推荐产品
生物来源
mouse
质量水平
偶联物
unconjugated
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
195C, monoclonal
表单
buffered aqueous solution
分子量
antigen ~167 kDa
种属反应性
human
浓度
~1 mg/mL
技术
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
western blot: 2-4 μg/mL using nuclear cell extract of HeLa cells
同位素/亚型
IgG1
UniProt登记号
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... WRN(7486)
一般描述
抗WRN小鼠单克隆抗体（小鼠IgG1亚型）是由小鼠骨髓瘤细胞（p3-NS1/Ag4-1）和用制备自人WRN重组融合蛋白片段进行免疫的BALB/c小鼠脾细胞融合产生的杂交瘤195C生成的。Werner综合征ATP依赖性解旋酶（WRN）位于8号染色体上，为167 kDa。WRN蛋白属于DNA解旋酶的RecQ解旋酶家族。
免疫原
人WRN的重组融合蛋白片段（氨基酸1074-1432）。
应用
WRN抗体还可用于
- 酶联免疫吸附测定（ELISA）
- 免疫印迹
- 免疫沉淀
- 免疫组化
- 蛋白印迹
生化/生理作用
Werner综合征ATP依赖性解旋酶（WRN）蛋白已被证明具有三种已知的催化活性：3′-5′ 解旋酶、核酸外切酶和ATP酶活性。该蛋白的C端区域包含核定位信号（NLS），因此将WRN蛋白靶向细胞核，核仁和核质灶。WRN参与多种DNA代谢过程表明其具有抑癌作用。WRN蛋白的突变会导致Werner综合征（WS）。WRN的表观遗传失活导致WRN-核酸外切酶活性丧失，导致染色体不稳定性增加和对化疗药物的超敏反应。
外形
0.01M 磷酸缓冲盐溶液，pH 7.4，含 15mM 叠氮化钠。
免责声明
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。
未找到合适的产品？
试试我们的产品选型工具.
储存分类代码
10 - Combustible liquids
WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
常规特殊物品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Class I histone deacetylase HDAC1 and WRN RECQ helicase contribute additively to protect replication forks upon hydroxyurea-induced arrest
Kehrli K, et al.
The Journal of Biological Chemistry, 291(47), 24487-24503 (2016)
Yuyao Tian et al.
Cell & bioscience, 14(1), 7-7 (2024-01-07)
Metabolic dysfunction is one of the main symptoms of Werner syndrome (WS); however, the underlying mechanisms remain unclear. Here, we report that loss of WRN accelerates adipogenesis at an early stage both in vitro (stem cells) and in vivo (zebrafish).
Bidisha Saha et al.
Molecular genetics & genomic medicine, 1(1), 7-14 (2013-08-13)
Werner syndrome is a rare autosomal recessive disorder characterized by multiple features consistent with accelerated aging. It is caused by mutations in the WRN gene, which encodes a RecQ type helicase. To date, more than 70 disease-causing mutations have been
S Deepak Amalnath et al.
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 36(4), 323-325 (2017-08-11)
Werner syndrome is a rare progeroid syndrome caused by the WRN gene mutation. It is characterized by a general appearance of premature aging, diabetes mellitus, and atherosclerosis, and an increased risk of malignancies. We report a patient who presented with
Linda J W Bosch et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 22(18), 4612-4622 (2016-04-29)
WRN promoter CpG island hypermethylation in colorectal cancer has been reported to increase sensitivity to irinotecan-based therapies. We aimed to characterize methylation of the WRN promoter, determine the effect of WRN promoter hypermethylation upon expression, and validate a previous report
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门