- ￥1320
- CUSABIO
- CN
- CSB-PA003877
- 2025年09月07日
- WB, IHC, ELISA; WB:1:500-1:2000, IHC:1:100-1:300, ELISA:1:10000
- Rabbit
- Human, Mouse, Rat, Monkey
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Synthesized peptide derived from Human PTEN around the non-phosphorylation site of S370.
- 亚型：
IgG
- 形态：
liquid
- 保存条件：
store at -20°C or -80°C.
- 克隆性：
Polyclonal
- 标记物：
Non-conjugated
- 适应物种：
Human, Mouse, Rat, Monkey
- 保质期：
12
- 抗原来源：
Human
- 目录编号：
N/A
- 级别：
优
- 库存：
99
- 供应商：
武汉华美生物/CUSABIO
- 宿主：
Rabbit
- 应用范围：
WB, IHC, ELISA; WB:1:500-1:2000, IHC:1:100-1:300, ELISA:1:10000
- 浓度：
参见官网
- 靶点：
PTEN
- 抗体英文名：
PTEN Antibody
- 抗体名：
PTEN Antibody
- 规格：
100ug / 50ug
PTEN|PTEN抗体|PTEN Antibody|多抗
Uniprot ID：P60484
宿主：Rabbit
反应种属：Human, Mouse, Rat, Monkey
应用：WB, IHC, ELISA; WB:1:500-1:2000, IHC:1:100-1:300, ELISA:1:10000
别名：10q23del antibody; BZS antibody; DEC antibody; GLM2 antibody; MGC11227 antibody; MHAM antibody; MMAC1 antibody; MMAC1 phosphatase and tensin homolog deleted on chromosome 10 antibody; Mutated in multiple advanced cancers 1 antibody; Phosphatase and tensin homolog antibody; Phosphatase and tensin like protein antibody; Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN antibody; Pten antibody; PTEN_HUMAN antibody; PTEN1 antibody; TEP1 antibody
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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| 武汉华美生物工程有限公司成立于2007年12月，是一家集科研、生产、销售为一体的生物高新技术企业。并形成了以CUSABIO为品牌的ELISA试剂盒、外泌体提取试剂盒、蛋白、抗体等多种优质产品，远销欧美日德等九十多个国家。 推荐您微信关注华美官方公众号，方便查询产品，同时获取生命科学更新资讯！ |
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文献和实验Genetic evidence strongly suggested that a tumor suppressor was located on chromosome 10. During the development of glioblastoma, one copy of chromosome 10 was typically lost (1 ). Cytogenetic and molecular analysis revealed partial
Measurement of PTEN Activity in vivo by Imaging Phosphorylated Akt
-dependent activation and phosphorylation of the survival kinase Akt can be used as readout for cellular PTEN activity. Here we have outlined a detailed procedure employing a phosphoserine-specific anti-Akt antibody to examine the content of phosphorylated
18 Direct Sequencing for Cowden Syndrome Gene PTEN (MMAC1) Mutations
Cowden syndrome is a rare dominantly inherited condition with predisposition to benign hamartomatous polyposis of the intestine, as well as malignant tumors of the breast and thyroid, and possibly some other cancer types. Other features include
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