Bespuiting van tomaten met Plantfood (19-22-16), 1953

<p><b>Copyright information:</b></p><p>Taken from "Cadmium triggers an integrated reprogramming of the metabolism of PCC6803, under the control of the Slr1738 regulator"</p><p>http://www.biomedcentral.com/1471-2164/8/350</p><p>BMC Genomics 2007;8():350-350.</p><p>Published online 2 Oct 2007</p><p>PMCID:PMC2190772.</p><p></p> indicated durations on solid BG11 medium with or without HO(3 mM), CdSO(50 μM), Co(NO)(350 μM), (NH)FeHCHO(350 μM) or ZnSO(350 μM or 776 μM). The spectra (normalized to light scattering at 800 nm) are displayed in panels A to F. These experiments were repeated three to five times

Cadmium triggers an integrated reprogramming of the metabolism of PCC6803, under the control of the Slr1738 regulator-2

<p><b>Copyright information:</b></p><p>Taken from "Cadmium triggers an integrated reprogramming of the metabolism of PCC6803, under the control of the Slr1738 regulator"</p><p>http://www.biomedcentral.com/1471-2164/8/350</p><p>BMC Genomics 2007;8():350-350.</p><p>Published online 2 Oct 2007</p><p>PMCID:PMC2190772.</p><p></p> indicated durations on solid BG11 medium with or without HO(3 mM), CdSO(50 μM), Co(NO)(350 μM), (NH)FeHCHO(350 μM) or ZnSO(350 μM or 776 μM). The spectra (normalized to light scattering at 800 nm) are displayed in panels A to F. These experiments were repeated three to five times

Cadmium triggers an integrated reprogramming of the metabolism of PCC6803, under the control of the Slr1738 regulator-0

<p><b>Copyright information:</b></p><p>Taken from "Cadmium triggers an integrated reprogramming of the metabolism of PCC6803, under the control of the Slr1738 regulator"</p><p>http://www.biomedcentral.com/1471-2164/8/350</p><p>BMC Genomics 2007;8():350-350.</p><p>Published online 2 Oct 2007</p><p>PMCID:PMC2190772.</p><p></p> 360 min.) prior to disruption. 5 μg of crude cell extracts were analyzed by Western blottings (Methods), using the antibodies directed against the indicated proteins

Standard Guidelines for the Chromosome-Centric Human Proteome Project

The objective of the international Chromosome-Centric Human Proteome Project (C-HPP) is to map and annotate all proteins encoded by the genes on each human chromosome. The C-HPP consortium was established to organize a collaborative network among the research teams responsible for protein mapping of individual chromosomes and to identify compelling biological and genetic mechanisms influencing colocated genes and their protein products. The C-HPP aims to foster the development of proteome analysis and integration of the findings from related molecular -omics technology platforms through collaborations among universities, industries, and private research groups. The C-HPP consortium leadership has elicited broad input for standard guidelines to manage these international efforts more efficiently by mobilizing existing resources and collaborative networks. The C-HPP guidelines set out the collaborative consensus of the C-HPP teams, introduce topics associated with experimental approaches, data production, quality control, treatment, and transparency of data, governance of the consortium, and collaborative benefits. A companion approach for the Biology and Disease-Driven HPP (B/D-HPP) component of the Human Proteome Project is currently being organized, building upon the Human Proteome Organization's organ-based and biofluid-based initiatives (www.hupo.org/research). The common application of these guidelines in the participating laboratories is expected to facilitate the goal of a comprehensive analysis of the human proteome