Goat anti-Rabbit IgG, Alexa Fluor 594,Goat anti-Rabbit IgG, Alexa Fluor 594/山羊抗兔IgG,Alexa Fluor 594

2024-10-23

Goat anti-Rabbit IgG, Alexa Fluor 594/山羊抗兔IgG,Alexa Fluor 594

货号:GRB2705,GRB2710

规格:50 μL,100 μL

价格:300,500

产品类型:荧光二抗

品牌:PBM

物种:兔

宿主:山羊

抗体亚型:IgG

荧光染料:Alexa Fluor 594

抗体类型:荧光二抗同型对照:IgG
浓度 2 mg/mL用法:2 µg/mL(ICC/IF);1-10 µg/mL(Flow)
产品详细信息

To minimize cross-reactivity, these goat anti-rabbit IgG whole antibodies have been cross-adsorbed against human IgG, human serum, mouse IgG, mouse serum, and bovine serum. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in higher sensitivity and less background staining. 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. The benefits of this extra step are apparent in multiplexing/multicolor-staining experiments (e.g., flow cytometry) where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there are may be the presence of endogenous immunoglobulins.Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 594 dye is a bright, red-fluorescent dye with excitation ideally suited to the 594 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 594 dye is pH-insensitive over a wide molar range. Probes with high fluorescence quantum yield and high photostability allow detection of low-abundance biological structures with great sensitivity. Alexa Fluor 594 dye molecules can be attached to proteins at high molar ratios without significant self-quenching, enabling brighter conjugates and more sensitive detection. The degree of labeling for each conjugate is typically 2-8 fluorophore molecules per IgG molecule; the exact degree of labeling is indicated on the certificate of analysis for each product lot.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. For the fluorophore-labeled antibodies a final concentration of 1-10 µg/mL should be satisfactory for most immunohistochemistry and flow cytometry applications.Product will be shipped at Room Temperature.

靶标信息

Anti-Rabbit secondary antibodies are affinity-purified antibodies with well-characterized specificity for rabbit immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.

数据

The peripheral nervous system of a wild-type (Canton-S) Drosophila melanogaster embryo labeled with the monoclonal 22c10 antibody (which detects a microtubule-associated protein) and subsequently visualized using green-fluorescent Alexa Fluor® 488 Rabbit Anti-Mouse IgG antibody (Product # A-11059). The actively dividing cells of the developing denticle bands were labeled with a rabbit anti-histone-H3 antibody and visualized using red-fluorescent Alexa Fluor® 594 Goat Anti-Rabbit IgG antibody (Product # A-11012). Finally, the nuclei, which are concentrated in the central nervous system, were counterstained with blue-fluorescent DAPI (Product # D1306, D3571, D21490). Image contributed by Neville Cobbe, University of Edinburgh.

Inhibition of NSC proliferation and DNA damage induced by the conditioned medium of BeWo cells overexpressing CYP11A1 and intervention by vitamin D3. (A) KI-67 immunostaining in NSCs. (B) CCK-8 proliferation assay. (C, D) γH2AX immunostaining in NSCs. CYP, BeWo cells overexpressing CYP11A1. Vehicle, BeWo cells transfected with vehicle. CTL, control. CYP_VD_L, BeWo cells overexpressing CYP11A1 and treated with a low-dose of vitamin D3 (2 µM). CYP_VD_H, BeWo cells overexpressing CYP11A1 and treated with a high-dose of vitamin D3 (5 µM). Statistical analysis was performed on the means from three independent experiments using one-way analysis of variance (ANOVA) with Tukey’s post hoc test. ***P < 0.001. Scale bars, 20 µm. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33659272), licensed under a CC BY license.

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