| 查看: 359 | 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 | ||
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
论文终于录用啦!满足毕业条件了
已经有17人回复
不自信的我
已经有5人回复
磺酰氟产物,毕不了业了!
已经有4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:
武汉纺织大学电子与电气工程学院------院长团队招聘光电、材料类博士,博士后
+1/491
北京理工大学郑长松教授课题组诚招2026年秋季博士/硕士研究生
+3/416
限广州,征女友
+2/94
上海大学昝鹏教授、军事医学研究院伯晓晨研究员/倪铭副研究员 课题组招聘博士生
+1/88
福建师范大学柔性电子学院招收2026年博士(储能材料与柔性电子器件)
+1/85
87 年东北小哥定居苏州(沪杭亦可),诚寻携手余生的你
+1/58
国重点实验室双一流A类长江学者团队招2026年全日制博士1-2名/博后1-2名
+2/54
香港理工大学-应用生物与化学科技学系 招收2025年博士研究生
+2/50
南科大薛亚辉课题组诚聘离子输运、低维器件、原子力显微镜等方向“快响行动”博士生
+1/26
浙江大学傅杰团队(杰青)高薪招聘博士后
+1/19
南京工业大学招收2026年全日制学术博士(供热、供燃气通风与空调)
+1/11
长江学者团队招聘药学/生物信息学等方向高校教师7名(地点杭州、有事业编)+博后5名
+1/10
【博士后/科研助理招聘-北京理工大学-集成电路与电子学院-国家杰青团队】
+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
中国矿业大学黄赳课题组联合中国科学院南京土壤研究所朱晓芳研究员诚聘博士后
+1/2
英国博导招CSC博士生
+1/2
上海理工大学 生物医学工程专业 招收2026年全日制博士生一名
+1/1
&#128073;划重点!硼替佐米药物研发质控必备
+1/1
&#128073;划重点!硼替佐米药物研发质控必备
+1/1
上海大学张进教授课题组诚招2026年秋季博士研究生
+1/1
ADTechnology 
捐助贵宾 (著名写手)
2楼2020-06-01 11:32:03
3楼2020-06-01 11:36:20
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
★
ADTechnology(金币+1): 谢谢参与
ADTechnology(金币+1): 谢谢参与
|
5楼2020-06-01 14:51:51
6楼2020-06-02 14:11:11
7楼2020-06-02 14:22:17
8楼2020-06-02 14:43:24
★
ADTechnology(金币+1): 谢谢参与
ADTechnology(金币+1): 谢谢参与
|
9楼2020-06-02 14:45:25
★
ADTechnology(金币+1): 谢谢参与
ADTechnology(金币+1): 谢谢参与
|
10楼2020-06-02 19:31:15


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
