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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
低温
- 库存:
现货
- 供应商:
上海善然生物科技有限公司
- 规格:
250G
琼脂糖
Agarose
BioReagent, for molecular biology, low EEO
产品名称
Analysis Note
The following is a list of properties associated with our agaroses:
Sulfate content - used as an indicator of purity, since sulfate is the major ionic group present.
Gel strength - the force that must be applied to a gel to cause it to fracture.
Gel point - the temperature at which an aqueous agarose solution forms a gel as it cools. Agarose solutions exhibit hysteresis in the liquid-to-gel transition - that is, their gel point is not the same as their melting temperature.
Electroendosmosis (EEO) - a movement of liquid through the gel. Anionic groups in an agarose gel are affixed to the matrix and cannot move, but dissociable counter cations can migrate toward the cathode in the matrix, giving rise to EEO. Since electrophoretic movement of biopolymers is usually toward the anode, EEO can disrupt separations because of internal convection.
Application
常规琼脂糖是通过凝胶电泳或印迹(Northern 或 Southern)进行日常核酸分析的理想选择,还适用于蛋白质应用,例如 Ouchterlony 免疫扩散和放射状免疫扩散 (RID)。含少量溴化乙锭和 SYBR Green 背景染料。
性质
| Related Categories | Agarose, Agarose Gel, Core Bioreagents, Life Science Reagents for Cloning, Life Science Reagents for DNA/RNA Electrophoresis, |
| grade | for molecular biology |
| product line | BioReagent |
| impurities | ≤10% moisture content |
| EEO | 0.09-0.13 |
| transition temp | gel point 36 °C (1.5% gel, ± 1.5 °C) |
| gel strength | ≥1200 g/cm2 (1% gel) |
| foreign activity | DNase, RNase, none detected |
| G9752-500G | 阿拉伯树胶 |
| 95904-1KG-F | PEG 4000 |
| M3671-50G | 无水MES |
| P7545-25G | 胰酶 |
| DN25-100MG | 脱氧核糖核酸酶 I |
| A9539-250G | 琼脂糖 |
| T1503-5KG | Tris 碱 |
| E5134-5KG | EDTA-Na2 |
| 52365-250G | CTAB |
| 62476-500G-F | 氯化锂 |
| 31650-250G | 氯化锌 |
| PVP40-500G | PVP40 |
| S5881-1KG | 颗粒氢氧化钠 |
| 217263-250G | 硫代硫酸钠 |
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文献和实验Tris-乙酸盐 1mmol/L EDTA 0.8%琼脂糖凝胶: 琼脂糖 0.8g TAE 100ml 器械 250ml锥形瓶+纸盖子+棉线绳 50ml量筒 白枪头 30μl枪 5μl枪 微波炉 电泳仪(梳子,制胶板) 凝胶成像仪 准备 1. 250ml锥形瓶,超生清洗,烘干. 2. 打开电子天平,预热. 3. 清洗制胶板,梳子,电泳槽. 步骤 1. 按配方配制TAE
二、仪器及试剂 1. 仪器及耗材: 水平电泳槽、电泳仪、凝胶成像分析系统、微波炉、微量移液器、透明胶带、点样板或parafilm、100ml或250ml锥形瓶、量筒、吸头等。 2. 试剂及配制: (1)50×TAE缓冲液的配制:2 mol/LTris-乙酸,0.05 mol/L EDTA(pH8.0) 配制1000 ml Tris242 g 冰乙酸57.1 ml 0.5 mol/L EDTA100 ml 加入600 ml 去离子水后搅拌溶解,将溶液定容
与模具之间留1mm空间。 2、称取DNA电泳用琼脂糖0.8g放入250ml的三角烧杯中,加入100ml 1×TAE缓冲液,混匀后,将烧瓶置于电炉上,加热煮沸,直至琼脂糖完全溶解。 3、关闭电炉,取下三角烧瓶,将其置室温下冷却至70℃左右(手握烧瓶可以耐受),再加入溴化乙锭(10mg/ml)5μl,混匀后,即将凝胶溶液倒入胶板铺板。本实验所用制胶板约需胶液100ml。 4、室温下待凝胶完全凝固,需时约30分钟,揭去二端胶布,拔出梳齿,将胶板放入电泳槽中
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