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S for proteomic analysis of early embryos enable research to be taken in novel directions in embryogenesis.BackgroundThe zebrafish has become a widely used vertebrate model system for which a large tool-box of genetic and cell biological methods has been established [1,2]. Research using zebrafish is further supported by the zebrafish sequencing project, which has facilitated the generation of mic
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Ental counterparts. We did not observe, however, distant invasion in U87MG tumors over-expressing galectin-1. The U87MG model is in fact weakly invasive in the brains of immunocompromized mice [33,34], while it is associated with pronounced neoangiogenesis processes [37]. Further work (e.g. viral transduction) with our patient-derivedToussaint et al. Molecular Cancer 2012, 11:32 http://www.molecul
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L antibodies made also rapidly clear to the clinicians that a reliable predictive factor for outcome was, in fact, lacking [3-7]. The introduction of K-RAS mutational status analysis allowed a reliable selection of resistant patients (i.e. those with mutated K-RAS). However not all K-RAS wildtype cases were also responders to anti-EGFR monoclonal antibodies. This observation made the need for furt
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Arabic wedding follows a huge number of rituals and also contains a lot of excitements. If you are searching assisting hands for your wedding then you can choose Jovial Events, one of the prominent Arabic wedding planners in Abu Dhabi. The team will fill your wedding with countless memorable moments and enjoyment along with following each and every ritual.






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Bryos In the early embryo, the cells forming the embryo proper constitute only a minor volume of the embryo compared to the large yolk cell (Fig. 1B). The abundance of yolk proteins interferes with any proteomic application that intends to target the cells of the embryo proper. The major yolk protein Vitellogenin, a phospholipo-glycoprotein,Page 1 of(page number not for citation purposes)BMC Devel
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Yolk removal. Embryos with yolk (Y) were analysed in comparison with embryos after one-step deyolking (D) or after two additional wash steps (W). A. Total protein amount per embryo as determined by DC protein assay (Bio-Rad). B. Coomassie stain (0.5 embryos loaded per lane). C. Western blot against Tubulin and MEK (0.5 embryos loaded per lane). While yolk proteins were efficiently depleted, recove
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Sical IPV in this study (35.5 ) is within the range of prevalence in some areas investigated in the WHO multi-country study across different cultures and socio-economic settings (30 -40 ) such as Namibia, Bangladesh, New Zealand, Thailand, Tanzania, Brazil, and Australia [23,29]. It is slightly lower than those reported among women attending general health practice in Ireland 39 [22], Sanandaj ci
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