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Invitrogen
Rat anti-Mouse IgG1 Secondary Antibody, eFluor™ 450, eBioscience™
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Mouse IgG1 Secondary Antibody (48-4015-82) in Flow
Staining of normal human peripheral blood cells with staining buffer (blue histogram) or Anti-Human CD4 Purified (clone SK3, a mouse IgG1, Product # 14-0047) (purple histogram) followed by 0.25 µg of Anti-Mouse IgG1 eFluor® 450. Cells in the lymphocyte gate were used for analysis.
产品信息
48-4015-82
应用
建议稀释比
流式细胞分析 (Flow)
0.5 µg/test
产品规格
种属反应
Mouse
宿主/亚型
Rat
/ IgG
分类
Monoclonal
类型
Secondary Antibody
克隆号
M1-14D12
偶联物
激发/发射光谱
405/445 nm
查看光谱
形式
Liquid
浓度
0.2 mg/mL
纯化类型
Affinity chromatography
保存液
PBS, pH 7.2
内含物
0.09% sodium azide
保存条件
4° C, store in dark, DO NOT FREEZE!
运输条件
Ambient (domestic); Wet ice (international)
RRID
AB_2574060
靶标
IgG1
抗体形式
Whole Antibody
产品详细信息
Description: The monoclonal antibody M1-14D12 recognizes Mouse IgG1 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 IgG1 or any rat isotype antibodies.
Applications Reported: The 1C10 antibody has been reported for use in flow cytometric analysis.
Applications Tested: This M1-14D12 antibody has been tested by flow cytometric analysis of staining with a mouse IgG1 primary antibody. This can be used at less than or equal to 0.5 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.
eFluor® 450 is an alternative to Pacific Blue®. eFluor® 450 emits at 445 nm and is excited with the Violet laser (405 nm). Please make sure that your instrument is capable of detecting this fluorochome.
Excitation: 405 nm; Emission: 445 nm; Laser: Violet Laser.
Filtration: 0.2 µm post-manufacturing filtered.
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, 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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