| 查看: 364 | 回复: 29 | ||
| 【有奖交流】积极回复本帖子,参与交流,就有机会分得作者 ADTechnology 的 83 个金币 ,回帖就立即获得 1 个金币,每人有 1 次机会 | ||
| 当前只显示满足指定条件的回帖,点击这里查看本话题的所有回帖 | ||
ADTechnology
|
[商家供应]
m6A RNA甲基化片段富集试剂盒【qPCR版】-(A-P-9018)【长期现货供应】
|
|
m6A RNA甲基化片段富集试剂盒---非常适合qPCR检测单个位点 货号:A-P-9018EpiQuik CUT&RUN m6A RNA Enrichment Kit 背景资料:N6-methyl-adenosine (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 m6A RNA demethylases FTO and ALKBH5, which catalyze m6A demethylation in an α-ketoglutarate (α-KG)- and Fe2+-dependent manner. METTL3, FTO, and ALKBH5 are known to 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 a better understanding of m6A RNA methylation levels and distribution on RNA transcripts could benefit diagnostics and therapeutics of disease。 产品描述:Kit contains all necessary reagents required for carrying out a successful m6A RNA enrichment starting from total RNA. In the reaction, RNA sequences in both ends of the target m6A-containing regions are cleaved/removed and the target m6A-containing fragments are pulled down using a beads-bound m6A capture antibody. The enriched RNA is then released, purified and eluted. Included in the kit are a non-immune IgG control and m6A positive control. These can be used to demonstrate the efficacy of the kit and performance at the enriched RNA quantification or bioanalyzer step。 产品特点: 1·High enrichment: Uses an RNA cleavage enzyme mix to simultaneously fragment RNA and cleave/remove any RNA sequences in both ends of the target m6A-containing sequences without affecting RNA regions occupied by the antibody. Short RNA fragments are generated only bound with anti- m6A antibody. True target m6A-enriched regions can, therefore, be reliably identified, and high-resolution mapping achieved; 2·Low input: Unbound RNA cleavage and immunocapture are processed in the same single-tube, which enables maximum protection of the target m6A-containing regions and minimized sample loss, allowing the input RNA to be as low as 500 ng; 3.Minimal Background: Cleavage of unbound RNA sequences in the two (2) ends of the target m6A-containing sequences enables minimized MeRIP/sequencing background, allowing data analysis with <10 million reads. 4.Fast, streamlined procedure: The procedure from RNA to library cDNA is less than 3 hours with <30 min of hands-on time; 5.Highly convenient: The kit contains all required components for each step of the EpiQuik™ CUT&RUN m6A RNA Enrichment Kit, which are sufficient for m6A-containing RNA sequence capture, thereby allowing CUTARUNTM m6A RNA enrichment to be the most convenient with reliable and consistent results。 更多请参考:https://www.aderr.com/cn/main.ph ... 07&id=57807 p-9018-05.png |
» 本帖附件资源列表
-
欢迎监督和反馈:小木虫仅提供交流平台,不对该内容负责。
本内容由用户自主发布,如果其内容涉及到知识产权问题,其责任在于用户本人,如对版权有异议,请联系邮箱:xiaomuchong@tal.com - 附件 1 : A-P-9018-m6A_RNA甲基化片段富集试剂盒.pdf
2020-06-01 11:27:54, 780.33 K
» 猜你喜欢
求助:我三月中下旬出站,青基依托单位怎么办?
已经有6人回复
北京211副教授,35岁,想重新出发,去国外做博后,怎么样?
已经有8人回复
Cas 72-43-5需要30g,定制合成,能接单的留言
已经有7人回复
磺酰氟产物,毕不了业了!
已经有5人回复
论文终于录用啦!满足毕业条件了
已经有25人回复
2026年机械制造与材料应用国际会议 (ICMMMA 2026)
已经有3人回复
自荐读博
已经有3人回复
不自信的我
已经有5人回复
投稿Elsevier的杂志(返修),总是在选择OA和subscription界面被踢皮球
已经有8人回复
» 抢金币啦!回帖就可以得到:
求一个访问学者邀请函,非常非常感谢
+1/684
博士去军队文职怎么样
+5/355
双一流南京医科大学招计算机、AI、统计、生物信息等方向26年9月入学博士
+1/180
供应德国EXAKT艾卡特半导体导热散热材料三辊研磨机50 PLUS
+1/94
中国石油大学(华东)电气工程专业博士研究生招生
+1/86
湖南师范大学医工交叉科研团队招收计算机博士生
+1/86
山东征女友,坐标济南
+1/63
考核制博士自荐
+1/40
华中科技大学龚江研究员课题组诚招博士研究生、科研助理和博士后
+2/32
厦门大学航空航天学院智能制造课题组招2026年申请审核制博士生1-2名
+1/31
西北工业大学无人飞行器技术全国重点实验室拟招收电机/自动化方向博士1~2名
+1/30
可以用同一个研究内容申请青C和博士后面上吗
+1/25
吉林大学材料物理本科生求问调剂信息
+1/11
求博导收留
+1/5
浙江大学傅杰团队(杰青)高薪招聘博士后
+1/5
中国科学院苏州纳米所院士团队博士后岗位招聘
+1/4
中科院动物所招收2026年博士生(优先少干专项计划、化学或生命科学背景)
+1/4
废旧塑料热解油采购
+1/2
乙酸乙酯如何除丙烯酸甲酯
+1/2
层流压差质量流量计在电解水制氢中的应用
+1/1
3楼2020-06-01 11:36:20
ADTechnology 
捐助贵宾 (著名写手)
2楼2020-06-01 11:32:03
danghaha
新虫 (文坛精英)
- 应助: 0 (幼儿园)
- 金币: 4397.4
- 散金: 41604
- 红花: 66
- 沙发: 7
- 帖子: 41672
- 在线: 340.9小时
- 虫号: 4692823
- 注册: 2016-05-15
- 性别: MM
- 专业: 信号理论与信号处理
4楼2020-06-01 13:00:06
6楼2020-06-02 14:11:11


m6A RNA甲基化片段富集试剂盒---非常适合qPCR检测单个位点 货号:A-P-9018
回复此楼