• 제목/요약/키워드: 4D-Media

검색결과 1,194건 처리시간 0.026초

딥러닝 기반 문화재 영상에 대한 4 배 및 8 배 초해상화 (Deep Learning based x4 and x8 Super-Resolution for Cultural Property Images)

  • 손채연;김수예;김주영;김문철
    • 한국방송∙미디어공학회:학술대회논문집
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    • 한국방송∙미디어공학회 2020년도 추계학술대회
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    • pp.118-122
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    • 2020
  • 문화재 영상 데이터는 방대한 양으로 인해 고해상도로 모두 저장이 어렵거나 시간이 지나 상대적으로 화질이 낮은 영상들이 다수 존재하기에 초해상화가 필요한 상황이 많다. 따라서 본 논문에서 처음으로 문화재 영상에 특화된 4 배 및 8 배 딥러닝 기반 초해상화 방식을 제안한다. 문화재 영상 데이터는 배경이 단조롭고 물체가 영상 중간에 위치한다는 특징이 있어 이를 고려해 중간 부분에서만 패치를 추출하는 방식을 적용하여 의미 있는 패치로 학습이 되도록 한다. 또 자연 영상 데이터 셋인 DIV2K 를 사용해 학습하는 방식과 직접 구성한 문화재 데이터 셋을 이용해 학습하는 방식, 그 둘을 적절히 함께 사용하여 학습하는 전이 학습 방법까지 세 가지로 학습하여 초해상화의 성능을 향상시키는 방법을 제안한다. 그 결과, 쌍삼차 보간법(Bicubic interpolation)보다 4 배 초해상화에서는 약 1.25dB, 8 배 초해상화에서는 약 1.26dB 의 성능 개선을 확인하였으며, 단순 DIV2K 로 학습한 방식보다는 4 배에서는 0.06dB, 8 배에서는 0.17dB 의 성능 개선을 확인하였다.

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페놀계 고농도 유기성 폐수의 생물학적 고도처리 운전인자 (Operation Parameters on Biological Advanced Treatment of Phenolic High-Strength Wastewater)

  • 홍성동;박철휘
    • 대한환경공학회지
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    • 제22권4호
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    • pp.797-806
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    • 2000
  • 본 연구는 탄소원으로서 페놀과 공동기질로서 글루코스를 합유한 인공합성폐수를 만들어 실험실 규모의 UASB(Upflow Anaerobic Sludge Blanket) - PBR(Packed Bed Reactor) 공정을 운전하면서 페놀의 유일한 탄소원으로서의 이용특성과 공동기질로서 글루코스를 주입한 경우의 이용특성, 미생물의 활성도 및 질소의 동시제거 가능성에 대한 연구를 수행하였다. 실험결과 페놀올 유일한 탄소원으로 주입한 경우 페놀유입농도 600 mg/L에서도 페놀제거율 99% 이상, SCOD 2100 mg/L 농도에서 제거율 93% 이상을 보였다. 조내 미생물의 량은(VSS) 약 20 g이었고 이때 미생물의 활성도는 $0.112g\;phenol/g\;VSS{\cdot}d$이었고 SCOD 제거율은 $0.351g\;SCOD/g\;VSS{\cdot}d$이며 가스발생율은 $0.115L/g\;VSS{\cdot}d$, 메탄가스의 함유율은 70%로 나타났다. 공동기질로 페놀파 글루코스를 주입한 경우 페놀유입농도 760 mg/L하에서 페놀제거율 98% 이상, SCOD 4300 mg/L 농도에서 제거율 90% 이상을 보였다. 조내 미생물의 량은(VSS) 약 20 g이었고 이때 미생물의 활성도는 $0.135g\;phenol/g\;VSS{\cdot}d$이었고 SCOD 제거율은 $0.696g\;SCOD/g\;VSS{\cdot}d$이며 가스발생율은 $0.257L/g\;VSS{\cdot}d$. 메탄가스의 함유율은 70%로 나타났다. 회분실험결과 페놀농도 1600 mg/L 이상의 농도에서 활성의 저해를 받았으며 메탄화반응과 탈질반응이 동시에 일어나는 것으로 관찰되었다. 질산화는 수리학적 체류시간 24시간으로 하여 암모니아성 질소 $0.038kg\;NH_4-N/m^3-media{\cdot}d$ 부하조건과 유입수내 페놀농도 10~12 mg/L, SCOD 200~500 mg/L 조건하에서 저해를 받지 않고 90% 이상의 질산화율을 보였고 페놀의 제거효율은 98% 이상을 보였다.

