1700030K09Rik Activators encompass a diverse array of chemical compounds that indirectly enhance the functional activity of 1700030K09Rik through various signaling pathways. Forskolin and IBMX both work to increase intracellular levels of cAMP, leading to the activation of PKA, which is known to phosphorylate an array of proteins, potentially including 1700030K09Rik, to enhance its cellular functions. Similarly, the activation of PKC by PMA could lead to phosphorylation events that activate 1700030K09Rik. Ionomycin and A23187, both calcium ionophores, elevate intracellular calcium levels, a critical secondary messenger that activates calcium-dependent kinases capable of enhancing the activity of proteins such as 1700030K09Rik. The kinase inhibitory actions of Epigallocatechin Gallate (EGCG) and the phosphoinositide 3-kinase (PI3K) inhibitor LY294002, as well as U0126 and SB203580, which target MEK and p38 MAPK respectively, could indirectly lead to the activation of 1700030K09Rik by shifting the equilibrium of cellular signaling.
Moreover, Sphingosine-1-phosphate signals through its kinase to potentiate cellular pathways, possibly leading to increased activity of 1700030K09Rik. Genistein's inhibition of tyrosine kinases might reduce competitive signaling pathways, thereby enhancing the functional role of 1700030K09Rik. Lastly, Staurosporine, while a broad-spectrum kinase inhibitor, has the potential to selectively activate 1700030K09Rik by alleviating inhibitory kinases that might otherwise suppress its activity. Collectively, these chemicals provide a multifaceted approach to enhancing the activation of 1700030K09Rik, each through a unique mechanism that converges on the modulation of specific signaling pathways within the cell, emphasizing the complex regulatory nature of protein activity.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
作为强效抗氧化剂,表没食子儿茶素没食子酸酯可以影响氧化还原敏感的信号通路。这可能会改变信号环境,通过改变氧化状态间接激活1700030K09Rik,而氧化状态可以调节多种蛋白质的功能。 | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA 是蛋白激酶 C (PKC) 的激活剂。PKC 可使调节 1700030K09Rik 活性的中间产物磷酸化,从而增强其功能活性。 | ||||||
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $76.00 $265.00 | 80 | |
离子霉素是一种钙离子载体,可增加细胞内钙离子浓度,从而激活钙依赖性蛋白激酶,后者能够磷酸化1700030K09Rik,从而增强其活性。 | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002是一种PI3K抑制剂,可以改变AKT信号传导。通过调节该通路,其他补偿性通路可能会上调,从而通过反馈机制激活1700030K09Rik。 | ||||||
D-erythro-Sphingosine-1-phosphate | 26993-30-6 | sc-201383 sc-201383D sc-201383A sc-201383B sc-201383C | 1 mg 2 mg 5 mg 10 mg 25 mg | $162.00 $316.00 $559.00 $889.00 $1693.00 | 7 | |
这种脂质信号分子可以激活鞘氨醇-1-磷酸受体,后者是信号级联的一部分,可通过影响细胞的脂质信号环境来激活1700030K09Rik。 | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $54.00 $128.00 $199.00 $311.00 | 23 | |
A23187 是一种钙离子拮抗剂,它能提高细胞内的钙含量,从而可能激活钙依赖性信号通路,使 1700030K09Rik 参与其中,增强其活性。 | ||||||
Amiloride • HCl | 2016-88-8 | sc-3578 sc-3578A | 25 mg 100 mg | $22.00 $56.00 | 6 | |
氨氯地平抑制钠离子通道和Na+/H+交换。这种离子平衡的调节可通过改变细胞内稳态和依赖离子通量的信号通路间接激活1700030K09Rik。 | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580是p38 MAPK的特异性抑制剂。抑制p38 MAPK可激活包括1700030K09Rik在内的其他信号通路,从而间接增强其活性。 | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $47.00 | ||
氯化锌可以作为锌离子载体,增加细胞内锌的含量,从而调节包括可能与1700030K09Rik结合的信号通路,使其激活。 |