with the new Invitrogen™ Alexa Fluor™ Plus secondary antibodies. Make your low abundant targets visible, minimize time spent optimizing, and make your precious samples count. Alexa Fluor™ Plus secondary antibodies provide brighter signal while having lower cross-reactivity compared to leading Alexa Fluor secondary antibodies, providing you with higher sensitivity and better signal-to-noise for your critical experiments.Alexa Fluor Plus secondary antibodies represent an advancement in fluorescent conjugate technology. Alexa Fluor Plus secondary antibodies are conjugated using new, proprietary dye chemistry and are pre-adsorbed to reduce background and cross-reactivity so you can generate stunning images. Alexa Fluor Plus secondary antibodies provide up to 4.2 fold higher signal-to-background in imaging applications and up to 5.8 fold higher signal-to-background in fluorescent western applications compared to Alexa Fluor secondary conjugates.For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization. |
数据 |
Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody (A32727) in IFImmunofluorescent analysis of glial fibrillary acidic protein (GFAP) in E18 Sparague Dawley primary cortical neuronal cells containing astrocytes. The cells were fixed with 4% formaldehyde for 15 mins, permeabilized with 0.25% Triton X-100 in PBS for 10 mins, and blocked with 3% BSA in PBS for 30 mins at RT. Cells were stained with a GFAP mouse monoclonal antibody (Product # MA5-12023) at a dilution of 1:200 in 3% BSA in PBS for 1 hr at RT, and then incubated with Invitrogen Alexa Fluor Plus 555 goat anti-mouse IgG secondary antibody (Product # A32727) at a dilution of 1:1000 for 1 hr at RT. Nuclei were stained with Hoechst 33342 (product # H3570). The image contains overlay of GFAP (orange) and nuclei (blue). Images were taken on a Zeiss LSM 710 confocal microscope at 40X magnification.Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody (A32727) in IFImmunofluorescent analysis of Cytochrome C in A549 cells. The cells were fixed with 4% formaldehyde for 15 mins, permeabilized with 0.25% Triton X-100 in PBS for 10 mins, and blocked with 3% BSA in PBS for 30 mins at RT. Cells were stained with a Cytochrome C mouse monoclonal antibody (Product # 33-8200) at a dilution of 1:200 in 3% BSA in PBS for 1 hr at RT, and then incubated with Invitrogen Alexa Fluor Plus 555 goat anti-mouse IgG secondary antibody (Product # A32727) at a dilution of 1:1000 for 1 hr at RT. Nuclei were stained with Hoechst 33342 (Product # H3570). The image contains overlay of Cytochrome C (orange) and nuclei (blue). Images were taken on a Zeiss LSM 710 confocal microscope at 40X magnification.Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody (A32727) in WBWestern blot analysis of Heat Shock Protein 60 (Hsp60) and Actin was performed by loading 3-fold serial dilutions of A431 whole cell lysate (starting at 15ug) and 2ul of the PageRuler Prestained NIR Protein Ladder (Product # 26635) per well onto a 4-20% Tris-HCl polyacrylamide gel. Proteins were transferred to Nitrocellulose Membranes (Product # 88018) and blocked with Fluorescence Blocker for 30 min. Membranes were probed with a Hsp60 monoclonal antibody (Product # MA3-012) at a dilution of 1:500 and a Actin monoclonal antibody at a dilution of 1:1000 (Product # MA1-744) overnight at 4°C on a rocking platform, washed with TBST, and probed with an Invitrogen Alexa Fluor Plus 555 Goat anti-Mouse IgG secondary antibody (Product # A32727) at dilutions of 1:10,000 for 45 minutes. Blots were imaged on a fluorescence imaging system. |
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二抗荧光二抗免疫组化一抗标签抗体 |
技术参数 产品优点 1.特异性强;2.亮度高,耐淬灭,对PH值不敏感;3.能高灵敏的检测低丰度蛋白。
产品应用 ICC;IF;WB
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