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5-Ph-IAA-AM Sale

目录号 : GC64397

5-Ph-IAA-AM 是一种可渗透卵壳的 5-Ph-IAA 类似物。5-Ph-IAA-AM 增强了虫卵的蛋白降解。 5-Ph-IAA-AM 可用于揭示秀丽隐杆线虫蛋白质的作用,特别是那些通过时间控制的参与胚胎发生和发育的蛋白质降解。

5-Ph-IAA-AM Chemical Structure

规格 价格 库存 购买数量
5 mg
¥2,070.00
现货
10 mg
¥3,240.00
现货
25 mg
¥6,480.00
现货
50 mg
¥10,350.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

5-Ph-IAA-AM is an eggshell-permeable 5-Ph-IAA analog. 5-Ph-IAA-AM affords an enhanced protein degradation in laid embryos. 5-Ph-IAA-AM can be used to disclosure the roles of proteins in C. elegans, in particular those that are involved in embryogenesis and development, through temporally controlled protein degradation[1].

[1]. Negishi T, et al. The auxin-inducible degron 2 (AID2) system enables controlled protein knockdown during embryogenesis and development in Caenorhabditis elegans. Genetics. 2022 Feb 4;220(2):iyab218.

Chemical Properties

Cas No. SDF Download SDF
分子式 C19H17NO4 分子量 323.34
溶解度 DMSO : 100 mg/mL (309.27 mM; Need ultrasonic) 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 3.0927 mL 15.4636 mL 30.9272 mL
5 mM 0.6185 mL 3.0927 mL 6.1854 mL
10 mM 0.3093 mL 1.5464 mL 3.0927 mL
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Research Update

The auxin-inducible degron 2 (AID2) system enables controlled protein knockdown during embryogenesis and development in Caenorhabditis elegans

Genetics 2022 Feb 4;220(2):iyab218.PMID:34865044DOI:PMC9208642

Targeted protein degradation using the auxin-inducible degron (AID) system is garnering attention in the research field of Caenorhabditis elegans, because of the rapid and efficient target depletion it affords, which can be controlled by treating the animals with the phytohormone auxin. However, the current AID system has drawbacks, i.e., leaky degradation in the absence of auxin and the requirement for high auxin doses. Furthermore, it is challenging to deplete degron-fused proteins in embryos because of their eggshell, which blocks auxin permeability. Here, we apply an improved AID2 system utilizing AtTIR1(F79G) and 5-phenyl-indole-3-acetic acid (5-Ph-IAA) to C. elegans and demonstrated that it confers better degradation control vs the previous system by suppressing leaky degradation and inducing sharp degradation using 1,300-fold lower 5-Ph-IAA doses. We successfully degraded the endogenous histone H2A.Z protein fused to an mAID degron and disclosed its requirement in larval growth and reproduction, regardless of the presence of maternally inherited H2A.Z molecules. Moreover, we developed an eggshell-permeable 5-Ph-IAA analog, 5-Ph-IAA-AM, that affords an enhanced degradation in laid embryos. Our improved system will contribute to the disclosure of the roles of proteins in C. elegans, in particular those that are involved in embryogenesis and development, through temporally controlled protein degradation.