- ￥2860
- LSM BIO
- 进口
- PAab10258
- 2025年07月07日
- ELISA, WB, IHC
- E. coli - derived recombinant protein
- Human, Rat
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 免疫原：
protein tyrosine phosphatase, non-receptor type 1
- 亚型：
IgG
- 形态：
liquid
- 保存条件：
负20摄氏度
- 克隆性：
polyclonal
- 标记物：
Non-conjugated
- 适应物种：
Human, Rat
- 保质期：
6个月
- 抗原来源：
Rabbit
- 目录编号：
P04085
- 级别：
纯化级别
- 库存：
50
- 供应商：
LSM bio
- 宿主：
E. coli - derived recombinant protein
- 应用范围：
ELISA, WB, IHC
- 浓度：
≥95% as determined by SDS-PAGE
- 靶点：
protein tyrosine phosphatase, non-receptor type 1
- 抗体英文名：
PTEN antibody
- 抗体名：
PTEN antibody|PTEN 抗体
- 规格：
100μl
PTEN antibody
Product Name PTEN antibody
Catalog No PAab10258
Packing 100ul
Form liquid
Alternative Name MMAC1, TEP1
Purification Immunogen affinity purified
Purity 95% as determined by SDS-PAGE
Host Rabbit
Isotype IgG
Storage PBS with 0.02% sodium azide and 50% glycerol pH 7.3 , -20Centigrade for 24 months (Avoid repeated freeze / thaw cycles.)
Background/ FUNCTION
Immunogen phosphatase and tensin homolog
Specificity Human, Rat
Tested Application ELISA, WB
Recommended dilution WB: 1:500 - 1:2000
IHC use
WB use
Hela cells were subjected to SDS PAGE followed by western blot with PAab10258( PTEN Antibody) at dilution of 1:1000
Protein Information
Gene ID
Uniprot ID P60484
Calculated MW 55 kDa
Research Area Signal Transduction, Metabolism, Cardiovascular, Immunology, Cancer, Neuroscience, Stem Cells, Cell Division and Proliferation
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- 作者
- 内容
- 询问日期
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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