Anti-HSV2 ICP8 Major DNA binding蛋白抗体[4E6] (ab6515)
Key features and details
- Mouse monoclonal [4E6] to HSV2 ICP8 Major DNA binding protein
- Suitable for: WB, ELISA, ICC/IF
- Reacts with: Human herpesvirus 2
- Isotype: IgG2a
概述
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产品名称
Anti-HSV2 ICP8 Major DNA binding蛋白抗体[4E6] -
描述
小鼠单克隆抗体[4E6] to HSV2 ICP8 Major DNA binding蛋白 -
宿主
Mouse -
经测试应用
适用于: WB, ELISA, ICC/IFmore details -
种属反应性
与反应: Human herpesvirus 2 -
免疫原
Herpes Virus
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常规说明
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
性能
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形式
Liquid -
存放说明
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles. -
存储溶液
pH: 7.4 -
Concentration information loading...
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纯度
Protein A purified -
克隆
单克隆 -
克隆编号
4E6 -
骨髓瘤
NS1/1-Ag4-1 -
同种型
IgG2a -
轻链类型
kappa -
研究领域
相关产品
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Compatible Secondaries
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Isotype control
应用
应用 | Ab评论 | 说明 |
---|---|---|
WB |
Use at an assay dependent concentration.
> 1:16,000 |
|
ELISA |
Use at an assay dependent concentration.
0.100 @ >1:102,400 |
|
ICC/IF |
Use at an assay dependent concentration.
1+ @ 1:12,800. |
说明 |
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WB
Use at an assay dependent concentration. > 1:16,000 |
ELISA
Use at an assay dependent concentration. 0.100 @ >1:102,400 |
ICC/IF
Use at an assay dependent concentration. 1+ @ 1:12,800. |
靶标
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相关性
ICP8 (Infected cell protein 8)is the major DNA binding protein of herpes simplex virus type 2. It is single stranded and is required for DNA replication. -
细胞定位
Nuclear -
别名
- DBP antibody
- Herpes simplex virus 2 antibody
- Human herpesvirus 2 antibody
see all
实验方案
数据表及文件
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Datasheet download
文献 (0)
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