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Anaspec/SensoLyte ® pNPP Alkaline Phosphatase Assay Kit *Colorimetric*/1 kit/AS-72146
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Anaspec/SensoLyte ® pNPP Alkaline Phosphatase Assay Kit *Colorimetric*/1 kit/AS-72146
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Anaspec
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AS-72146
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Description
Product NameSensoLyte ® pNPP Alkaline Phosphatase Assay Kit *Colorimetric*
Size1 kit
Catalog #AS-72146
US$$191

The change of alkaline phosphatase activity is involved in a variety of physiological and pathological events, such as bone development, bone-related diseases, gestation-related diseases and inflammatory bowel diseases. Alkaline phosphatase is also a popular enzyme conjugated with secondary antibody for ELISA. p-Nitrophenyl phosphate (pNPP) is proven to be an effective chromogenic substrate for alkaline phosphate. This SensoLyte® kit can be used to detect alkaline phosphatase activity in biological samples and alkaline phosphatase-based ELISA. The kit contains: pNPP chromogenic liquid substrate (absorption maximum = 405 nm upon dephosphorylation), Assay buffer, Stop solution, Alkaline phosphatase standard, “mix and read” assay protocol that is compatible with high throughput screening.

Kit size: 500 assays

Detailed InformationDatasheet
Material Safety Data Sheets (MSDS)
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蚂蚁淘(www.ebiomall.cn)是中国大陆目前唯一的生物医疗科研用品B2B跨境交易平台, 该平台由多位经验丰富的生物人和IT人负责运营。蚂蚁淘B2B模式是指客户有采购意向后在蚂蚁 淘搜索全球供应信息,找到合适的产品后在蚂蚁淘下单,然后蚂蚁淘的海外买手进行跨境采购、 运输到中国口岸,最后由蚂蚁淘国内团队报关运输给客户...
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两种质粒是可以同时进入同一个感受态细胞的,比如构建腺病毒载体时.但是要求两种质粒进入同一个感受态细胞,转化效率非常低,一般需要电转或者其他的特殊处理.
由于质粒的不兼容性,拥有同种复制子的质粒不能在同一细胞内稳定共存,经过几代的复制,会质粒丢失,所以并不是任何两个或两个以上质粒都可以在同一细胞内稳定存在,但是可以同时进入.
稳定转染的细胞株,就是转染后质粒可以稳定整合到基因组上不会因细胞分裂而丢失。区别于质粒瞬时转染不能长时间保留质粒在细胞里。
有人有用过吉凯的GV248慢病毒吗,关于胃癌方面的,小弟在构建LncRNA干扰的稳转胃癌细胞SGC-7901株,转想请问这种细胞株嘌呤霉素的筛选浓度是多少,如何进行筛选?
1、请教各位老师,转染质粒DNA的HepG2及HUH7细胞,如何筛选稳转细胞株
2、有限稀释法有没有protocol?
可以,除了单靶点外,该技术也可以进行多靶点基因敲除。
如题,需要对一株肝癌细胞构建稳转细胞株成默其中的一个基因,上海有哪家公司做这个效果比较好的呢?有知道的站友麻烦推荐一下谢谢。
稳转细胞系常用的方法有脂质体转染和慢病毒转染进行稳定株筛选,脂质体法筛单克隆时间耗时长,假阳性高,且效率低,大概只有1%。病毒转染得到稳定细胞株的效率高,只是步骤繁琐。
如果经费充足的话可以找公司包装病毒,如武汉的普健可以提供各种载体的构建及细胞株构建的技术服务。
刚刚到货的逆转录病毒载体,发现其中无GFP,请问大家用这种无荧光的载体包装病毒并转到细胞后,如何进行下一步的筛杀稳定转染细胞株的实验,只能通过其抗生素的抗性进行筛选,盲目挑选单克隆么?谢谢大家!
转入目的基因但为什么不表达mRNA
先提取RNA,反转录成cDNA,然后根据目的基因设计PCR引物,通过半定量RT-PCR确定目的基因表达.
正因为检测的是mRNA,所以要先反转录成cDNA才能PCR.
稳转细胞系常用的方法有质粒转染和慢病毒转染进行稳定株筛选,前者操作简单,但是成功率很低,费时,假阳性高,最后可能导致几个月的工作白干了,慢病毒稳定株筛选方法比较简单,并且慢病毒本身具有稳定整合入基因组的特性,没有假阳性,慢病毒包装可能相对比质粒构建难度大,如果经费充足可以直接找公司包毒的。
稳转株的制备_药物123
kahn922021-07-23
稳定转染的细胞株,就是转染后质粒可以稳定整合到基因组上不会因细胞分裂而丢失。区别于质粒瞬时转染不能长时间保留质粒在细胞里。
1.将外源基因插入慢病毒载体
2.将构建完成的载体与慢病毒包装质粒混合,共转染靶细胞
3.收集病毒液
4.用病毒液感染靶细胞
5.用载体上带的抗生素进行筛选,如果没有,可以用无限稀释法
6.获得稳转株
这个要看细胞的状态和蛋白表达特点。推荐了解“主细胞库”“工作细胞库”这两个名词。
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