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53BP1 Recombinant Rabbit Monoclonal Antibody (7H14L12), Alexa Fluor™ Plus 555

类型:流式抗体
品牌:Thermo Fisher
种属:Human
应用:Flow,ICC/IF
抗体亚型:IgG
偶联物:Alexa Fluor Plus 555/AFP555
宿主:Rabbit
克隆号:7H14L12
浓度:1 mg/mL

规格: 20 μL

货号: 703580RP555XS

价格: ¥2400.00

优惠: ¥1680.00

规格: 50 μL

货号: 703580RP555

价格: ¥3890.00

优惠: ¥2723.00

数量:

应用

建议稀释比

免疫细胞化学 (ICC/IF)

1:100 - 1:200

流式细胞分析 (Flow)

0.06-0.5 µg/test

 

产品详细信息

 

Alexa Fluor™ Plus recombinant antibodies are conjugated using new, proprietary dye chemistry so you can generate stunning data. Alexa Fluor™ Plus antibodies represent an advancement in fluorescent conjugate technology. Alexa Fluor™ Plus antibodies provide brighter signal compared to leading Alexa Fluor™ antibodies, providing you with better signal-to-noise for your critical experiments. These antibodies show better specificity and lot-to-lot consistency as these are recombinant antibodies, generated by cloning specific genes for the desired antibodies into an expression vector and expressed in vitro.

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.

Applications Tested: This 53BP1 antibody has been tested by immunocytochemistry and flow cytometric analysis of HeLa cells. This may be used for immunocytochemistry at 5 µg/mL and for flow cytometry at less than or equal to 0.25 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.

Excitation: 553 nm; Emission: 568 nm; Laser: Yellow Laser

Filtration: 0.2 µm post-manufacturing filtered.

 

靶标信息

 

53BP1 (P53-binding protein 1) plays a critical role in tumor suppression and is a putative substrate of ATM kinase. Upon DNA damage, 53BP1 is phosphorylated and localizes to the presumptive sites of damage, specifically, double-strand breaks. 53BP1 may have a role in checkpoint signaling during mitosis, enhances TP53-mediated transcriptional activation, and participates in DNA repair by maintaining genomic stability.

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