- ￥6200 - 9700
- GeneTex
- 美国
- GTX17672-pro
- 2025年07月09日
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 保存条件：
Store as concentrated solution. Aliquot and store at -20ºC or below. Avoid freeze-thaw cycles.
- 保质期：
12 months from the shipping date of the product.
- 英文名：
Human Tau441 (2N4R) protein, mutant P301S (monomer)
- 库存：
Available
- 供应商：
GeneTex
- 规格：
200 μg/100 μg
| 规格： | 200 μg | 产品价格： | ￥9700.0 |
|---|---|---|---|
| 规格： | 100 μg | 产品价格： | ￥6200.0 |
Thioflavin T is a fluorescent dye that binds to beta sheet-rich structures, such as those in tau fibrils. Upon binding, the emission spectrum of the dye experiences a red-shift and increased fluorescence intensity. Thioflavin T emission curves show increased fluorescence (correlated to tau aggregation) over time in tau monomers (GTX17672-pro). A greater increase in fluorescence is seen when 50 uM monomer (GTX17672-pro) is combined with 10 nM PFFs (GTX17674-pro or GTX17675-pro), as the fibrils seed the formation of new fibrils from the pool of monomers. Thioflavin T ex = 450 nm, em = 485 nm.
SDS-PAGE of ~67 kDa Human Tau441 (2N4R) protein, mutant P301S (monomer) (GTX17672-pro).
Lane 1: MW ladder. Lane 2: Human Tau441 (2N4R) protein, mutant P301S (monomer) (GTX17672-pro).
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- 内容
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文献和实验Cell-Based Assays for Regulators of Tau Biology
, which may ultimately lead to translational outcomes for AD. In particular, the intracellular microtubule-associated protein tau that accumulates in AD is found in normal cells. Manipulating these cells may allow us to address basic questions about tau biology
DamIP: Using Mutant DNA Adenine Methyltransferase to Study DNA‐Protein Interactions In Vivo
for studying DNA?protein interaction in vivo. A mutant form of DNA adenine methyltransferase (DamK9A) from E. coli is fused to the protein of interest and expressed. The fusion protein will bind to target binding sites and introduce N 6 ?adenine methylation
Generation and Characterization of p53 Mutant Mice
of the p53 knock-out mouse demonstrated the protein’s dispensability during embryogenesis, while highlighting its essential role in controlling tumor formation. A variety of p53 mutant models have emerged since the original p53 knock-out mouse
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