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1.
Anal Biochem ; 433(2): 105-11, 2013 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-23085117

RESUMO

Western blots are used to specifically measure the relative quantities of proteins of interest in complex biological samples. Quantitative measurements can be subject to error due to process inconsistencies such as uneven protein transfer to the membrane. These non-sample-related variations need to be compensated for by an approach known as normalization. Two approaches to data normalization are commonly employed: housekeeping protein (HKP) normalization and total protein normalization (TPN). In this study, we evaluated the performance of Stain-Free technology as a novel TPN tool for Western blotting experiments in comparison with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a representative of the HKP normalization strategy. The target protein (TP) used for this study was MCM7, a DNA licensing replication factor, which was shown previously to be down-regulated by 20% in irradiated lymphoblastoid cell lines (LCLs). We studied the regulation of MCM7 with a multiplex Western blotting approach based on fluorescently labeled secondary antibodies and found that Stain-Free technology appears to be more reliable, more robust, and more sensitive to small effects of protein regulation when compared with HKP normalization with GAPDH. Stain-Free technology offers the additional advantages of providing checkpoints throughout the Western blotting process by allowing rapid visualization of gel separation and protein transfer.


Assuntos
Western Blotting/métodos , Proteínas de Ciclo Celular/química , Proteínas de Ligação a DNA/química , Gliceraldeído-3-Fosfato Desidrogenase (Fosforiladora)/química , Proteínas Nucleares/química , Western Blotting/normas , Proteínas de Ciclo Celular/análise , Linhagem Celular Tumoral , Proteínas de Ligação a DNA/análise , Gliceraldeído-3-Fosfato Desidrogenase (Fosforiladora)/análise , Humanos , Componente 7 do Complexo de Manutenção de Minicromossomo , Proteínas Nucleares/análise
2.
Electrophoresis ; 31(15): 2655-63, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20665923

RESUMO

We have developed a microfluidic system--microPrep--for subcellular fractionation of cell homogenates based on dielectrophoretic sorting. Separation of mitochondria isolated from a human lymphoblastoid cell line was monitored by fluorescence microscopy and further characterized by western blot analysis. Robust high throughput and continuous long-term operation for up to 60 h of the microPrep chip system with complex biological samples became feasible as a result of a comprehensive set of technical measures: (i) coating of the inner surfaces of the chip with BSA, (ii) application of mechanical actuators to induce periodic flow patterns, (iii) efficient cooling of the device to ensure integrity of organelle, (iv) a wide channel to provide for high fluidic throughput, and (v) integration of a serial arrangement of 10 dielectrophoretic deflector units to enable separation of samples with a high particle load without clogging. Hence, microPrep yields tens of micrograms of enriched and purified mitochondria within hours. Western blots of mitochondria fractions showed that contaminating endoplasmatic reticulum was reduced by a factor 6 when compared with samples prepared by state of the art centrifugation.


Assuntos
Fracionamento Celular/métodos , Eletroforese em Microchip/métodos , Mitocôndrias/química , Proteínas Mitocondriais/análise , Fracionamento Celular/instrumentação , Linhagem Celular Tumoral , Eletroforese em Microchip/instrumentação , Desenho de Equipamento , Humanos
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