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艾德科技（北京）有限公司

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表观遗传学（m6A RNA甲基化、RNA甲基化、DNA甲基化、DNA羟甲基、DNA甲酰基、DNA羧基），分子生物学，免疫生物学（一抗、二抗），细胞生物学，实验仪器学（核酸提起仪、超微量分光光度计）等等产品与技术服务

北京市昌平区中关村生命科学园东60米艾德园

联系人: Peter Chen / 邮箱: 1951545998@qq.com / QQ: 1513545070 / 电话: 0313-5935521 / 手机: 18911529660

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[商家供应] 测定总体RNA中m6A RNA甲基化-m6A RNA甲基化定量检测试剂盒（荧光法）（A-P-9008）

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现货---m6A RNA甲基化定量检测试剂盒（荧光法）货号：A-P-9008

EpiQuik m6A RNA Methylation Quantification Kit (Fluorometric)

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背景资料：N6-methyladenosine (m6A) is the most common and abundant modification on RNA molecules present in eukaryotes. The m6A modification is catalyzed by a methyltransferase complex METTL3 and removed by the recently discovered m6A RNA demethylases FTO and ALKBH5, which catalyze m6A demethylation in an α-ketoglutarate (α-KG)- and Fe2+-dependent manner. It was shown that METTL3, FTO and ALKBH5 play important roles in many biological processes, ranging from development and metabolism to fertility. m6A accounts for more than 80% of all RNA base methylations and exists in various species. m6A is mainly distributed in mRNA and also occurs in non-coding RNA such as tRNA, rRNA and snRNA. The relative abundance of m6A in mRNA transcripts has been shown to affect RNA metabolism processes such as splicing, nuclear export, translation ability and stability and RNA transcription. Abnormal m6A methylation levels induced by defects in m6A RNA methylase and demethylase could lead to dysfunction of RNA and cause disease. For example, abnormally low levels of m6A in target mRNAs due to increased FTO activity in patients with FTO mutations, through an as-yet undefined pathway, contributes to the onset of obesity and related diseases. The dynamic and reversible chemical m6A modification on RNA may also serve as a novel epigenetic marker of profound biological significance. Therefore, more useful information for better understanding of m6A RNA methylation levels and distribution on RNA transcripts could benefit diagnostics and therapeutics of disease。

产品描述：This kit contains all reagents necessary for the quantification of m6A in RNA. In this assay, total RNA is bound to strip wells using RNA high binding solution. m6A is detected using capture and detection antibodies. The detected signal is enhanced and then quantified fluorometrically by reading the RFU (relative fluorescence units) with a fluorescence spectrophotometer. The amount of m6A is proportional to the fluorescence intensity measured。

产品特点：

1·Fluorometric assay with easy-to-follow steps for convenience and speed. The entire procedure can be completed within 3 hours and 45 minutes；

2·High sensitivity, of which the detection limit can be as low as 5 pg of m6A；

3.Unique binding solution allows that RNA >70 nts can be tightly bound to the wells, which enables quantification of m6A from both mRNA and nc-RNA such as tRNA, rRNA and snRNA.
4.Optimized antibody and enhancer solutions allow high specificity to m6A, with no cross-reactivity to unmethylated adenosine within the indicated concentration range of the sample RNA；

5.Universal positive and negative controls are included, which are suitable for quantifying m6A from any species；

6.Strip-well microplate format makes the assay flexible for manual or high throughput analysis；

7.Simple, reliable, and consistent assay conditions；

8.Flexible - Strip-well microplate format makes the assay available for manual or high throughput analysis。
更多产品详情，请参考链接：https://www.aderr.com/cn/main.php?m=1346&t=5507&id=57271
同时，还有配套的RNA提取试剂盒推荐哦！还能吃到正宗的内蒙古大草原的奶酪！小盆友，再也不犹豫了！