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941.
Proteomic profiling and biomarker search are analytical tools as many other. Nevertheless, in the proteomic discovery phase considerable sample fractionation is inevitable before readout. Since these procedures are of notable complexity, proteomic tools need in particular analytical quality validation standards as prevail for other analytical methods. With acceptance of the rule of error propagation the values of imprecision and yield of each preparation step determine overall reproducibility and therewith information harvest of a propagated method series. Thereto, we examined recent proteomic reports with reproducibility data and with parallelization, and automation approaches. Based on the data available from literature it is highly probable, that at least a part of current proteomic platforms actually suffer from high technical variance.  相似文献   
942.
943.
  总被引:3,自引:0,他引:3  
Abstract. Pyrimidine dimer sites associated with the newly-synthesized DNA were detected during post-replication repair of DNA in UV-irradiated human fibroblasts. These pyrimidine dimer sites were inferred from a decrease in the molecular weight of pulse-labelled DNA after treatment with an extract of Micrococcus luteus containing UV-specific endonuclease activity. In DNA synthesized immediately after irradiation the frequency of these daughter strand dimer sites was 7–20% of that in the parental DNA. Such sites were found in fibroblasts from normal donors and from xeroderma pigmentosum patients (with defects in excision-repair or post-replication repair). They were excised from the DNA of normal cells. As the time between UV-irradiation and pulse-labelling was increased, the frequency of dimer sites associated with the labelled DNA decreased. If the pulse-label was delivered 6 h after irradiation of normal cells or excision-defective xeroderma pigmentosum cells, no dimer sites were detected in the labelled DNA. It has usually been assumed that daughter-strand dimer sites were the result of recombinational exchanges. The assay procedure used in these experiments and in similar experiments of others did not distinguish between labelled DNA containing pyrimidine dimers within the labelled section, and labelled DNA which did not contain pyrimidine dimers but was attached to unlabelled DNA which did contain dimers. The latter structures would arise during normal replication immediately following UV-irradiation of mammalian cells. Calculations are presented which suggest that a significant proportion and conceivably all of the dimer sites associated with the daughter strands may have arisen in this way, rather than from recombinational exchanges as has been generally assumed.  相似文献   
944.
945.
    
Wu  Zeming  Huang  Zhiqiang  Lehmann  Rainer  Zhao  Chunxia  Xu  Guowang 《Chromatographia》2009,69(1):23-32
  相似文献   
946.
947.
    
A convergent synthesis in which all trans double bonds were constructed by Wittig–Horner reactions produces dendrimers of the general structure 1 . With long-chain alkoxy residues on the periphery of the benzene rings, the first two generations display liquid crystalline behavior.  相似文献   
948.
    
In a 8-μL multichambered microreactor (the photo shows the components) material libraries can be produced in a simple manner through combinatorial hydrothermal synthesis. In a model experiment the synthesis of the zeolite TS-1 has been varied combinatorially. The resulting library is characterized directly by automated microdiffraction.  相似文献   
949.
    
Faster than with conventional solution-phase methods , mass spectrometry can be used to recognize the formation of noncovalent complexes. This is shown by the detection of the specific triple complex between an 18-residue zinc finger peptide from the gag protein p55 of HIV-1, Zn2+, and the oligodeoxynucleotide d(TTGTT) by MALDI-MS (see the spectrum). The results also indicate that MALDI mass spectra can qualitatively reflect solution-phase chemistry.  相似文献   
950.
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