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Katsuyuki Sakuma Noriyasu Nagai Mikiko Saito Jun Mizuno Shuichi Shoji 《IEEJ Transactions on Electrical and Electronic Engineering》2009,4(3):339-344
This paper describes a simplified vertical interconnection process for three-dimensional (3D) chip stacking. The unique feature of this new process is that the conductive filling material in the through-silicon-vias (TSVs), the microbumps, and the interconnection materials are all fabricated in one processing stage. All of the steps can be performed with the same piece of equipment. Prototype chips with 20-µm-pitch vertical interconnections have been demonstrated successfully. By using this technique, 75-µm deep high-aspect-ratio vias can be completely filled without voids using Ni electroplating and uniform 20-µm-pitch microbumps that are 4-µm tall have been fabricated using Sn-Cu electroplating. Copyright © 2009 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc. 相似文献
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Tomoaki Fukunaga Kamonchai Cha‐aim Yuki Hirakawa Ryota Sakai Takao Kitagawa Mikiko Nakamura Sanom Nonklang Hisashi Hoshida Rinji Akada 《Yeast (Chichester, England)》2013,30(6):243-253
Recombinant DNAs are traditionally constructed using Escherichia coli plasmids. In the yeast Saccharomyces cerevisiae, chromosomal gene targeting is a common technique, implying that the yeast homologous recombination system could be applied for recombinant DNA construction. In an attempt to use a S. cerevisiae chromosome for recombinant DNA construction, we selected the single ura3Δ0 locus as a gene targeting site. By selecting this single locus, repeated recombination using the surrounding URA3 sequences can be performed. The recombination system described here has several advantages over the conventional plasmid system, as it provides a method to confirm the selection of correct recombinants because transformation of the same locus replaces the pre‐existing selection marker, resulting in the loss of the marker in successful recombinations. In addition, the constructed strains can serve as both PCR templates and hosts for preparing subsequent recombinant strains. Using this method, several yeast strains that contained selection markers, promoters, terminators and target genes at the ura3Δ0 locus were successfully generated. The system described here can potentially be applied for the construction of any recombinant DNA without the requirement for manipulations in E. coli. Interestingly, we unexpectedly found that several G/C‐rich sequences used for fusion PCR lowered gene expression when located adjacent to the start codon. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
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Intrinsic viscosity, osmotic second virial coefficient and light scattering of the BmAnBm and AmBnAm copolymers (A, styrene monomeric unit; B, p-chlorostyrene monomeric unit, m and n denote the number of units) in cumene which is a good solvent for polystyrene but a θ solvent for poly(p-chlorostyrene) at 59.0°C, were studied over the temperature range 65° to 15°C. The results suggested that conformational transition from a random coil form to a segregated form occurs at a critical temperature which appears to be in the range 40° to 30°C, depending on the composition, molecular weight and structure of the block copolymers; the θ condition could not be attained by cooling the block copolymer solutions, and micelle formations due to intermolecular associations were found in some cases below the transition temperature. 相似文献
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Various types of embryoid body (EB) that were formed from mouse embryonic stem (ES) cells under various culture conditions were characterized in terms of gene expression pattern to estimate the differentiation status of the bodies. The gene expression of typical markers (i.e., GATA-4, GATA-6, transthyretin [TTR], alpha-fetoprotein [AFP], Nkx2.5, and alpha-myosin heavy chain [alpha-MHC]) was quantitatively analyzed in various types of EB, and the gene expression pattern of those marker genes was graphically shown for each EB. The gene expression pattern accurately represented the differentiation status of the EBs. The gene expression pattern indicated that the Nkx2.5 and alpha-MHC genes were highly expressed in the EBs formed from 1000 ES cells in a low-adherence 96-well plate. By transferring the EBs into an attachment culture, cardiomyocytes were more efficiently generated in the outgrowth of the EBs. When we increased the seeding cell number from 1000 to 4000 ES cells, the gene expression pattern changed, that is, the expression levels of the TTR and AFP genes increased, whereas those of the Nkx2.5 and alpha-MHC genes decreased, and the trend of differentiation changed from cardiomyogenesis to visceral yolk-sac-like structure formation. 相似文献
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