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Rabbit Antibody Raised against Murine Cyclin D3 Protein Overexpressed in Bacterial System

  • Jun, Do-Youn;Kim, Mi-Kyung;Kim, Young-Ho
    • Journal of Microbiology and Biotechnology
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    • 제6권6호
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    • pp.474-481
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    • 1996
  • Since the commercially available rabbit anti-cyclin D3, generated from c-terminal 16 amino acid residues which are common to human and murine cyclin D3, is highly cross-reactive with many other cellular proteins of mouse, a new rabbit polyclonal anti-cyclin D3 has been raised by using murine cyclin D3 protein expressed at a high level in Escherichia coli as the immunogen. To express murine cyclin D3 protein in E. coli, the cyclin D3 cDNA fragment encoding c-terminal 236 amino acid residues obtained by polymerase chain reaction (PCR) was inserted into the NcoI/BamHI site of protein expression vector, pET 3d. Molecular mass of the cyclin D3 overexpressed in the presence of IPTG (Isopropyl $\beta$-D-thiogalactopyranoside) was approximately 26 kDa as calculated from the reading frame on the DNA sequence, and the protein was insoluble and mainly localized in the inclusion bodies that could be easily purified from the other cellular soluble proteins. When renaturation was performed following denaturation of the insoluble cyclin D3 protein in the inclusion bodies using guanidine hydrochloride, 4.4 mg of soluble form of cyclin D3 protein was produced from the transformant cultured in 100ml of LB media under the optimum conditions. Four-hundred micrograms of the soluble form of cyclin D3 protein was used for each immunization of a rabbit. When the antiserum obtained 2 weeks after tertiary immunization was applied to Western blot analysis, it was able to detect 33 kDa cyclin D3 protein in both murine lymphoma cell line BW5147.G.1.4 and human Jurkat T cells at 3,000-fold dilution with higher specificity to murine cyclin D3, demonstrating that the new rabbit polyclonal anti-murine cyclin D3 generated against c-terminal 236 amino acid residues more specifically recognizes murine cyclin D3 protein than does the commercially available rabbit polyclonal antibody raised against c-terminal 16 amino acids residues.

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재구성 정합 회로를 이용한 평판형 이중 모드 안테나 설계 (Design of a Dual-Mode Planar Antenna Using a Reconfigurable Matching Network)

  • 김윤건;계영철;추호성
    • 한국전자파학회논문지
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    • 제23권12호
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    • pp.1337-1342
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    • 2012
  • 본 논문에서는 RF 스위치 역할을 하는 핀-다이오드를 이용하여 정합 회로의 형상을 변경하는 새로운 형태의 재구성 안테나를 제안하였다. 개발된 안테나는 HSDPA 대역(2.1~2.2 GHz), WiBro WiFi 대역(2.3~2.5 GHz)에서 Mode 1과 Mode 2의 두 가지 모드로 동작할 수 있도록 하였으며, polyarcylate 기판의 양면을 이용하여 제작 및 측정을 하였다. 측정 결과, Mode 1과 Mode 2의 동작 주파수에서 547 MHz($S_{11}$ <-3 dB, 2.035~2.582 GHz), 600 MHz($S_{11}$ <-3 dB, 2.2~2.8 GHz)의 대역폭을 보였으며, 각각 -4.4 dBi, -4.5 dBi의 x-y 평면 평균 수직 복사 성능을 보였다.

Sodium butyrate와 sodium pyruvate 첨가에 의한 hCTLA4Ig 생산성 증대 (Enhanced Production of hCTLA4Ig by Adding Sodium Butyrate and Sodium Pyruvate)

  • 유미희;김수진;권준영;남형진;김동일
    • KSBB Journal
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    • 제26권5호
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    • pp.386-392
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    • 2011
  • Human cytotoxic T-lymphocyte antigen 4-immunoglobulin (hCTLA4Ig), an immunosuppressive agent, was expressed in transgenic rice cells using RAmy3D promoter and RAmy1A signal peptide for the inducible production and secretion into culture media by sugar depletion. In this study, sodium butyrate was used as a small molecular enhancer (SME) to enhance the production of hCTLA4Ig in transgenic rice cell suspension cultures. When 1 mM sodium butyrate was added in sugar-free media, relative viability was not reduced, while the productivity was improved 1.3-fold. In addition, by supplementing 87 mM sodium pyruvate as an alternative energy source during the production phase, death rate of the cells was decreased. When sodium pyruvate was not added, most cells became dead at day 6. However, by adding sodium pyruvate, 18% of viability can be maintained until day 10 and the production of hCTLA4Ig was enhanced 1.4-fold. When the combination of sodium pyruvate and sodium butyrate at optimum concentrations was added, the highest viability and hCTLA4Ig production could be obtained. The highest level of hCTLA4Ig reached up to 35 mg/L at day 10.

