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Goat anti-Chicken IgY (H+L) Secondary Antibody, Alexa Fluor™ 568

类型:荧光二抗
品牌:Thermo Fisher
种属:Chicken
应用:Flow,WB,IHC,ICC/IF
抗体亚型:IgG
偶联物:Alexa Fluor 568/AF568
宿主:Goat
浓度:2 mg/mL

规格: 1mg

货号: A11041

价格: ¥3359.00

优惠: ¥2351.00

数量:

应用

建议稀释比

免疫细胞化学 (ICC/IF)

1-10 µg/mL

流式细胞分析 (Flow)

1-10 µg/mL

免疫组化 (IHC)

1-10 µg/mL

免疫印迹 (WB)

1:5,000-1:10,000

 

产品详细信息

 

Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 568 dye is a bright, orange/red-fluorescent dye with excitation ideally suited to the 568 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 568 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 568 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-Chicken secondary antibodies are affinity-purified antibodies with well-characterized specificity for the chicken 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.

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