生物来源
mouse
质量水平
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
280-5F-4E-5E, monoclonal
种属反应性
human
制造商/商品名称
Chemicon®
技术
immunofluorescence: suitable
同位素/亚型
IgG2a
运输
wet ice
应用
IFA为1:1000。 用含蛋白质的缓冲液(pH 7.5-8.0)或其他稳定介质稀释。 最终工作稀释度必须由最终使用者进行确定。
抗柯萨奇病毒B3抗体,克隆280-5F-4E-5E是用于IF的抗柯萨奇病毒B3的抗体。
研究子类别
传染病 - 病毒
传染病 - 病毒
研究类别
传染病
传染病
生化/生理作用
与柯萨奇病毒B3反应。 以1:6,000滴度中和柯萨奇病毒B3Nancy株。
外形
形式:纯化
纯化的免疫球蛋白。 溶于0.02M PB,0.25M NaCl(pH 7.6)和0.1%叠氮化钠。
制备说明
维持在2-8°C。
其他说明
浓度:请参考批次特异性浓缩物的检验报告。
法律信息
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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人类或动物食用或应用。
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储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Yanhong Wei et al.
Molecules (Basel, Switzerland), 25(6) (2020-03-25)
Coxsackievirus B3 (CVB3) is the most common cause of acute and chronic viral myocarditis, primarily in children, while human adenovirus infections represent a significant cause of morbidity and mortality worldwide, in people of all ages. A series of novel 2-benzoxyl-phenylpyridine
Enteroviral infections in children with malignant disease: a 5-year study in a single institution.
Maria A Moschovi, Katerina Katsibardi, Maria Theodoridou, Athanassios G Michos et al.
The Journal of Infection null
Coxsackievirus B3 sequences in the myocardium of fatal cases in a cluster of acute myocarditis in Greece.
Spanakis, N; Manolis, EN; Tsakris, A; Tsiodras, S; Panagiotopoulos, T; Saroglou, G; Legakis, NJ
Journal of Clinical Pathology null
Xiang Liu et al.
Scientific reports, 9(1), 10656-10656 (2019-07-25)
The Muc-1 oncoprotein is a tumor-associated mucin often overexpressed in pancreatic cancer. We report that knockout of Muc-1 reduced the degree of pancreatic inflammation that resulted from infection with Coxsackievirus B3 (CVB3) in a mouse model. CVB3-infected Muc-1-deficient (Muc-1KO) mice
Wenchun Fan et al.
Cell, 184(13), 3410-3425 (2021-06-02)
To control viral infection, vertebrates rely on both inducible interferon responses and less well-characterized cell-intrinsic responses composed of "at the ready" antiviral effector proteins. Here, we show that E3 ubiquitin ligase TRIM7 is a cell-intrinsic antiviral effector that restricts multiple
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