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3-sulphophthalic acid
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In order to study only the exosome-associated microRNAs and proteins, it is important to remove as many subcellular particles as possible from blood plasma or serum, particularly lipoprotein particles. Lipoproteins are the major lipid-based particles in the plasma and serum. It has been recently demonstrated that both high-density lipoproteins (HDLs) and low-density-density lipoproteins (LDLs) contain microRNAs. In order to deplete as much of these lipoproteins, which may cause false positive "hits" in analysis of exosome-associated microRNAs, we have developed the kit containing exosome precipitation solution and proprietory pre-clearing reagents to efficiently deplete lipoprotein particles from plasma or serum.
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文献和实验实验原理 Add a mixture of biotinylated monoclonal antibodies against non-DC cells to your starting sample. Add Depletion MyOne™ SA Dynabeads® and allow them to bind to the non-DCs during a short incubation. Separate
Isolate It All:siRNA • miRNA • Total RNA • Native Protein
Figure 5. Isolation of Total RNA and Protein from Different Tissues. Total RNA and protein were isolated from 4 different mouse tissues (~50 mg) with the mir Vana™ miRNA Isolation Kit (RNA only) or the mir Vana™ PARIS™ Kit. (A) Small RNA
Endothelial Cell Systems - Instructions For Use
. CC-4142/4180 EGLM™ SingleQuots® Kit, EGM® labeling SingleQuots® or EGLM™ -2 SingleQuot® Kit, EGM®-2 labeling SingleQuots® consisting of the following: 3.5128 mg/ml L-Cysteine (CC-4069) 5 ml 16.3963 mg/ml L-Isoleucine(CC-4070)2 ml 7.2064 mg/ml Myo
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