TGase1 Activators belong to a class of chemical compounds that play a crucial role in the modulation of tissue transglutaminase 1 (TGase1), also known as keratinocyte transglutaminase (kTGase). TGase1 is a member of the transglutaminase enzyme family, and it is primarily expressed in the epidermal keratinocytes, which are the predominant cell type in the outermost layer of the skin, the epidermis. TGase1 is involved in a range of cellular processes, particularly in the formation of the epidermal barrier, a critical function of the skin. This enzyme catalyzes the cross-linking of proteins by forming covalent bonds between specific amino acids, a process known as protein cross-linking or transamidation. TGase1 Activators are small molecules designed to interact with TGase1, influencing its enzymatic activity and, consequently, the cross-linking of proteins within the epidermis.
The mechanism of action of TGase1 Activators typically involves binding to specific regions of the TGase1 enzyme, inducing conformational changes that may enhance or inhibit its transamidation activity. By modulating TGase1 activity, these activators impact the cross-linking of structural proteins such as keratin, filaggrin, and involucrin, which are essential for the formation of the epidermal barrier. Research into TGase1 Activators provides valuable insights into the complex regulatory mechanisms governing skin barrier function and epidermal development. Understanding how these activators interact with TGase1 contributes to our knowledge of the intricate processes involved in maintaining skin integrity and function.
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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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VE 821 | 1232410-49-9 | sc-475878 | 10 mg | ¥4062.00 | ||
VE-821是一种ATR激酶抑制剂,通过影响DNA损伤反应途径间接影响Nibrin活性。VE-821通过抑制ATR,可以改变对DNA损伤的反应,从而改变Nibrin在DNA修复中的作用。 | ||||||
ATM Kinase 抑制剂 | 587871-26-9 | sc-202963 | 2 mg | ¥1218.00 | 28 | |
ATM 激酶抑制剂 KU-55933 是应对 DNA 双链断裂的关键角色。通过抑制 ATM,这种化学物质可间接影响 Nibrin 在 DNA 修复过程中的功能。 | ||||||
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | ¥2324.00 ¥3373.00 ¥5472.00 | 10 | |
奥拉帕利是一种影响 DNA 修复机制的 PARP 抑制剂。虽然它主要针对 PARP 酶,但其对 DNA 修复的影响会对 Nibrin 介导的途径产生下游效应。 | ||||||
LY2603618 | 911222-45-2 | sc-364526 sc-364526A | 5 mg 50 mg | ¥2414.00 ¥20409.00 | ||
LY2603618 可抑制 CHK1,这是一种参与 DNA 损伤后细胞周期调控的激酶。这会间接影响 Nibrin 在 DNA 修复和细胞对 DNA 断裂反应中的功能。 | ||||||
NU 7441 | 503468-95-9 | sc-208107 | 5 mg | ¥3949.00 | 10 | |
NU7441 可抑制另一种参与 DNA 修复的激酶 DNA-PK。抑制 DNA-PK 可间接影响 Nibrin 在 DNA 损伤反应中的作用。 | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | ¥1038.00 ¥2933.00 | 42 | |
Roscovitine 可抑制细胞周期蛋白依赖性激酶(CDKs),从而影响细胞周期的调节。这会间接影响尼布林在 DNA 损伤和修复方面的活性。 | ||||||
17-AAG | 75747-14-7 | sc-200641 sc-200641A | 1 mg 5 mg | ¥745.00 ¥1726.00 | 16 | |
17-AAG 是一种 HSP90 抑制剂,可以影响各种信号通路,包括涉及 DNA 修复蛋白(如 Nibrin)的信号通路。 | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | ¥1365.00 ¥4423.00 | 148 | |
LY294002 是一种 PI3K 抑制剂,可影响多种细胞信号通路,包括与 DNA 损伤反应相关的通路,从而可能影响 Nibrin 的活性。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | ¥699.00 ¥1749.00 ¥3610.00 | 233 | |
雷帕霉素可抑制 mTOR,这是一种参与细胞生长和增殖的激酶。这可能会对涉及 Nibrin 的 DNA 损伤反应机制产生间接影响。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | ¥1467.00 ¥3046.00 | 37 | |
HDAC 抑制剂--羟肟酸(Suberoylanilide Hydroxamic Acid)会影响基因表达模式,从而可能影响 DNA 修复过程中 Nibrin 等蛋白质的表达和功能。 |