In the wire constituting the LIN, which is one of the vehicle communication devices, disconnection of the wire or contact resistance of the circuit occurs due to vibration and aging of the vehicle. This affects the entire communication network and may have a significant impact on the safe driving of the vehicle as information is not transmitted. In this study, a LIN BUS circuit simulator was built on its own like a real car and measured with an automotive oscilloscope instead of a common method of measuring and diagnosing a circuit with a multimeter in the event of a LIN BUS circuit failure. Referring to the experimental results, it will be possible to diagnose faults in circuits efficiently and quickly.

Bursaphelenchus xylophilus (Bx) is the main plant-parasitic nematode of the Japanese Black Pine (Pinus thunbergii), Red Pine (Pinus densiflora) and Korean Pine (Pinus koraiensis) in the South Korea. Until now, the nematode morphological classification or PCR method using specific marker of Bx were used for the diagnosis of pine wilt disease. However, both methods have a disadvantage that these take a long time to confirm the result. Thus, these methods can not be used quickly at the newly damaged regions. For above the reasons, we had been developed the diagnostic method for Bx combining direct gDNA extraction buffer (DAP) with Recombinase Polymerase Amplification (RPA). This method is able to directly use mixed lysates extracted from Bx-infected pinewood by DAP buffer as gDNA template to RPA without another process for increase gDNA yield. Together, our method is able to detect Bx within 20 mins.

Until recently, molecular detection method for Bursaphelenchus xylophilus (Bx) infesting pine trees and killing themhas been developed several ways such as RFLP, Real-time PCR and LAMP. However, these were not only time-consumingprocess but also could not confirm the result in a short time. Furthermore, these methods also need thermo cycler orthermostat which are not portable and inexpensive. For above reasons, we had been developed the detection method forBx remaining in the pinewood chips without using electronic devices. In this study, we had used DUNT buffer that isable to extract genome DNA from Bx in the pinewood within 10 min and isothermal amplification that could be amplifiedthe specific DNA fragment of Bx at 37 ℃ for 10 min. As a result, our method is able to confirm the presence or absenceof Bx in pine trees within 20 min and could be used in the field as it does not require the electronic devices.

There are many other detection methods for Bursaphelenchus xylophilus. However, Baermann funnel method, PCR-based methods, which are laborious and time consuming processes that are unsuitable to rapid diagnose the Pine Wilt Disease (PWD) on the field. For these reasons, the aim of our experiment is not only to apply field diagnostic for pine wood nematode (PWN) but also to reduce total time for detection PWN in the pine trees by loop-mediated isothermal amplification (LAMP) with phosphate (Pi)-induced coloration reaction which could be yes or no answer for detection of PWN has not required UV detector but it just could be discriminated by naked eyes within 30 min. Genomic DNA was directly extracted from pine wood chips by Wood Chips Direct Lysis procedure which can be used for LAMP only after simple dilution. Our results suggest that LAMP-Pi detection method, simple and rapid method for detection of PWN, could be applied to the field diagnostic for PWD.

  The high degree of viscosity and the non-Newtonian fluid dynamics characterizes the process inside a glass furnace. Because the temperature is fluctuating in very short time-intervals, it is hard to determine that the status of its fluctuation is stable

A rapid and sensitive assay for specific detection and identification of barley yellow mosaic virus(BaYMV) was set up using the reverse transcriptase polymerase chain reaction(RT-PCR). A couple of primers was select to discriminate the viruses. PCR fragments of BaYMV(ca.0.9 kb) were obtained by using the method designed for BaYMV capsid protein. RT-PCR fragments were cloned with vector pT7 Blue and the resulting clones were sequenced. Capsid protein of BaYMV consisted of 297 amino acids and 891 nucleotides. The capsid protein sequence of BaYMV showed that 98% of nucleotides and 99% of amino acids homology.