簡要描述:Invitrogen A-21202Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ 488產(chǎn)品信息應用建議稀釋比免疫組化 (IHC)
詳細介紹
品牌 | Thermofisher Scientific/賽默飛世爾 | 貨號 | A-21202 |
---|---|---|---|
規(guī)格 | 盒 | 供貨周期 | 一周 |
主要用途 | 科研單位實驗用 | 應用領域 | 醫(yī)療衛(wèi)生,食品,化工,生物產(chǎn)業(yè),制藥 |
Invitrogen A-21202
Invitrogen A-21202
Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ 488
產(chǎn)品信息
應用
建議稀釋比
免疫組化 (IHC)
1-10 µg/mL
免疫細胞化學 (ICC/IF)
0.2 µg/mL
產(chǎn)品規(guī)格
種屬反應
Mouse
宿主/亞型
Donkey / IgG
分類
Polyclonal
類型
Secondary Antibody
抗原
Gamma Immunoglobins Heavy and Light chains
偶聯(lián)物
Alexa Fluor™ 488查看其它偶聯(lián)染料
激發(fā)/發(fā)射光譜
499/520 nm查看光譜spectra
形式
Liquid
濃度
2 mg/mL
純化類型
purified
保存液
PBS, pH 7.5
內含物
5mM sodium azide
保存條件
4° C, store in dark
運輸條件
Ambient
RRID
AB_141607
靶標
IgG
交叉吸附
Against bovine, chicken, goat, guinea pig, hamster, horse, human, rabbit, rat, and sheep serum
抗體形式
Whole Antibody
產(chǎn)品詳細信息
To minimize cross-reactivity, these donkey anti-mouse IgG whole antibodies have been affinity-purified and show minimum cross-reactivity to bovine, chicken, goat, guinea pig, hamster, horse, human, mouse, rat, and sheep serum proteins. 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 may be the presence of endogenous immunoglobulins.
Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 488 dye is a bright, green-fluorescent dye with excitation ideally suited to the 488 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 488 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 488 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.
靶標信息
Anti-Mouse secondary antibodies are affinity-purified antibodies with well-characterized specificity for mouse 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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