- ￥22
- ProSci
- 美国
- PSI-63-472-400ul
- 2025年07月08日
- WB, IHC-P, Flow
- 兔
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
This Cdc14 antibody is generated from rabbits immunized with a recombinant protein encoding aa 1~379 of human cdc14.
- 保存条件：
Store at 4℃ for three months and -20℃, stable for up to one year
- 保质期：
1年
- 级别：
科研级别
- 库存：
100
- 供应商：
艾美捷科技
- 宿主：
兔
- 应用范围：
WB, IHC-P, Flow
- 抗体英文名：
Cdc14 Antibody
- 抗体名：
Cdc14 Antibody
- 规格：
400ul
Cdc14 抗体，Cdc14 Antibody，Cdc14 抗体,Cdc14 Antibody
产品名称：Cdc14 抗体-Cdc14 Antibody
产品货号：PSI-63-472-400ul
产品规格：400ul
背景资料：The protein encoded by this gene is a member of the dual specificity protein tyrosine phosphatase family. This protein is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit of cell mitosis and initiation of DNA replication, which suggests the role in cell cycle control. This protein has been shown to interact with and dephosphorylates tumor suppressor protein p53, and is thought to regulate the function of p53. Alternative splice of this gene results in 3 transcript variants encoding distinct isoforms.
保存建议：Cdc14 抗体-Cdc14 AntibodyStore at 4℃ for three months and -20℃, stable for up to one year
应用类型：WB, IHC-P, Flow
点击：Cdc14 抗体-Cdc14 Antibody查看更详细产品说明，更多应用、储存、价格、货期等信息请垂询艾美捷科技有限公司。更多ProSci公司特色试剂盒、特色抗体以及特色试剂等产品评论，请点击查看艾美捷特色产品中心。
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文献和实验throughout interphase but not in mitosis. The primary site for phosphorylation of cdc25 is at Ser216. Phosphorylated cdc25 binds to members of the 14-3-3 family of proteins which prevents its activation of cdc2. Chk1, a protein kinase involved in the DNA damage
CDC25 Dual-Specificity Protein Phosphatases: Detection and Activity Measurements
Most cyclin-dependent kinases are negatively regulated by phosphorylation of two residues, a threonine at residue 14 and a tyrosine at residue 15. These residues are dephosphorylated by the cdc25 family of dual-specificity phosphatases
【翻译】Development trends for monoclonal antibody cancer therapeutics
in the mid- to late 1980s (Refs 12–14). In addition, human mAbs derived from phage display and transgenic mice became available in the 1990s (Refs 15, 16). It should be noted that human mAbs were also made from human hybridomas, but this production method
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