高效液相色谱仪期间核查方法研究

高效液相色谱仪做为强制检定仪器除按规定定期送法定检定机构进行检定外,在两次检定周期之间还需对使用频率高的仪器进行期间核查以维持设备校准状态的可信度.本文简述了期间核查的项目和方法,包括外观检查、输液系统检查、色谱柱和检测器性能检查及做好检查和处理结果的记录.     

中西医结合治疗羊传染性脓疱

2004年10月27日,我县王甫乡一养羊户的羊只发生以唇部皮肤呈菜花样增生、出血、溃烂为特征的疫病,畜主称之为"烂嘴病",该病传播快,发病率高,给养羊户造成严重的经济损失.笔者根据流行病学调查、临床症状诊断为羊传染性脓疱,采用中西医结合治疗,收到了较好的疗效.     

Adaptive optics revisited

From the earliest days and nights of telescopic astronomy, atmospheric turbulence has been a serious detriment to optical performance. The new technology of adaptive optics can overcome this problem by compensating for the wavefront distortion that results from turbulence. The result will be large gains in resolving power and limiting magnitude, closely approaching the theoretical limit. In other words, telescopic images will be very significantly sharpened. Rapid and accelerating progress is being made today by several groups. Adaptive optics, together with the closely related technology of active optics, seems certain to be utilized in large astronomical telescopes of the future. This may entail significant changes in telescope design.     

Sulfoxaflor and the sulfoximine insecticides: Chemistry,mode of action and basis for efficacy on resistant insects

The sulfoximines, as exemplified by sulfoxaflor ([N-[methyloxido[1-[6-(trifluoromethyl)-3-pyridinyl]ethyl]-λ⁴-sulfanylidene] cyanamide] represent a new class of insecticides. Sulfoxaflor exhibits a high degree of efficacy against a wide range of sap-feeding insects, including those resistant to neonicotinoids and other insecticides. Sulfoxaflor is an agonist at insect nicotinic acetylcholine receptors (nAChRs) and functions in a manner distinct from other insecticides acting at nAChRs. The sulfoximines also exhibit structure activity relationships (SAR) that are different from other nAChR agonists such as the neonicotinoids. This review summarizes the sulfoximine SAR, mode of action and the biochemistry underlying the observed efficacy on resistant insect pests, with a particular focus on sulfoxaflor.     

Single-molecule DNA sequencing of a viral genome

The full promise of human genomics will be realized only when the genomes of thousands of individuals can be sequenced for comparative analysis. A reference sequence enables the use of short read length. We report an amplification-free method for determining the nucleotide sequence of more than 280,000 individual DNA molecules simultaneously. A DNA polymerase adds labeled nucleotides to surface-immobilized primer-template duplexes in stepwise fashion, and the asynchronous growth of individual DNA molecules was monitored by fluorescence imaging. Read lengths of >25 bases and equivalent phred software program quality scores approaching 30 were achieved. We used this method to sequence the M13 virus to an average depth of >150x and with 100% coverage; thus, we resequenced the M13 genome with high-sensitivity mutation detection. This demonstrates a strategy for high-throughput low-cost resequencing.