Anhydrotetracycline (hydrochloride)
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 10mg | ¥1360.00 | 现货 | |
| 25mg | ¥2455.00 | 现货 | |
| 50mg | ¥3190.00 | 现货 | |
| 100mg | ¥3904.00 | 现货 | |
| 250mg | ¥4470.00 | 现货 | |
| 500mg | ¥6832.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Anhydrotetracycline (hydrochloride) (ATC) is a powerful effector for the tetracycline repressor (TetR) and reverse tetracycline repressor (revTetR) systems [1].
Tetracycline repressor (TetR) is an effector-regulated DNA-binding protein that binds tightly to its palindromic tetO operator DNA in the absence of effector, thereby blocking the transcription of any downstream genes. Binding of tetracycline (TC) or anhydrote-tracycline (ATC) to TetR causes the repressor to dissociate from the DNA and gene transcription can occur. Contrary to TetR, reverse tetracycline repressor (revTetR) mutant binds tetO only in the presence of ATC [2][3].
Anhydrotetracycline (hydrochloride) is a powerful effector for TetR and revTetR systems. Anhydrotetracycline (ATC) bound TetR with a 500-fold higher affinity and represented the most efficient inducer [2]. ATC bound the Tet repressor 35-fold more potent than Tet [4]. However, ATC acted as a corepressor in revTetR variant. In β-galactosidase (β-gal) assays, TetR inhibitedβ-gal expression to nearly 1%, while ~100% expression was accomplished in the presence of 0.4 μM ATC. RevTetR produced almost 100%β-gal activity in the absence of ATC, while the presence of 0.4 μM ATC resulted in a 5-fold decrease ofβ-gal activity [2].
References:
[1]. Gossen M, Bujard H. Anhydrotetracycline, a novel effector for tetracycline controlled gene expression systems in eukaryotic cells. Nucleic Acids Res. 1993 Sep 11;21(18):4411-2.
[2]. Kamionka A, Bogdanska-Urbaniak J, Scholz O, et al. Two mutations in the tetracycline repressor change the inducer anhydrotetracycline to a corepressor. Nucleic Acids Res. 2004 Feb 4;32(2):842-7.
[3]. Resch M, Striegl H, Henssler EM, et al. A protein functional leap: how a single mutation reverses the function of the transcription regulator TetR. Nucleic Acids Res. 2008 Aug;36(13):4390-401.
[4]. Degenkolb J, Takahashi M, Ellestad GA, et al. Structural requirements of tetracycline-Tet repressor interaction: determination of equilibrium binding constants for tetracycline analogs with the Tet repressor. Antimicrob Agents Chemother. 1991 Aug;35(8):1591-5.
产品性质
| 物理外观 | Solid |
| CAS号 | 13803-65-1 |
| 分子式 | C22H22N2O7·HCl |
| 分子量 | 462.9 |
| 小分子别名 | Anhydrotetracycline hydrochloride |
| 化学名称 | 4-(dimethylamino)-1,4S,4aS,5,12,12aS-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-monohydrochloride-2-naphthacenecarboxamide |
| 溶解度 | ≥12.5 mg/mL in H2O; ≥15.43 mg/mL in EtOH with gentle warming; ≥2.42 mg/mL in DMSO with ultrasonic |
| SMILES | Cc(c1c2c(O)ccc1)c(C[C@@H]([C@@H](C(OCl)=C(C(N)=O)C1=O)N(C)C)[C@@]1(C1=O)O)c1c2O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 盐酸金霉素是一种四环素生物合成前体,是一种强效的竞争性广谱四环素破坏酶抑制剂。盐酸金霉素是真核细胞中四环素控制基因表达系统的一种效应物。 |



沪公网安备 31011002003500