1700009P17Rik activators are a specialized class of chemical compounds that enhance the activity of the protein encoded by the 1700009P17Rik gene. This gene, like many others identified through genomic sequencing, is not extensively characterized, but it is believed to play a role in various cellular processes based on its expression profile and potential protein interactions. Activators of 1700009P17Rik are designed to increase the activity or expression of the protein, thereby amplifying its functional impact within the cell. These activators may work by binding directly to the protein, inducing conformational changes that enhance its function, or by influencing the gene's expression, leading to an upregulation of the protein at the transcriptional or translational level.
The mechanisms through which 1700009P17Rik activators operate can vary depending on the nature of the protein and its role within the cell. Some activators may stabilize the active form of the protein, preventing its degradation and prolonging its functional presence within the cell. Others may increase the protein's affinity for its substrates or interaction partners, thereby boosting its activity in specific signaling pathways or cellular processes. The activation of 1700009P17Rik can lead to significant changes in the cellular environment, potentially influencing pathways related to gene expression, signal transduction, or metabolic regulation. Studying these activators provides critical insights into the function of the 1700009P17Rik protein and its broader role in cellular physiology. By modulating this protein's activity, researchers can uncover new aspects of cellular regulation and gain a deeper understanding of how specific genes contribute to the maintenance of cellular homeostasis and the dynamic responses of cells to their environment.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Adenosine 3′,5′-cyclic monophosphate | 60-92-4 | sc-217584 sc-217584A sc-217584B sc-217584C sc-217584D sc-217584E | 100 mg 250 mg 5 g 10 g 25 g 50 g | ¥1286.00 ¥1974.00 ¥2933.00 ¥4084.00 ¥6961.00 ¥12715.00 | ||
db-cAMP 是一种具有细胞渗透性的 cAMP 类似物,可以激活 PKA。通过激活 PKA,db-cAMP 可以磷酸化和激活涉及 Flattop 的通路中的蛋白质,从而增强其活性。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | ¥301.00 ¥1128.00 | 257 | |
JNK 抑制剂,可影响应激反应和细胞凋亡途径。 | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | ¥745.00 ¥2471.00 ¥4705.00 | 97 | |
PI3K 抑制剂可影响各种信号通路。 | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | ¥2414.00 | ||
氯化锂抑制糖原合酶激酶-3(GSK-3)。抑制GSK-3可激活Wnt信号通路,而Wnt信号通路可能与Flattop通路交叉,从而增强Flattop的活性。 | ||||||
1,2-Dioctanoyl-sn-glycerol | 60514-48-9 | sc-202397 sc-202397A | 10 mg 50 mg | ¥519.00 ¥2809.00 | 2 | |
DiC8是二酰基甘油(DAG)的合成类似物,也是PKC的激活剂。DiC8激活PKC后,Flattop参与其中的信号传导通路中的蛋白质就会发生磷酸化,从而增强其活性。 | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | ¥1489.00 ¥12004.00 | 115 | |
蛋白酶体抑制剂,可影响蛋白质降解过程。 | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | ¥654.00 ¥1918.00 | 15 | |
钙通道阻滞剂,可影响钙信号传导。 | ||||||
Ouabain-d3 (Major) | sc-478417 | 1 mg | ¥5709.00 | |||
欧贝因是Na⁺/K⁺-ATPase泵的抑制剂,可导致细胞内钠和钙水平升高。这种离子浓度的变化可能会激活信号通路,间接增强 Flattop 的活性。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | ¥1467.00 ¥3046.00 | 37 | |
HDAC 抑制剂可影响基因表达过程。 |