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- 2026年04月28日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
蛋白表达区间:Lys44-Ala750
- 保质期：
See instructions
- 英文名：
标签:N-6His
- 库存：
表达系统:Human Cells
- 供应商：
上海经科化学科技有限公司
- 规格：
10ug/50ug/500ug/1mg
| 规格： | 10ug | 产品价格： | ￥1200.0 |
|---|---|---|---|
| 规格： | 50ug | 产品价格： | ￥3520.0 |
| 规格： | 500ug | 产品价格： | ￥13440.0 |
| 规格： | 1mg | 产品价格： | ￥19200.0 |
- The product is shipped on dry ice/polar packs.
- Upon receipt, store it immediately at the temperature listed below.
- Store at ≤-70°C, stable for 6 months after receipt.
- Store at ≤-70°C, stable for 3 months under sterile conditions after opening.
- Please minimize freeze-thaw cycles.
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文献和实验Glutamate carboxypeptidase 2, also known as FOLH1, PSMA, belongs to the M28B subfamily and the peptidase M28 family. It is highly expressed in prostate epithelium and can be detected in urinary bladder, kidney, testis, ovary, fallopian tube, breast, adrenal gland, liver, esophagus, stomach, small intestine, colon and brain (at protein level). PSMA is used as a diagnostic and prognostic indicator of prostate cancer, and as a possible marker for various neurological disorders such as schizophrenia, Alzheimer disease and Huntington disease. It has both folate hydrolase and N-acetylated-alpha-linked-acidic dipeptidase (NAALADase) activity and has a preference for tri-alpha-glutamate peptides. PSMA involves in prostate tumor progression and also exhibits a dipeptidyl-peptidase IV type activity. In vitro, PSMA cleaves Gly-Pro-AMC. PSMA is stable at pH greater than 6.5.
Deorphanization of Human Olfactory Receptors by Luciferase and Ca-Imaging Methods
to induce intracellular calcium elevation. Two independent tests, Ca-imaging and CRE-Luciferase assays, have been used in the deorphanization of human ORs and in the analysis of their responses to chemical compounds
Culturing Human Embryonic Stem Cells in Feeder-Free Conditions
, Department of Obstetrics and Gynecology, Stanford University, Palo Alto, CA 94304-5542, USA 1 Corresponding author (sohyun@stanford.edu ) INTRODUCTION Human embryonic stem cells (hESCs) have the potential to differentiate
Measurement of Ca2+-ATPase Activity (in PMCA and SERCA1)
and a purified enzyme, best suited for studies of Ca2+ -ATPase activity are described. The two selected membranes are the human red blood cell (RBC) ghosts, a representative of plasma membranes (PM), and the rabbit skeletal muscle SR, an intracellular membrane
技术资料