Effect of stocker management program on beef cattle skeletal muscle growth characteristics, satellite cell activity, and paracrine signaling impact on preadipocyte differentiation

  • Vaughn, Mathew A.;Lancaster, Phillip A.;Roden, Kelly C.;Sharman, Evin D.;Krehbiel, Clinton R.;Horn, Gerald W.;Starkey, Jessica D.
    • Journal of Animal Science and Technology
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    • 제61권5호
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    • pp.260-271
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    • 2019
  • The objective of this study was to determine the effect of different stocker management programs on skeletal muscle development and growth characteristics, satellite cell (SC) activity in growing-finishing beef cattle as well as the effects of SC-conditioned media on preadipocyte gene expression and differentiation. Fall-weaned Angus steers (n = 76; $258{\pm}28kg$) were randomly assigned to 1 of 4 stocker production systems: 1) grazing dormant native range (NR) supplemented with a 40% CP cottonseed meal-based supplement ($1.02kg{\cdot}steer^{-1}{\cdot}d^{-1}$) followed by long-season summer grazing (CON, 0.46 kg/d); 2) grazing dormant NR supplemented with a ground corn and soybean meal-based supplement fed at 1% of BW followed by short-season summer grazing (CORN, 0.61 kg/d); 3) grazing winter wheat pasture (WP) at high stocking density (3.21 steers/ha) to achieve a moderate rate of gain (LGWP, 0.83 kg/d); and 4) grazing winter WP at low stocking density (0.99 steers/ha) to achieve a high rate of gain (HGWP, 1.29 kg/d). At the end of the stocker (intermediate harvest, IH) and finishing (final harvest, FH) phases, 4 steers / treatment were harvested and longissimus muscles (LM) sampled for cryohistological immunofluorescence analysis and SC culture assays. At IH, WP steers had greater LM fiber cross-sectional area than NR steers; however, at FH, the opposite was observed (p < 0.0001). At IH, CORN steers had the lowest Myf-5+:Pax7+ SC density (p = 0.020), while LGWP steers had the most Pax7+ SC (p = 0.043). At FH, CON steers had the highest LM capillary density (p = 0.003) and their cultured SC differentiated more readily than all other treatments (p = 0.017). At FH, Pax7 mRNA was more abundant in 14 d-old SC cultures from HGWP cattle (p = 0.03). Preadipocytes exposed to culture media from proliferating SC cultures from WP cattle isolated at FH had more $PPAR{\gamma}$ (p = 0.037) and less FABP4 (p = 0.030) mRNA expression compared with NR cattle. These data suggest that different stocker management strategies can impact skeletal muscle growth, SC function, and potentially impact marbling development in growing-finishing beef cattle.

펄프 및 제지공장 폐수의 처리에 관한 미생물학적 연구 2 (Microbiological Studies on the Treatment of Waste Liquer from Plup and Paper Industries(II))

  • 홍순우;강영화
    • 미생물학회지
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    • 제12권1호
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    • pp.31-36
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    • 1974
  • Four strains of yeasts were chosen from those isolated previously, and a strain from 160 isolates collected in this year were examined for the treatment of pulp waste liquor. Experiments about optimum nutrient condition, composition of cells, and reduction of B.O.D. on the "S" pulp industry waste liquor were performed with 5 strains. 1. The isolates(strain 112) was identified as Candida utilis. 2. The optium concentration of 4 components of nutrients were ($NH_4$)$SO_2$lg/l, yeast extract 70mg/l, $KH_2PO_4$ 300mg/l, and $MgSO_4{\ddot}7H_2O$ 500mg/l. 3. Specific growth ratio of Candida utilis KYRI 112 was 0.48/hr at optimum nutrient media and the yield was 0.45%(V/V). 4. Endomycopsis capsularis KYRI 613 contained more crude protein than the most of commercial yeasts. 5. The B.O.D. of waste liquor was reduced ro 20% of its value by the culture.e culture.

