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Merck
CN

ABE364

抗-Tet2抗体

from rabbit, purified by affinity chromatography

别名:

Methylcytosine dioxygenase TET2

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

纯化方式

affinity chromatography

种属反应性

mouse, human, rat

技术

immunocytochemistry: suitable
immunohistochemistry: suitable (paraffin)
western blot: suitable

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... TET2(54790)

一般描述

甲基胞嘧啶双加氧酶TET2催化甲基胞嘧啶(5mC)向5-羟甲基胞嘧啶(5hmC)的转化。目前尚不清楚5-羟甲基胞嘧啶的功能,但它可能影响染色质结构,或充当胞嘧啶去甲基化的中间成分。TET2在骨髓增生性疾病(MPD)或骨髓增生性肿瘤(MPN)和全身性肥大细胞增生症中经常发生突变。TET2紊乱还会导致真性红细胞增多症(PV)和骨髓异常增生综合征(MDS)。
观察值〜140 kDa。已知存在223 kDa(亚型1),133 kDa(亚型2)和133 kDa(亚型3)的三个亚型。该抗体应基于序列同源性识别全部三种亚型。在某些细胞裂解物中,在〜36 kDa处可能观察到未表征的条带。(注意:亚型2和3可能在低浓度下观察到,而亚型1可能在某些细胞裂解物中以较高浓度检测到。)

免疫原

KLH偶联线性肽对应于人Tet2。

应用

免疫组化分析:代表性批次的1:4,000稀释液在鼠髓质组织中检测到Tet2。

免疫细胞化学分析:代表性批次的1:100稀释液在人H9胚胎干细胞中检测到Tet2。
抗-Tet2可检测Tet2蛋白的水平&已发表&经验证可用于WB,IHC& ICC。

分析说明

通过蛋白质印迹在小鼠胚胎干细胞中进行了评估。

蛋白质印迹分析:1 µg/mL该抗体在10 µg小鼠胚胎干细胞中检测到Tet2。(注意:在低浓度或更长暴露时间下可观察到亚型2和3,而在某些细胞裂解液中可在更高浓度或更长暴露时间下检测到亚型1)。

其他说明

浓度:请参考批次特异性浓缩物的分析证书。

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

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Journal of hematology & oncology, 14(1), 83-83 (2021-05-28)
Challenges remain on the selection of patients who potentially respond to a class of drugs that target epigenetics for cancer treatment. This study aims to investigate TET2/DNMT3A mutations and antitumor activity of a novel epigenetic agent in multiple human cancer
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DNA hydroxylation catalyzed by Tet dioxygenases occurs abundantly in neurons in mammals. However, effects of ten-eleven translocation methylcytosine dioxygenase 1 (TET1) expression and hydroxymethylation status on neuron injury remain unclear. This study was designed to explore the effects of TET1
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Cerebral palsy (CP) is a neurodevelopmental disorder usually occurring early in life and persisting through the whole life. Several risk factors, including perinatal hypoxia-ischemia (HI), may contribute to occurrence of CP in preterm infants. DNA hydroxymethylation has been shown to

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