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重要文件

ABE572

Sigma-Aldrich

抗N6-甲基腺苷(m6A)抗体

from rabbit

同義詞:

m6A

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

rabbit

抗體表格

purified antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

物種活性(以同源性預測)

all

技術

ChIP: suitable
RIP: suitable
dot blot: suitable

運輸包裝

wet ice

目標翻譯後修改

unmodified

一般說明

N6-甲基腺苷(m6A),或腺苷N6位的甲基化,是RNA的一种转录后修饰。 由于分析方法的缺乏,人们对N6-甲基腺苷了解的很少,但新证据表明它是一种非常常见的碱基修饰和重要的生理调节因子。N6-甲基腺苷在整个大脑发育过程中都会显著增加,并会在终止密码子、microRNA结合位点和UTR附近富集,表明了其在基因表达调节中的基础性作用。N6-甲基腺苷在人和小鼠之间也高度保守。

免疫原

BSA偶联的N6-甲基腺苷。

應用

染色质免疫沉淀分析:A representative lot from an independent laboratory detected N6-methyladenosine in RNA containing N6-methyladenosine (Dominissini, D., et al. (2012).Nature.485(7397):201-206.; Meyer, K. D., et al. (2012).Cell.149(7):1635-1646.).

(RNA) Immunoprecipitation Analysis: A representative lot from an independent laboratory detected N6-methyladenosine in methylated RNA containing N6-methyladenosine (Meyer, K. D., et al. (2012).Cell.149(7):1635-1646.).

Dot Blot Analysis: A representative lot from an independent laboratory detected N6-methyladenosine in a panel of modified oligonucleotides (Meyer, K. D., et al. (2012).Cell.149(7):1635-1646.; Jia, G., et al. (2011).Nat Chem Biol. 7(12):885-887.).
研究子类别
染色质生物学
研究类别
表观遗传学&核功能
通过使用已验证用于斑点印迹、染色质IP(ChIP) & RNA结合蛋白IP(RIP)的抗-N6-甲基腺苷(m6A)抗体检测N6-甲基腺苷(m6A)。

品質

已通过斑点印迹在含有N6-甲基腺苷的低聚物中进行评估。

斑点印迹分析: 1 µg/mL的该抗体可在含有N6-甲基腺苷的低聚物中检测到N6-甲基腺苷。

外觀

在含有0.05%叠氮化钠PBS的缓冲液中的纯化兔多抗。
形式:纯化
纯化的蛋白 A

儲存和穩定性

自发运之日起,在 2-8°C 条件下可稳定保存1年

其他說明

浓度:请参考批次特异性浓缩物的分析证书。

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Karolos Douvlataniotis et al.
Science advances, 6(12), eaay3335-eaay3335 (2020-03-25)
N6-methyladenine (6mdA) is a widespread DNA modification in bacteria. More recently, 6mdA has also been characterized in mammalian DNA. However, measurements of 6mdA abundance and profiles are often very dissimilar between studies, even when performed on DNA from identical mammalian
Comprehensive analysis of mRNA methylation reveals enrichment in 3' UTRs and near stop codons.
Meyer, Kate D, et al.
Cell, 149, 1635-1646 (2012)
Xiaoling Liu et al.
Analytical chemistry, 90(9), 5546-5551 (2018-04-14)
N6-methyladenine (6mA) is a rediscovered DNA modification in eukaryotic genomes. To explore the distribution and functions of 6mA, it is of paramount option to use immunoprecipitation to select 6mA-containing DNA fragments for genome-wide sequencing. Presumably, most of the 6mA-free fragments
Jiyu Tong et al.
Science advances, 7(18) (2021-04-30)
m6A RNA modification is implicated in multiple cellular responses. However, its function in the innate immune cells is poorly understood. Here, we identified major m6A "writers" as the top candidate genes regulating macrophage activation by LPS in an RNA binding
Guifang Jia et al.
Nature chemical biology, 7(12), 885-887 (2011-10-18)
We report here that fat mass and obesity-associated protein (FTO) has efficient oxidative demethylation activity targeting the abundant N6-methyladenosine (m(6)A) residues in RNA in vitro. FTO knockdown with siRNA led to increased amounts of m(6)A in mRNA, whereas overexpression of

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