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Improved Yeast Expression System by Could-Clone
It is well known that there are three types of commonly used systems in the field of gene engineering, including prokaryotic expression system (Escherichia coli expression system, also called E. coli expression system), yeast expression system (Pichia P. expression system) and mammalian cell expression system. The prokaryotic expression system is widely used because of the advantages of simple operation, low cost and high expression. But at the same time, prokaryotic expression system also has some shortcomings, such as it is prone to form of inclusion body, has no posttranslational processing and so on In order to avoid the shortage of prokaryotic expression system itself, Cloud-Clo......
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One Hot Spot in Cardiovascular Diseases-ANGs
It is reported by World Health Organization (WHO) that cardiovascular disease has become the leading cause of death. From the statistical data of 2008, death caused by cardiovascular disease is 30% of global death toll, and it is predicted that the ratio will increased by 18% in 2030. Due to the significant impact of this diseases on human being, researchers all over the world had pay persistent attention on it. Recently, lots of reports, which are about a group of peptides, angiotesin (ANG) , are published. Regarding to these peptides, our company had developed related reagents, so, they could be used by researchers to facilitate their research. ANGs is a group of hormone consist of ......
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Processing of Common Samples in Elisa
ELISAis a rapid,sensitive, accurate and reliable quantitative analysis method. Samplepreparation plays a pivotal role in a successful ELISAexperiment. At the beginning of collecting sample for ELISA, we might have a few problems. The common samples used for ELISA include blood(serum, plasma), tissue homogenates, cell lysatesand cell culture supernatants, etc. Manyfactors will have influence on the results of ELISA experiment, such as sampling time, processing, storage, etc.Now we introduce sample processing methods for reference.1.BloodAfter collecting, blood should be processed as soon as possible to separate serum (plasma) from whole blood.What’s the difference between serum and pl......
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mini kit- less sample, higher sensitivity
Elisa is a rapid, sensitive and accurate quantitative analysis method. It will need 100ul of sample for detection, while sometimes it’s just hard to get enough samples, especially when the concentration of target protein in the samples is low (such as: all kinds of cytokines). Then the normal ELISA kit will not be suitable. Now Cloud-Clone Corp. has developed Mini ELISA kits which require less samples (25ul~50ul), with the same procedure and experimental time, and its result is the same or even better than conventional kits. Now let’s take SEA079Mu (ELISA Kit for Interleukin 6 (IL6)) and MEA079Mu (Mini ELISA Kit for Interleukin 6 (IL6)) as an example to compare the whole process. T......
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Fitting of Standard Curve of Competitive Inhibition ELISA
As we know, for antigens with multiple epitopes, double sandwich ELISA (Double Sandwich ELISA) can be applied to the quantitative detection of target antigens or antibodies. While for small molecule or hapten, as lacking of more than two binding sites for double sandwich detection, double sandwich method is not suitable. In this case, competitive inhibition method can be applied to detect target molecules. Competitive inhibition ELISA also can be called blocking ELISA, its main principle is the competive binding of the antigens within the samples and the certain amount of labeled-antigens with antibody on the solid-phase. The more amount of antigen in samples, the less labeled antigen ......
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Why the samples′ OD is low in Elisa
In ELISA experiments, researchers often encounter samples with low OD, including serum, plasma, tissue homogenate, cell lysate, etc. Assuming the customer's operation is right, the standard curve is also good, in this situation the reasons can be analyzed in two ways. On one hand, the content of the sample itself can be detected, but some operations cause the samples measured value become out of the detection range of Elisa kit; On the other hand, low concentration of analyte in the sample itself. Following we’ll analyze in these two aspects and raise their solutions. 1. When the content of target molecules itself can be detected, what factors may cause low measured value......