In Vivo Grade Recombinant Anti
-mouse PD-L1 Mouse IgG2a Kappa Monoclonal Antibody (Clone 10F.9G2.1)- ￥5950
- Syd Labs
- 美国
- PA007164.m2a
- 2026年01月09日
- ELISA, WB, Flow cytometry, IHC, ICC, animal model study
- Mouse
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
The original rat hybridoma (clone name: 10F.9G2) was generated by immunizing rats with the mouse PD-L1 cDNA and mouse PD-L1 CHO transfectants.
- 亚型：
Mouse IgG2a Kappa
- 形态：
Liquid
- 保存条件：
Store at 2-8℃ and protected from prolonged exposure to light. Avoid freeze/thaw cycles.
- 克隆性：
Monoclonal Antibody
- 适应物种：
Mouse
- 保质期：
如果保存在2 至 8°C，自收到之日起可保存1个月。如果保存在-20 至 -70°C，自收到之日起可保存 12个月。
- 抗原来源：
The original rat hybridoma (clone name: 10F.9G2) was generated by immunizing rats with the mouse PD-L1 cDNA and mouse PD-L1 CHO transfectants.
- 库存：
3 weeks
- 供应商：
青木生物技术（武汉）有限公司
- 宿主：
Mouse
- 应用范围：
ELISA, WB, Flow cytometry, IHC, ICC, animal model study
- 浓度：
以实际发货为准
- 靶点：
PD-L1
- 抗体英文名：
In Vivo Grade Recombinant Anti-mouse PD-L1 Mouse IgG2a Kappa Monoclonal Antibody (Clone 10F.9G2.1)
- 抗体名：
In Vivo Grade Recombinant Anti-mouse PD-L1 Mouse IgG2a Kappa Monoclonal Antibody (Clone 10F.9G2.1)
- 规格：
5mg
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文献和实验Rapid Isotyping of Mouse Monoclonal Antibodies
from serum, valence, and avidity, all depend on isotype. Isotyping is a basis for the selection of antibody purification, conjugation, fragmentation, and storage procedures, and predicts cytotoxic properties and half-life in vivo (see Note 1 ). In addition
Production of Monoclonal Antibody by DNA Immunization with Electroporation
construct was injected intramuscularly with in vivo electroporation into mice, and the specific antibody production in mice was analyzed by enzyme-linked immunosorbent assay (ELISA). Hybridomas were generated by fusing mouse splenocytes with myeloma cells
【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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