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Bacillus sphaericus ts-D1200 단백질의 전기영동적 분석 (Electrophoretic Analysis of Total Proteins in Bacillus sphaericus ts-Dl290)

  • 서정희;이형환;김영희
    • 한국미생물·생명공학회지
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    • 제18권5호
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    • pp.541-546
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    • 1990
  • Bacillus sphaericus ts-D1290 치사돌연변이주의 특성을 연구하기 위하여 제한온도와 허용온도에서 생산하는 단백질의 차이점을 연구하였고, 모기유충에서 생산하는 단백질을 분리하여 모기유충에 치사되는지를 조사하였다. ts-D1290 균주를 $42^{\circ}C$에서 배양했을 때는 $30^{\circ}C$ 배양보다 균체의 단백질 함량이 약 1/5로 감소하였고, $42^{\circ}C$에서 4시간 배양후 $30^{\circ}C$로 배양하였들 때는 약 1/3로 감소하였다. 그리고 단백질 패천은 ts-D1290 균주를 $42^{\circ}C$에서 전배양 후 $30^{\circ}C$로 하강 배양하였을 때는 $30^{\circ}C$에서 전배야하여 $42^{\circ}C$로 상승배양하였을 때와는 달라 분자량 221kd 단백질이 나타나지 않았지만 분자량 150kd 단백질은 $30^{\circ}C$ 전 배양하였을 때와 같이 현저하게 나타났다.

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생쥐난의 체외 배양에서 인간난포액과 표피 성장 인자가 난성숙에 미치는 영향 (The Effect of E.G.F. and Human Follicular fluid on the Maturation of Mouse Oocytes in in vitro Culture)

  • 민부기
    • Clinical and Experimental Reproductive Medicine
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    • 제20권2호
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    • pp.157-160
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    • 1993
  • The human follicular f1uids(F.F.) may be considered to contribute the maturation of the oocytes on the in vitro culture. To investigate the effects of epidermal growth factor (E.G.F.), which is present in mature and immature follicular fluids, we had experiments of mouse oocytes maturation in vitro. The endpoints assayed were rated as percentage of oocytes undergoing germinal vesicle breakdown(G.V.B.D.) and polar body(P.B.) formation at 12 hours after in vitro culture. The rates of G.B.B.D. were 87% in mature F.F. 68% in immature F.F. and 78% in Ham's F-10 medium respectively. And overall the mature F.F. seem to stimulate on in vitro oocyte maturation compared with either immature F.F. or Ham's F-10 medium. As the concentration of addition of E.G.F. in immature F.F., the rates of G.V.B.D. and P.B. formation were 82 %, 23% in addition with 2 ng/ml while 84%, 32% in addition with 4 ng/ml respectivly. And at the concentration of addition of E.G.F. in Ham's F-10 media as well, the rates of G.V.B.D. and P.B. formation were 84%, 40% and 82%, 44% in addition with each 2ng, 4ng. AccordinglY there was no influence on the oocytes maturation at the addition of E.G.F. to each immature F.F. and Ham's F-10 medium. In conclusion, the E.G.F. is not able to induce oocyte maturation independent of it's effects in immature F.F. and Ham's F-10 media.

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이온교환수지를 이용한 새로운 암로디핀 복합체 개발 (Development of New Amlodipine Complex using Ion Exchange Resin)

  • 정상영;안기영;안건석;길영식;황성주
    • Journal of Pharmaceutical Investigation
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    • 제38권1호
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    • pp.9-14
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    • 2008
  • Cation exchange resin complex of amlodipine free base has been investigated to improve the stability and dissolution profile. The complex was prepared by reacting amlodipine solution with activated cation exchange resin, and amlodipine content in the complex was 31.6% calculated by HPLC determination. Its product was not physical mixture but the complex formed by ionic bond, which was identified by microscope system, differential scanning calorimetry and X-ray diffractometry. Each tablet containing amlodipine free base(I) and its complex(II) was prepared for the accelerated stability test ($40^{\circ}C$, 75%RH) and dissolution test in the pH 1.2 buffer solution and purified water media. Dissolution patterns of formulation II in both media were similar to those of $Norvasc^{(R)}$ tablet, but the pattern of formulation I in purified water was different. After 6 months storage under stability test, amlodipine content of formulation I, II and $Norvasc^{(R)}$ tablet were $99.3{\pm}1.2%,\;98.9{\pm}1.4%\;and\;83.9{\pm}3.4%$, respectively. While amlodipine free base was unstable at the condition, its complex was not only significantly stable, but also similar in the dissolution pattern. These results suggest the usefulness of complex as a stable carrier for amlodipine free base.