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- CUSABIO
- CN
- CSB-RA019025A542phHU
- 2025年07月12日
- ELISA, WB, IP; Recommended dilution: WB:1:500-1:5000, IP:1:200-1:1000
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
A synthesized peptide derived from human Phospho-PTPN11 (Y542)
- 亚型：
Rabbit IgG
- 形态：
liquid
- 保存条件：
store at -20°C or -80°C.
- 克隆性：
Monoclonal
- 标记物：
Non-conjugated
- 适应物种：
Human
- 保质期：
12
- 抗原来源：
Human
- 目录编号：
2E2
- 级别：
优
- 库存：
99
- 供应商：
武汉华美生物/CUSABIO
- 宿主：
Rabbit
- 应用范围：
ELISA, WB, IP; Recommended dilution: WB:1:500-1:5000, IP:1:200-1:1000
- 浓度：
参见官网
- 靶点：
PTPN11
- 抗体英文名：
Phospho-PTPN11 (Y542) Antibody
- 抗体名：
Tyrosine-protein phosphatase non-receptor type 11, Protein-tyrosine phosphatase 1D, PTP-1D, Protein-tyrosine phosphatase 2C, PTP-2C, SH-PTP2, SHP-2, Shp2, SH-PTP3, PTPN11, PTP2C, SHPTP2
- 规格：
100ul / 50ul
PTPN11|PTPN11抗体|Phospho-PTPN11 (Y542) Antibody|重组抗体
Uniprot ID：Q06124
宿主：Rabbit
反应种属：Human
应用：ELISA, WB, IP; Recommended dilution: WB:1:500-1:5000, IP:1:200-1:1000
别名：Tyrosine-protein phosphatase non-receptor type 11, Protein-tyrosine phosphatase 1D, PTP-1D, Protein-tyrosine phosphatase 2C, PTP-2C, SH-PTP2, SHP-2, Shp2, SH-PTP3, PTPN11, PTP2C, SHPTP2
相关咨询：参见官网/联系客服
微信ID: Cusabio01 电话： 027-87939808
详情请登录：www.cusabio.cn
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Adsroption of Anti-E. coli Antibodies Grow E. coli strain Y1090 in L broth at 37°C overnight. Transfer to 10 mM MgSO4 and store at 4°C for future use. These cells are good for about 1 week. Soak one 132 mm nitrocellulose membrane per Petri dish
Radiometal Labeling of Antibodies and Antibody Fragments for Imaging and Therapy
Monoclonal antibodies (MAbs) are highly selective agents for delivering radiation to tumors both for in vivo imaging (radioimmunoscintigraphy, RIS) and for therapy (radioimmunotherapy, RIT). Antibody-based radiopharmaceuticals can be labeled
【翻译】Development trends for monoclonal antibody cancer therapeutics
). However, since 2000, humanized and human mAbs have been entering clinical study at approximately the same rate (4.3 versus 4.5 mAbs per year, respectively). Figure 1 | Categories of monoclonal antibody cancer therapeutics entering clinical study during 1980–1989
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