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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant Human Borealin protein (1-280AA)
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性:
Polyclonal
- 标记物:
Non-conjugated
- 适应物种:
Human
- 保质期:
6个月
- 抗原来源:
Homo sapiens (Human)
- 目录编号:
Q53HL2
- 级别:
优
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 宿主:
Rabbit
- 应用范围:
ELISA, IHC; Recommended dilution: IHC:1:20-1:200
- 浓度:
>95%,Antigen Affinity Purified
- 靶点:
CDCA8
- 抗体英文名:
CDCA8 Antibody
- 抗体名:
Pluripotent embryonic stem cell-related gene 3 protein antibody
- 规格:
100μl/50μl/20μl
| 规格: | 100μl | 产品价格: | ¥1320.0 |
|---|---|---|---|
| 规格: | 50μl | 产品价格: | ¥880.0 |
| 规格: | 20μl | 产品价格: | ¥440.0 |
保存缓冲液
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.功能
Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. In the complex, it may be required to direct the CPC to centromeric DNA. Major effector of the TTK kinase in the control of attachment-error-correction and chromosome alignment.风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Gene Targeting Vector Design for Embryonic Stem Cell Modifications
while transgenes are designed to express proteins that are normally absent from the organism. For example, gene targeting in mouse embryonic stem cells can be used to generate a mutant mouse model that fails to express a physiologically important protein
Gene Silencing in Mouse Embryonic Stem Cells
Embryonic stem cells (ESCs) are promising tools for regenerative medicine as well as for biotechnological research. However, to exploit ESCs for clinical purposes, a better understanding of the molecular mechanisms that control
Gene Targeting in Embryonic Stem Cells
Genetic modification of mouse embryonic stem cells is a powerful method to study gene function in whole animal models. The ability to re-design genes in mouse to reproduce genetic defects found in human patients gives researchers a wide open
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