Rat anti-Mouse IgG2a Secondary Antibody, Super Bright 780, eBioscience/大鼠抗小鼠IgG2a二抗,Super Bright 780

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Rat anti-Mouse IgG2a Secondary Antibody, Super Bright 780, eBioscience/大鼠抗小鼠IgG2a二抗,Super Bright 780

货号:78-4210-82,78-4210-80

规格:100 µg,25 µg

价格:2995,0

产品类型:荧光二抗

品牌:eBioscience

物种:小鼠

宿主:大鼠

抗体亚型:其它

克隆号:m2a-15F8

荧光染料:Super Bright 780

类型:二抗同型对照:
浓度: 0.2 mg/mL 用法: 1.0 µg/test(Flow)
产品详细信息Description: The monoclonal antibody m2a-15F8 recognizes Mouse IgG2a antibodies and can be used as a second step reagent in flow cytometry and microscopy. The monoclonal does not recognize other mouse isotypes nor does it crossreact to rat IgG2a or any rat isotype antibodies.Applications Reported: This m2a-15F8 antibody has been reported for use in flow cytometric analysis.Applications Tested: This m2a-15F8 antibody has been tested by flow cytometric analysis of normal human peripheral blood cells. This may be used at less than or equal to 1.0 µg per test. A test is defined as the amount (µg) of antibody that will stain a cell sample in a final volume of 100 µL. Cell number should be determined empirically but can range from 10^5 to 10^8 cells/test. It is recommended that the antibody be carefully titrated for optimal performance in the assay of interest.Super Bright 780 is a tandem dye that can be excited with the violet laser line (405 nm) and emits at 780 nm. We recommend using a 780/60 bandpass filter. Please make sure that your instrument is capable of detecting this fluorochrome.In some experiments, we have observed that compensation values for Super Bright 780-conjugated antibodies are higher in the violet 450/50 channel when using UltraComp eBeads microspheres (Product # 01-2222-42) as compared to single-color stained cells. In such circumstances, we would recommend setting compensation with cells. We have also observed this in some experiments using AbC Total Antibody Compensation beads (Product # A10497).When using two or more Super Bright dye-conjugated antibodies in a staining panel, it is recommended to use Super Bright Complete Staining Buffer (Product # SB-4401) to minimize any non-specific polymer interactions. Please refer to the datasheet for Super Bright Staining Buffer for more information.Light sensitivity: This tandem dye is sensitive to photo-induced oxidation. Please protect this vial and stained samples from light.Fixation: Samples can be stored in IC Fixation Buffer (Product # 00-8222-49) (100 µL of cell sample + 100 µL of IC Fixation Buffer) or 1-step Fix/Lyse Solution (Product # 00-5333-57) for up to 3 days in the dark at 4°C with minimal impact on brightness and FRET efficiency/compensation. Some generalizations regarding fluorophore performance after fixation can be made, but clone specific performance should be determined empirically.Excitation: 405 nm; Emission: 780 nm; Laser: Violet LaserSuper Bright Polymer Dyes are sold under license from Becton, Dickinson and Company.靶标信息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, 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

Mouse IgG2a Secondary Antibody (78-4210-82) in FlowNormal human peripheral blood cells were stained with CD19 Monoclonal Antibody, FITC (Product # 11-0199-42) and unconjugated CD3 Monoclonal Antibody (Product # 14-0037-82, mouse IgG2a isotype) followed by staining with Rat Anti-Mouse IgG2a Secondary Antibody, Super Bright 780. Cells in the lymphocyte gate were used for analysis.
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