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顺铂

CAS:No.15663-27-1

英文名称:Cisplatin

分子式:Cl2H6N2Pt

分子量:300.05

储存条件:Powder: 2-8℃,2 years

纯度:HPLC≥98%

顺铂
满3999赠露营车
货号:
IC0440
品牌:
Solarbio
SKU 北京总部 北京海淀 武汉 广州
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使用本产品的应用案例(仅供参考):

In Vivo

Mice(Four- to 6-week-old male BALB/C nude mice5 mg/kg cisplatinintraperitoneally administeredevery week for 2 weeks

Four- to 6-week-old male BALB/C nude mice were subcutaneously injected with 1 × 106 cells near the extremities of four limbs. When the mice developed palpable tumors, the mice were intraperitoneally administered with cisplatin (5 mg/kg; Solarbio Company) every week for 2 weeks. The size of the tumors was measured once every 3 days, six times in a row.  All animals were sacrificed 25 days after inoculation, and the tumors were collected.The tumor tissues were photographed, and immunohistochemistry was performed.

来源文献:Gong L, Xiao M, He D, Hu Y, Zhu Y, Xiang L, Bao Y, Liu X, Zeng Q, Liu J, Zhou M, Zhou Y, Cheng Y, Zhang Y, Deng L, Zhu R, Lan H, Cao K. WDHD1 Leads to Cisplatin Resistance by Promoting MAPRE2 Ubiquitination in Lung Adenocarcinoma.  Front Oncol. 2020 Apr 24;10:461.  doi: 10.3389/fonc.2020.00461.  PMID: 32426268;  PMCID: PMC7212426.



Mice (Heterozygous DDX39A knockout mice (C57BL/6N), after overnight incubation, the cells were exposed to various concentrations of cisplatin for a duration of 48 hours)

Cisplatin-resistant HCT116 and SKOV3 cells, denoted HCT116/DDP and SKOV3/DDP, respectively, were generated by subjecting the corresponding parental cells to prolonged treatment with incrementally increasing concentrations of cisplatin.

To assess cellular drug sensitivity, a CCK-8 assay was used. Initially, cells were seeded into 96-well plates at a density of 4000 cells per well. After overnight incubation, the cells were exposed to various concentrations of cisplatin for a duration of 48 hours. Subsequently, 10 mLof CCK-8 solution was added to each well, followed by a 2-hour incubation.

来源文献:Xu Z, Nie C, Liao J, Ma Y, Zhou XA, Li X, Li S, Lin H, Luo Y, Cheng K, Mao Z, Zhang L, Pan Y, Chen Y, Wang W, Wang J. DDX39A resolves replication fork-associated RNA-DNA hybrids to balance fork protection and cleavage for genomic stability maintenance. Mol Cell. 2024 Dec 13:S1097-2765(24)00954-7. doi: 10.1016/j.molcel.2024.11.029. Epub ahead of print. PMID: 39706185.


In Vitro

CellHCT116 and SKOV3 cellsvarious concentrations of cisplatin for a duration of 48 hours

To assess cellular drug sensitivity, a CCK-8 assay was used. Initially, cells were seeded into 96-well plates at a density of 4000 cells per well. After overnight incubation, the cells were exposed to various concentrations of cisplatin for a duration of 48 hours. Subsequently, 10 mLof CCK-8 solution was added to each well, followed by a 2-hour incubation. The absorbance was measured using a microplate reader at a wavelength of 450 nm. Semilogarithmic dose-response curves for cisplatin were generated using GraphPad Prism.

文献来源:Xu Z, Nie C, Liao J, Ma Y, Zhou XA, Li X, Li S, Lin H, Luo Y, Cheng K, Mao Z, Zhang L, Pan Y, Chen Y, Wang W, Wang J. DDX39A resolves replication fork-associated RNA-DNA hybrids to balance fork protection and cleavage for genomic stability maintenance. Mol Cell. 2025 Feb 6;85(3):490-505.e11. doi: 10.1016/j.molcel.2024.11.029. Epub 2024 Dec 19. PMID: 39706185.


CellPlatinum-sensitive humanovarian papillary serous adenocarcinoma cell line OV-90 (ATCC#CRL11732)10, 20, 40, 80, 100, and 120mM to generate chemoresistant OV-90/DDP cell lines

Cells were subjected to treatment with escalating concentrations of cisplatin (DDP, IC0440,Beijing Solarbio Science and Technology Co.), specically 10, 20, 40,80, 100, and 120mM to generate chemoresistant OV-90/DDP cell lines. Cisplatin at a concentration of 10 mM was introduced when the cells reached the exponential phase, with subsequent concentrations administered at the same phase until a final concentration of 120 mM was achieved. The culture conditions of the cell lines were preserved in accordance with those of the original OV-90 cell line during the entire culture period. Cells from each concentration phase were cultured with platinum drugs for a minimum of two weeks, with medium changes occurring every two days. Cisplatin-resistantsubclones were generated by intermittently exposing cells to 2 mM cisplatin while maintaining aconcentration of 100 mM to sustain chemoresistant clones. The concentration indicates the threshold that cells can endure without compromising reproductive viability. The resistant cell line OV-90/DDP was established after 12 months of induction. The cell line tested negative for mycoplasma contamination.

来源文献:Ren F, Pang X, Jin F, Luan N, Guo H, Zhu L. Integration of scRNA-seq and bulk RNA-seq to reveal the association and potential molecular mechanisms of metabolic reprogramming regulated by lactylation and chemotherapy resistance in ovarian cancer. Front Immunol. 2025 Feb 28;16:1513806. doi: 10.3389/fimmu.2025.1513806. PMID: 40093000; PMCID: PMC11907005.


备注:
以上数据均来自公开文献, Solarbio暂未进行独立验证, 仅供参考。
These protocols are for reference only. Solarbio does not independently validate these methods.

实验图
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Liu H, et al. Breast Cancer Res. 2023 Apr 17;25(1):43.
Pan Y, et al. Microsyst Nanoeng. 2020 Mar 9;6:23.
Gong L, et al. Front Oncol. 2020 Apr 24;10:461.
Pan Y, et al. Biosens Bioelectron. 2019 Apr 1;130:344-351.
Xu Z et al. Mol Cell. 2024 Dec 13:S1097-2765(24)00954-7. doi: 10.1016/j.molcel.2024.11.029.
Xu Z, et al.Mol Cell. 2025 Feb 6;85(3):490-505.e11. doi: 10.1016/j.molcel.2024.11.029.
Ren F,et al.Front Immunol. 2025 Feb 28;16:1513806. doi: 10.3389/fimmu.2025.1513806.
Ren F,et al.Front Immunol. 2025 Feb 28;16:1513806. doi: 10.3389/fimmu.2025.1513806.
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