F(ab')2-Goat anti-Human IgG (H+L) Secondary Antibody, Qdot 655/F(ab')2-山羊抗人IgG (H+L)二抗,Qdot 655

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F(ab')2-Goat anti-Human IgG (H+L) Secondary Antibody, Qdot 655/F(ab')2-山羊抗人IgG (H+L)二抗,Qdot 655

货号:Q-11221MP

规格:200 µL

价格:6512

产品类型:荧光二抗

品牌:Thermo Fisher

抗原:Gamma Immunoglobins Heavy and Light chains

物种:人

宿主:山羊

抗体亚型:IgG

荧光染料:Qdot 655

类型:

二抗

同型对照:
浓度:

用法:

1:50(Flow);1:50(ICC);

1:50(I(IHC);1:50(WB)

产品详细信息Qdot nanocrystals are composed of semi-conductor material to generate a fluorescent particle which is exceptionally bright and does not photobleach. Qdot nanocrystals paired with the correct optical filters are as much as 50 times brighter than traditional organic dyes.靶标信息Anti-Human secondary antibodies are affinity-purified antibodies with well-characterized specificity for human 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, secondaryantibodies 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
Human IgG (H+L) Secondary Antibody (Q-11221MP) in IFA mouse intestinal section visualized using fluorescent Qdot® nanocrystal conjugates. Actin was labeled with a mouse anti-actin monoclonal antibody and visualized using red-fluorescent Qdot® 655 goat F (ab')2anti-mouse IgG (Product # Q11022MP,Product # Q-11221MP). Laminin was labeled with a rabbit anti-laminin polyclonal antibody and visualized using green-fluorescent Qdot® 525 goat F (ab')2anti-rabbit IgG (Product # Q-11441MP). Nuclei were stained with blue-fluorescent Hoechst 33342 (H1399, H3570, H21492). Image contributed by Thomas Deerinck and Mark Ellisman, The National Center for Microscopy and Imaging Research, San Diego, CA
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