Cleanascite™ LX - For Lipemic Serum/Plasma Clarification
货号：LX155-10
品牌：Biotech Support Group
产品特性
用于脂血血清/血浆的澄清
有效替代chlorinated/fluorinated hydrocarbons
基于固相技术研发
| 规格 | 价格 |
|---|---|
| 10 mL | ￥咨询 |
产品咨询：info@biopcr.com
产品订购：sales@biopcr.com
技术支持：tech@biopcr.com
服务热线：400-860-6200
详细介绍
产品名称：Cleanascite™ LX - For Lipemic Serum/Plasma Clarification
别名：Cleanascite™ LX脂血血清/血浆澄清试剂；Cleanascite LX脂血血清和血浆澄清试剂
Cleanascite™ LX - For Lipemic Serum/Plasma Clarification
用于脂血血清/血浆澄清试剂
• 可有效替代chlorinated/fluorinated hydrocarbons（如氟利昂）
• 基于固相技术研发，相关技术已在70余篇不同应用领域的出版物中被引用
• 正在研究作为LipoClear的替代品
Cleanascite™ LX is supplied as an aqueous suspension of non-ionic adsorbent in DI water, pH 8.0. After centrifugation, the pellet is 1/2 of the total volume and the supernatant is 1/2 of the total volume.
操作步骤
Lipid types and amounts can vary greatly, so the ratios shown are only intended to provide general guidance.
1. Resuspend CleanasciteTM LX by gentle shaking. Excessive shaking may cause foaming. It should be completely resuspended prior to use.
2. Add CleanasciteTM LX to the sample at minimum 1:3 (or alternative higher, up to 1:1) ratio. Mix the sample by gentle shaking for 20 minutes.
3. Micro-centrifugesampleat8,000rpm’s(5,000xg)for10minutes.
4. Carefully aspirate supernatant for analysis.
Optimization. Different sample volumes are easily scaled. Volume ratio can be adjusted up or down as required to remove the amount of impurities present.
返回列表
用于脂血血清/血浆澄清试剂
• 可有效替代chlorinated/fluorinated hydrocarbons（如氟利昂）
• 基于固相技术研发，相关技术已在70余篇不同应用领域的出版物中被引用
• 正在研究作为LipoClear的替代品
Cleanascite™ LX is supplied as an aqueous suspension of non-ionic adsorbent in DI water, pH 8.0. After centrifugation, the pellet is 1/2 of the total volume and the supernatant is 1/2 of the total volume.
操作步骤
Lipid types and amounts can vary greatly, so the ratios shown are only intended to provide general guidance.
1. Resuspend CleanasciteTM LX by gentle shaking. Excessive shaking may cause foaming. It should be completely resuspended prior to use.
2. Add CleanasciteTM LX to the sample at minimum 1:3 (or alternative higher, up to 1:1) ratio. Mix the sample by gentle shaking for 20 minutes.
3. Micro-centrifugesampleat8,000rpm’s(5,000xg)for10minutes.
4. Carefully aspirate supernatant for analysis.
Optimization. Different sample volumes are easily scaled. Volume ratio can be adjusted up or down as required to remove the amount of impurities present.
