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"liquid hybridization"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • colony hybridization
    Áý¶ôºÎÇÕÈ­
  • hybridization
    1. ±³Àâ 2. È¥¼ºÃ¼È­
  • hybridization plaque
    Çöóũȥ¼ºÃ¼È­
  • in situ hybridization
    Á¦ÀÚ¸®ºÎÇÕ¹ý, Á¦ÀÚ¸®±³Àâ(¹ý)
  • gas-liquid chromatography
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
    °í¼º´É¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • high-pressure liquid chromatography
    °í¾Ð¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • liquid
    1. ¾×ü, ¾×»ó 2. ¾×ü-
  • liquid air
    ¾×ü°ø±â
  • liquid calorimeter
    ¾×ü¿­·®°è
  • liquid chromatography
    ¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • liquid crystal
    ¾×Á¤
  • liquid glucose
    ¾×üÆ÷µµ´ç
  • liquid manometer
    ¾×ü¾Ð·Â°è
  • liquid nitrogen
    ¾×üÁú¼Ò
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hybridization
    ºÎÇÕÈ­
  • liquid
    ¾×ü, ¾×»ó
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • cell hybridization
    ¼¼Æ÷ºÎÇÕÈ­, ¼¼Æ÷ÇÏÀ̺긮µåÈ­
  • colony hybridization
    Áý¶ôºÎÇÕÈ­
  • hybridization colony
    Áý¶ôºÎÇÕÈ­
  • dot blot hybridization
    ¹ÝÁ¡Å¹º»ºÎÇÕ¹ý
  • fluorescent in-situ hybridization
    Çü±¤Á¦ÀÚ¸®ºÎÇÕ¹ý, Çü±¤µ¿¼Ò±³Àâ¹ý
  • hybridization
    ºÎÇÕÈ­
  • hybridization plaque
    ÇöóÅ©ºÎÇÕ¹ý
  • in situ hybridization
    Á¦ÀÚ¸®ºÎÇÕ¹ý
  • Northern hybridization
    ³ë´øºÎÇÕ¹ý
  • nucleic acid hybridization
    ÇÙ»êºÎÇÕÈ­
  • Southern hybridization
    ¼­´øºÎÇÕ¹ý
  • liquid air
    ¾×ü°ø±â
  • high-performance liquid chromatography
    °íÀÛÀ§¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • high-pressure liquid chromatography
    °í¾Ð·Â¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • liquid calorimeter
    ¾×ü¿­·®°è
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • GLC= gas liquid chromatography
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • air liquid interphase
    ±âü¾×ü°è¸é, ±â»ó¾×»ó°è¸é(ѨßÓäûßÓÍ£Øü)
  • gas liquid chromatography =GLC
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • high-performance liquid chromatography
    °íÀÛÀ§(íÂêÓ)¾×üũ·Î¸¶Åä±×¶óÇÇ
  • high-pressure liquid chromatography
    °í¾Ð·Â¾×ü Å©·Î¸¶Åä±×¶óÇÇ
  • hot liquid burn
    ¿­ÅÁ»ó(¿­ÅÁ»ó), °í¿Â¾×ü¿­»ó(°í¿Â¾×ü¿­»ó).
  • hot liquid burn
    ¿­ÅÁ»ó(Ëç̬Ë×), °í¿Â¾×ü¿­»ó(Ë­ËíËâ̧ËçË×).
  • hot liquid burn
    ¿­ÅÁ»ó(æð÷·ß¿), °í¿Â¾×ü¿­»ó(ÍÔè®äûô÷æðß¿).
  • ideal liquid
    ÀÌ»óÀ¯Ã¼(¡­êüô÷).
  • DNA-DNA hybridization
    DNA-DNA ¦Áö¿ì±â, DNA-DNA ºÎÇÕ°Ë»ç¹ý(ݬùê~)
  • DNA-RNA hybridization
    DNA-RNA ¦Áö¿ì±â, DNA-RNA ºÎÇÕ°Ë»ç¹ý(ݬùê~)
  • hybridization
    ºÎÇÕÈ­(ݬùêûù), ÀâÁ¾È­
  • hybridization
    ÇÏÀ̺긮µåÇü¼º, ÀâÁ¾Çü¼º(¡­û¡à÷), ±³Àâ(ÎßíÚ), ÀâÁ¾±³¹è, (DNAÀÇ) º¸ÇÕ°áÇÕ.
