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RS-1 {[allProObj[0].p_purity_real_show]}

货号:A122463

RS-1 increases the DNA binding activity of RAD51. It can also act as an enhancer of homology-directed repair and CRISPR/Cas9 mediated knock-in efficiency.

RS-1 化学结构 CAS号:312756-74-4
RS-1 化学结构
CAS号:312756-74-4
RS-1 3D分子结构
CAS号:312756-74-4
RS-1 化学结构 CAS号:312756-74-4
RS-1 3D分子结构 CAS号:312756-74-4
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RS-1 纯度/质量文件 产品仅供科研

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RS-1 生物活性

描述 RAD51 filament formation is a key step in homologous recombination repair. RS-1 is a small molecule that enhances RAD51 binding and filament stability. RS-1 at a concentration of 0, 1–25μM stimulated strand assimilation activity of RAD51. RS-1 at 7.5μM promoted resistance of human cells to cross-linking chemotherapy[3]. Treatment of embryos with 7.5μM of RS-1 resulted in a significantly higher knock-in rate compared with the control group (26.1% vs. 4.4%). RS-1 at a dose of 7.5 and 15 μM also improved TALEN- and Cas9-mediated knock-in efficiency in rabbit embryos[4].

RS-1 细胞实验

Cell Line
Concentration Treated Time Description References
Porcine embryo cells 7.5 µM and 15 µM 20 hours and 144 hours To evaluate the effects of RS-1 on porcine embryo development in vitro. Results showed that transient exposure to 7.5 μM RS-1 did not affect embryo development, while 15 μM RS-1 reduced cleavage rates. Long-term exposure to 7.5 μM RS-1 decreased blastocyst formation rates. Reprod Toxicol. 2021 Oct;105:44-52
Mouse SCNT embryos 10 µM 22 hours RS-1 treatment significantly improved the blastocyst formation rate and enhanced embryo morphology and development. Cell Prolif. 2021 Jul;54(7):e13059
Normal neonatal human dermal fibroblasts 1–7.5 µM 24 hours Assess RS-1 effect on cisplatin resistance, RS-1 promotes dose-dependent resistance Proc Natl Acad Sci U S A. 2008 Oct 14;105(41):15848-53
Tobacco leaf 25 µM 30 minutes To assess the effect of RS-1 on tobacco leaves for subsequent Agrobacterium-mediated transformation experiments Front Genome Ed. 2020 Nov 25;2:604289
Rice callus 25 µM 30 minutes To evaluate the cytotoxicity of RS-1 on rice callus, showing no significant effect on growth at 25 µM RS-1 Front Genome Ed. 2020 Nov 25;2:604289
HEK293T cells 10 µM 42 hours Stimulation of RAD51 significantly increased the knockin efficiency of the mito-Cas9 system Innovation (Camb). 2022 Sep 27;3(6):100329
MRC-5 normal primary human fibroblasts 60 µM 6 hours RS-1 treatment did not significantly induce RAD51 nuclear protein foci formation Cancer Res. 2014 Jul 1;74(13):3546-55
PC3 prostate cancer cells 60 µM 6 hours RS-1 treatment induced the formation of RAD51 nuclear protein foci, accompanied by cell death Cancer Res. 2014 Jul 1;74(13):3546-55

RS-1 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice SCNT cloned embryos Added to in vitro culture medium 10 µM Single treatment, lasting 22 hours RS-1 treatment significantly improved the developmental efficiency of SCNT cloned embryos and the birth rate of cloned mice. Cell Prolif. 2021 Jul;54(7):e13059
Athymic nude mice PC3 xenograft tumor model Intraperitoneal injection 110 mg/kg Once daily for 5 days RS-1 treatment significantly inhibited tumor growth, with 43% of tumors completely disappearing Cancer Res. 2014 Jul 1;74(13):3546-55
Rice (Oryza sativa L. cv. Nipponbare) Rice callus Medium treatment 25 µM 30 minutes treatment, followed by culture in medium containing 25 µM RS-1 for 2 weeks To evaluate the effect of RS-1 on CRISPR/Cas9-mediated gene targeting frequency, showing a slight but consistent improvement in gene targeting frequency with RS-1 treatment Front Genome Ed. 2020 Nov 25;2:604289
Pig In vitro-produced embryo transfer model In vitro culture 7.5 μM 20 hours To evaluate the effects of RS-1 on porcine embryo development in vivo. Results showed that transient exposure to 7.5 μM RS-1 was compatible with in vivo development, successfully producing healthy piglets. Reprod Toxicol. 2021 Oct;105:44-52

RS-1 参考文献

[1]Song J, Yang D, et al. RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency. Nat Commun. 2016 Jan 28;7:10548.

[2]Mason JM, Logan HL, et al. The RAD51-stimulatory compound RS-1 can exploit the RAD51 overexpression that exists in cancer cells and tumors. Cancer Res. 2014;74(13):3546-55.

[3]Jayathilaka K, Sheridan SD, Bold TD, et al. A chemical compound that stimulates the human homologous recombination protein RAD51. Proc Natl Acad Sci U S A. 2008;105(41):15848-15853. doi:10.1073/pnas.0808046105

[4]Song J, Yang D, Xu J, Zhu T, Chen YE, Zhang J. RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency. Nat Commun. 2016;7:10548. Published 2016 Jan 28. doi:10.1038/ncomms10548

RS-1 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.91mL

0.38mL

0.19mL

9.54mL

1.91mL

0.95mL

19.08mL

3.82mL

1.91mL

RS-1 技术信息

CAS号312756-74-4
分子式C20H16Br2N2O3S
分子量 524.23
SMILES Code O=C(NC1=CC=C(Br)C=C1)C2=CC=C(Br)C(S(=O)(NCC3=CC=CC=C3)=O)=C2
MDL No. MFCD00348720
别名
运输蓝冰
InChI Key SWKAVEUTKGKHSR-UHFFFAOYSA-N
Pubchem ID 1039737
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, room temperature

溶解方案

DMSO: 105 mg/mL(200.3 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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