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Please store the product under the recommended conditions in the Certificate of Analysis.
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货期:询盘
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MedChemExpress LLC
- CAS号:
5873-16-5
- 规格:
询盘
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Sulforhodamine G
CAS No. : 5873-16-5
MCE 国际站:Sulforhodamine G
产品活性:Sulforhodamine G 是一种具有宽动态范围的荧光染料。Sulforhodamine G 可用于蛋白质染色的研究。
研究领域:Others
作用靶点:Fluorescent Dye
In Vitro: Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).
Labeling of fluorescent internal protein:
A. Prepared of protein samples:
1. Protein samples to be analyzed are spiked with 0.1% of the total protein load of ALIS647 (ALIS internal standard) prior.
2. Protein sample is separated with 2-DE in the dark.
B. Purify Sulforhodamine G:
1. Sulforhodamine G (60% purity, 10 mg) dissolved in 100 mL of 1% v/v acetic acid to purify by RP chromatography.
2. Collect the pool with an absorbance maximum at 528 nm, lyophilized to dryness and stored as a dry powder at 47℃.
C. Stainning:
1. staining was performed in polypropylene staining dishes wrapped in aluminum foil to prevent photobleaching of the stains.
2. Sulforhodamine G staining is performed overnight in 35% methanol with a four-fold molar excess of dye: protein based on an average protein molecular weight of 50 kDa.
3. Following 4×15 min washes in 35% methanol and 2×15 min equilibrations in water.
4. Total protein and ALIS are visualized with a laser scanner using different channels.
5. Protein spots visualized using total protein stain (λex=532 nm) and ALIS (λex=633 nm) are quantified separately using 2-DE software, and statistical analysis.
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文献和实验Sulforhodamine B Assay and Chemosensitivity
The sulforhodamine B (SRB) assay was developed by Skehan and colleagues to measure drug-induced cytotoxicity and cell proliferation for large-scale drug-screening applications. Its principle is based on the ability of the protein dye
A variety of assays, and rationales for their use, exist to monitor viability and/or survival following cellular exposure to insult. Two commonly used in vitro assays are the sulforhodamine B assay and the clonogenic survival assay
一、样本准备 收集细胞,200 目筛网过滤,收集滤液,300g 离心 5 min,弃上清。 向细胞中加入适量细胞染色 buffer(或含1%BSA的PBS),用移液枪轻轻吹打细胞重悬。 二、细胞计数 用血球计数板或其他仪器对悬液进行计数后,调整细胞浓度约为 1 × 107/mL。 三、设置实验分组 根据实验设计,设置实验分组,每管加入 100μL 细胞悬液。 四、封闭 Fc 受体 封闭 Fc 受体能减少染色过程中的非特异性染色。 小鼠中,纯化的 CD16/CD32 单抗
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