  • hybridization, DNA-DNA
    DNA-DNA ¦Áö¿ì±â, DNA-DNA ºÎÇÕÈ­(~ݬùêûù)
  • hybridization, DNA-RNA
    DNA-RNA ¦Áö¿ì±â, DNA-RNA ºÎÇÕÈ­(~ݬùêûù)
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • liquid liquid extraction
    ¾×ü-¾×üÃßÃâ.
  • liquid-liquid chromatography
    ¾×ü-¾×ü Å©·Î¸¶Åä±×·¡ÇÇ
  • cell hybridization
    ¼¼Æ÷ÇÏÀ̺긮µå Çü¼º (¡­û¡à÷)
  • colony hybridization
    Áý¶ôºÎÇÕÈ­(~ݬùêûù), ¼¼Æ÷±ººÎÇÕÈ­(~ݬùêûù)
  • fluorescence in situ hybridization
  • fluoroscent in-situ hybridization=FISH
    Çü±¤µ¿¼Ò±³Àâ¹ý
  • hybridization
    ÇÏÀ̺긮µåÇü¼º, ÀâÁ¾Çü¼º(¡­û¡à÷), ±³Àâ(ÎßíÚ), ÀâÁ¾±³¹è, (DNAÀÇ) º¸ÇÕ°áÇÕ.
  • hybridization
    ºÎÇÕÈ­(ݬùêûù), ÀâÁ¾È­
  • hybridization, DNA-DNA
    DNA-DNA ¦Áö¿ì±â, DNA-DNA ºÎÇÕÈ­(~ݬùêûù)
  • hybridization, DNA-RNA
    DNA-RNA ¦Áö¿ì±â, DNA-RNA ºÎÇÕÈ­(~ݬùêûù)
  • hybridization, Northern
    ³ë´øºÎÇÕ¹ý(ݬùêÛö)
  • hybridization, Southern
    ¼­´øºÎÇÕ¹ý(ݬùêÛö)
  • hybridization, colony
    Áý¶ôºÎÇÕÈ­(~ݬùêûù), ¼¼Æ÷±ººÎÇÕÈ­
  • hybridization, dot blot
    ¹ÝÁ¡Å¹º»ºÎÇÕ¹ý(~ݬùêÛö), ¹ÝÁ¡Ç¥Áö¹ý
  • hybridization, in situ
    Á¦ÀÚ¸®ºÎÇÕ¹ý(ݬùêÛö), µ¿¼ÒºÎÇÕ°áÇÕ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • liquid hybridization
    ¾×ü(äûô÷) Æ¢±â»ý¼º(ßæà÷)
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • liquid-liquid chromatography
    ¾×ü-¾×ü(äûô÷-äûô÷) Å©·Î¸¶Åä±×·¡ÇÇ
  • blot hybridization
    ºí·Ô Æ¢±âÇü¼º(û¡à÷)
  • cell hybridization
    ¼¼Æ÷(á¬øà) Æ¢±âÇü¼º(û¡à÷)
  • colony hybridization
    "ÄÝ·Î´Ï Æ¢±â Çü¼º(û¡à÷),"
  • cross-hybridization
    ±³Â÷(Îßó©)Æ¢±â Çü¼º(û¡à÷)
  • DNA-driven hybridization
    DNAÃßÁø(õÏòä) Æ¢±âÇü¼º(û¡à÷)
  • filter hybridization
    ¿©Áö(æ¤òµ) Æ¢±âÇü¼º
  • gel blot hybridization
    Á© ºí·Ô Æ¢±âÇü¼º(û¡à÷)
  • hybridization
    Æ¢±â»ý¼º(ßæà÷)
  • in situ hybridization
    Á¦ÀÚ¸® Æ¢±â »ý¼º(ßæà÷)
  • in situ hybridization assay
    Á¦ÀÚ¸® Æ¢±â»ý¼º(ßæà÷) ¾Æ½êÀÌ
  • RNA-driven hybridization
    RNA ÁÖµ¿(ñ«ÔÑ) ÇÏÀ̺긮µåÈ­(ûù)
  • saturation hybridization
    Æ÷È­(øéûù) Æ¢±â Çü¼º(û¡à÷)
  • solution hybridization
    ¿ë¾×(éÁäû) Æ¢±âÇü¼º(û¡à÷)
  • fast protein liquid chromatography
    °í¼Ó ´Ü¹éÁú ¾×ü(ÍÔáÜÓ±ÛÜòõäûô÷)Å©·Î¸¶Åä±×·¡ÇÇ
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • liquid
    ¾×ü, ¾×, ¾×üÀÇ, ¾×»óÀÇ
  • liquid diet
    À¯µ¿½Ä
  • liquid filled stomach method
    ¾×Ã¼Ãæ¸¸À§°Ë»ç¹ý
  • liquid helium
    ¾×È­Çï·ý
  • liquid image
    ¾×ü¿µ»ó
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
HPLC high-performance liquid chromatography; high-power liquid chromatography; high-pressure liquid chrom...
