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Streptozocin (Streptozotocin)

SKU: orb1308404

描述

Streptozotocin is a GLUT2-transported antibiotic that selectively induces pancreatic β-cell apoptosis via DNA alkylation. It is extensively used to generate experimental models of diabetes in vivo and to study β-cell toxicity in vitro. Due to its instability, fresh preparation in solution is required.

研究领域

Cell Biology

图片与验证

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关键属性

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CAS 号18883-66-4
MW265.2
纯度>97%
分子式C8H15N3O7
SMILES[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)(NC(N(N=O)C)=O)C=O
靶点DNA
溶解性Soluble in DMSO (up to 25 mg/ml) or in Water (up to 100 mg/ml)

客户验证数据

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反应性分布

最新实验

4 Results
稀释
样本
摘要
In vivo
Mouse
40 mg/kg
C57BL/6J mice
The Streptozotocin (STZ) is used to...
In vivo
Mouse
80 mg/kg
Blood and retinal tissues
STZ is dissolved in sodium citrate...
In vivo
Mouse
50 mg/kg
C57BL/6J mice
STZ is dissolved in 0.1 M...
In vivo
Mouse
55 mg/kg
Male C57BL/6 mice
Mice are fed a high‑fat diet...

生物活性

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靶点 IC50
DNA methylating (C1498 cells):1024 μg/mL|DNA methylating (K562 cells):904 μg/mL|DNA methylating (HL6 cells cells):11.7 μg/mL
体内
METHODS: Streptozocin (40 mg/kg in the 50 mM sodium citrate buffer (pH 4.5), ready to use) was administered intraperitoneally to C57BL/6 or CD-1 male mice once daily for five days. Normal food and 10% sucrose water were provided during the administration period, and 10% sucrose water was replaced with normal water on the sixth day. RESULTS: Repeated low doses of Streptozocin induced type 1 diabetes in mice. METHODS: Streptozocin (200 mg/kg in the 50 mM sodium citrate buffer (pH 4.5), ready to use) was administered to C57BL/6 or CD-1 male mice by a single intraperitoneal injection. Normal food and 10% sucrose water were provided after administration, and 10% sucrose water was replaced with normal water on the third day. RESULTS: A single high dose of Streptozocin induced type 1 diabetes in mice.
体外
METHODS: Rat β-insulinoma cells Rin-5F were treated with Streptozocin (1-10 mM) for 2-48 h. Cell viability was measured using MTT assay. RESULTS: Maximum inhibition (60-70%) was observed in cells treated with 10 mM Streptozocin for 24 h and 48 h. The cells were treated with Streptozocin (1-10 mM) for 2-48 h, and cell viability was measured by MTT assay. METHODS: Neural stem cells were treated with Streptozocin (2.5 mM) for 2 days and gene expression was detected using RT-qPCR. RESULTS: Streptozocin significantly reduced the relative expression level of GLUT3 mRNA by 46.4%, and did not affect the relative expression level of IR and GLUT1.
细胞研究
Streptozocin (STZ) stock solutions of 50 mg/mL in distilled Water (dWater) are freshly prepared for each experiment. Human and murine cell lines are cultured in triplicate in 96-well plates at a density of 2×104 cells/well in the absence (untreated control) or presence of various concentrations of ALX (20-3000 μg/mL) or STZ (1-3000 μg/mL) for 48 h at 37°C under a humidified atmosphere containing 5% CO2. Cells incubated in complete media including dWater in a final concentration of 0.1% served as control for solvent toxicity and cells incubated in complete medium are used as a control for the experiments. The effects of the tested drugs on tumor cell growth or viability are determined employing the MTT assay in accordance with the manufacturer's instructions. The IC50values (drug concentration that induces 50% inhibition of the cell growth) are calculated using the GraphPad Prism 4 program.

储存与操作

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储存-20°C
有效期12 months from date of receipt.
免责声明For research use only

别名

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Streptozotocin; U-9889

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质量保证

质量保证

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our 条款与条件和选购指南.

关键属性

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实验方案信息

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1 g
¥ 3,120.00
5 g
¥ 8,710.00
发货Usually dispatched within 5-10 working days
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