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Merck
CN

MAB3560

抗 8-氧鸟嘌呤抗体,克隆 483.15

ascites fluid, clone 483.15, Chemicon®

别名:

8-oxoG

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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

mouse

质量水平

抗体形式

ascites fluid

抗体产品类型

primary antibodies

克隆

483.15, monoclonal

种属反应性

monkey, human, primate

种属反应性(根据同源性预测)

mouse, rat

制造商/商品名称

Chemicon®

技术

ChIP: suitable
ELISA: suitable
immunocytochemistry: suitable

同位素/亚型

IgM

运输

dry ice

靶向翻译后修饰

unmodified

基因信息

human ... OGG1(4968)

一般描述

8-氧桥鸟嘌呤是鸟嘌呤的诱变氧化损伤产物。由于细胞中存在活性氧,因此在所有活生物体的DNA中都会产生氧化损伤的碱基8-氧桥鸟嘌呤。DNA损伤威胁着储存在每个DNA分子中的遗传信息的健康;然而,细胞中存在酶以防止这种病变的诱变作用。8-氧桥鸟嘌呤是由氧化应激产生的最丰富和特征最充分的DNA损伤之一。据估计,每个哺乳动物细胞每天约有180个鸟嘌呤被氧化为8-oxoG。8-oxoG是一种错误编码的病变,可导致G:C变为 T:A或 T:A变为G:C颠换突变。随着年龄的增长,这种病变会在DNA中积累,并且与多种癌症和疾病(例如阿尔茨′海默氏症和帕金森′氏症)紧密相关。

免疫原

吸附在氧化铝上的8-氧桥鸟嘌呤

应用

免疫细胞化学:
在多聚甲醛固定的HeLa和Cos7细胞上。8-氧桥鸟嘌呤已定位于营养缺乏细胞的细胞核。

ELISA:
在载玻片上生长的细胞用冷的560nM NaCl;0.1%(v/v)Triton X-100;0.02%(w/v)SDS;10mM磷酸盐缓冲液pH 7.4提取两次,每次30秒,并用新鲜制备的4% PFA固定在室温下5-20分钟。{Conlon,KA et al(2000)J. Histotechnology 23(1):37-44}。典型的染色表明,提取细胞的细胞核具有确定的染色质浓缩外围和区域。克隆483.15染色在补充DMEM中孵育的细胞中显示出特异性但微弱的核荧光染色,但在无营养的定义盐溶液(NFDSS){1.8mM氯化钙、110mM NaCl、44mM碳酸氢钠,pH 7.5}中孵育的细胞中显示出强烈的核荧光染色,呈点状并呈一般分布。即使在最初的NFDSS处理后,在营养培养基中孵育的细胞中,荧光染色也会消失至背景水平{Conlon等人}。

该抗体的一个先前批次被用于ELISA测定。

最佳工作稀释度必须由最终用户确定。
抗8-氧桥鸟嘌呤抗体(克隆483.15)可检测8-氧桥鸟嘌呤水平,&已发布&验证可用于ELISA&IC。

生化/生理作用

8-氧桥鸟嘌呤。通过竞争性ELISA,单克隆抗体在微摩尔浓度下与dGMP、dAMP、dCMP或TMP没有反应性。仅当浓度增加到毫摩尔范围时才观察到竞争。

外形

未纯化的小鼠单克隆IgM液体,溶于不含防腐剂的缓冲液中。

制备说明

自收到之日起,以未稀释的等分试样可于-20ºC条件下稳定保存6个月。
处理建议:接收后,在取下盖子之前,离心小瓶并轻轻混合溶液。分装至微量离心管中,并储存于-20°C。避免反复冻融循环,否则可能损坏IgM并影响产品性能。

分析说明

对照
营养缺乏的HeLa或Cos7细胞
通过免疫细胞化学对NIH/3T3细胞进行常规评估

免疫细胞化学:
使用抗8-氧桥鸟嘌呤小鼠单克隆抗体对NIH/3T3细胞进行共聚焦荧光分析。

其他说明

浓度:关于批次特定浓度请参见检验报告。

法律信息

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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储存分类代码

10 - Combustible liquids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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