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  • 化合物 SCR7|T3340|TargetMol

化合物 SCR7|T3340|TargetMol

SCR7
1533426-72-0
560 1mg 起订
1900 5mg 起订
3220 10mg 起订
上海 更新日期:2024-09-29

TargetMol中国(陶术生物)

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邮箱:marketing@tsbiochem.com

产品详情:

中文名称:
化合物 SCR7
英文名称:
SCR7
CAS号:
1533426-72-0
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
产品类别:
抑制剂
货号:
T3340

Product Introduction

Bioactivity

NameSCR7
DescriptionSCR7, a specific DNA Ligase IV inhibitor, blocks nonhomologous end-joining (NHEJ).
Cell ResearchSCR7 is dissolved in DMSO and stored, and then diluted with appropriate medium before use[3]. Wild-type, AAVS1TLR HEK293 and mouse NIH3T3 cells are maintained in DMEM supplied with 15% FBS, cells are passaged three times per week. The mouse Burkitt lymphoma cell line, generated from a Burkitt-like mouse lymphoma is maintained in DMEM supplied with 15% FBS, 2 mM HEPES, 2 mM sodium pyruvate, 2 mM L-glutamine, and 1× NAA, beta-mercaptoethanol and passaged four times per week. For puromycin selection, mCherry+ cells are sorted, seeded at 103 cells/well and selected with 3 mg/mL of Puromycin for 2 weeks. Then colonies are counted and single cells are sorted. The SCR7 inhibitor is purchased, 12 h after transfection these cells are maintained in complete medium supplied with 1 mM SCR7 inhibitor until analysis. At SCR7 concentrations of 60 mM and 10 mM, A reduction of transfection efficiency and of cell viability is observed[3].
Kinase AssayComplementation of SCR7 Inhibition with Puri?ed Ligase IV: Complementation experiment is carried out by adding increasing concentrations of puri?ed Ligase IV/XRCC4 complex (30, 60, and 120 fmol) along with the oligomeric DNA substrates (5' compatible and 5'-5' noncompatible ends) to the SCR7-treatedextracts. Reactions are incubated for 2 h at 25℃. The reaction products are then resolved on 8% denaturing PAGE. The gel is dried and exposed and the signal is detected with a PhosphorImager and analyzed with Multi Gauge (V3.0) software.
In vitro在负荷Dalton's淋巴瘤的Swiss albino小鼠模型中,腹腔注射SCR7(20 mg/kg)不能够消退肿瘤.在BALB/c小鼠体内,腹腔注射SCR7(20 mg/kg)能够增强辐射,依托泊苷和3-氨基苯甲酰胺对于Dalton's淋巴瘤细胞的衍生瘤的细胞毒性作用.
In vivo在MCF7细胞(IC50=40 μM),A549细胞(IC50=34 μM),HeLa细胞(IC50=44 μM),T47D细胞(IC50=8.5 μM),A2780细胞(IC50=120 μM),HT1080细胞(IC50=10 μM),和Nalm6细胞(IC50=50 μM)中,SCR7能够显著抑制细胞增殖。
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 45 mg/mL (134.57 mM)
Keywordsgene | end-joining | nonhomologous | SCR 7 | DNA/RNA Synthesis | Caspase 9 | phosphorylation | SCR7 | CRISPR/Cas9 | Caspase 3 | ligase-IV | SCR-7 | inhibit | replacement | Apoptosis | Inhibitor | DNA | anticancer
Inhibitors RelatedGuanidine hydrochloride | Metronidazole | 5-Fluorouracil | Stavudine | Tributyrin | Dextran sulfate sodium salt (MW 4500-5500) | Myricetin | Sorafenib | L-Ascorbic acid | Acetylcysteine | Thymidine | Sodium 4-phenylbutyrate
SCR7|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

成立日期 (12年)
注册资本 566.265100万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,工厂,试剂,定制,服务
主营行业 天然产物,生化试剂,分子生物学,分子砌块,生物技术服务

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