- ¥1 - 3980
- PEPROTECH
- 中国/美国
- xy-644Hu01
- 2025年12月23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：
-20℃
- 保质期：
12个月
- 英文名：
Recombinant Phosphodiesterase 4D, cAMP Specific (PDE4D)
- 库存：
1000
- 供应商：
上海信裕
| Organism species | Homo sapiens (Human) |
| Product No. | xy644Hu01 |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | > 90% |
| UOM | 50ug |
| Predicted Molecular Mass | 56.1kDa |
| Concentration | n/a |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Formulation | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
Stability Test: The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37oC for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition.
Protein bands: 10kDa, 14kDa, 18kDa, 22kDa, 26kDa, 33kDa, 44kDa and 70kDa.
Double intensity bands: The 26kDa, 18kDa, 10kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy.
磷酸二酯酶4D(PDE4D)重组蛋白Ready-to-use: No need to heat, dilute or add reducing agents before use.
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文献和实验打破传统认知，降糖不仅依赖胰岛素！科学家发现，这种来自脂肪的激素也可以调节血糖……
在体内具有调节脂肪分解的能力，因此他们接下来也探索了 PDE4D 在 FGF1 代谢作用中的作用。他们惊喜地发现，在稳态和 ISO 刺激下，PDE4DKO 小鼠的脂肪分解显著较高，但其对 FGF1 的处理则不敏感。更重要的是，FGF1 并不能降低这些高脂肪喂养 PDE4DKO 小鼠的血糖。这些数据表明，脂肪 PDE4D 是外源性 FGF1 降糖作用所必需的。 图片来源：Cell Metabolism FGF1 诱导 PDE4D 调控位点的磷酸化 磷酸二酯酶的活性受多种磷酸化事件的调控
centrifugations to calculate the mass of a protein independently of its shape or hydration. It has been shown previously that PDE4D3, a representative of the long PDE4 splice forms, behaves as a dimer, whereas PDE4D2, a prototype of the short PDE4 splice forms
Crystallization of Cyclic Nucleotide Phosphodiesterases
inhibitors, but their availability is limited by the speed of crystallization. We describe crystallization of the catalytic domains of the unligated PDE4B2B, rolipram-bound PDE4D2, and 3-isobutyl-1-methylxanthine-bound PDE5A1 using the methods of vapor
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