LLC Lewis lung carcinoma; liquid-liquid chromatography; long-leg cast; lymphocytic leukemia
LSC late systolic click; left side colon cancer; left subclavian; lichen simplex chronicus; liquid scint...
FISH Fluorescence In Situ Hybridization
CISH competitive in situ hybridization
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
LLE Liquid-liquid extraction
CGH Comparative genome hybridization
FISH Filter In Situ Hybridization
FISH Fluorescence In Situ Hybridization
GISH Genomic in situ hybridization
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cell hybridization
    ¼¼Æ÷ ÇÏÀ̺긮µå Çü¼º
  • abnormal liquid
    ºñÁ¤»ó ¾×ü
  • air liquid interphase
    ±âü ¾×ü °è¸é, ±â»ó ¾×»ó °è¸é
  • emulsion of liquid petrolatum
    À¯µ¿ ÆÄ¶óÇÉ ¿¡¸ÖÁ¯
  • liquid
    ¾×, ¿ë¾×, ¾×ü, ü¾×, ¾×»ó
    ÀÚ¿¬ »óÅ¿¡¼­ ¿ëÀÌÇÏ°Ô À¯µ¿ÇÏ´Â ¹°Áú.
  • liquid diet
    À¯µ¿½Ä
    °íÇü ¼ººÐÀÌ ¾øÀ¸¹Ç·Î ¾ÃÁö ¾Ê°í ±×´ë·Î »ïų ¼ö ÀÖ´Â À½½Ä¹°. ÀϹÝÀûÀ¸·Î ¼öºÐÀÌ ¸¹À¸¹Ç·Î Ä®·Î¸®¿øÀ¸·Î¼­ÀÇ °¡Ä¡´Â ÀûÀ¸¸ç, Á¦ÇÑµÈ ´Ü±â°£¿¡¸¸ ¾²ÀδÙ. °í¿­ÀÌ ³ª°í, ½Ä¿å ºÎÁøÀÏ ¶§¸¦ ºñ·ÔÇÏ¿© ¸ñÀ̳ª À̰¡ ¾ÆÇà ¶§, À§Àå ¼ö¼ú ÈÄ¿¡ ¾²ÀδÙ. º´ ÈÄ È¸º¹±â¿¡´Â ¼öÇÁ°¡ Àû´çÇϰí, ¼ÒÈ­ ±â´ÉÀÌ °¨ÅðµÇ¾úÀ» ¶§´Â Á×ÀÌ Àû´çÇÏ´Ù. ±× ¹Û¿¡ ¿ÀÆ®¹Ð, ¹°¿³, ¿ìÀ¯, ³­È², °úÁó, Å©¸², Á©¸®, û·®À½·á µîµµ º´¼¼¿¡ µû¶ó ¾²ÀδÙ.
  • liquid ferrous sulfate
    ¾×ü Ȳ»ê Á¦1ö
  • liquid form
    ¾×ü »óÅÂ
    ¹°À̳ª ±â¸§°ú °°ÀÌ ÀÚÀ¯·ÎÀÌ À¯µ¿ÇÏ¿© ¿ë±âÀÇ ¸ð¾ç¿¡ µû¶ó ±× ¸ð¾çÀÌ º¯Çϸç ÀÏÁ¤ÇÑ ÇüŸ¦ °¡ÁöÁö ¾Ê°í ¾ÐÃàÇØµµ °ÅÀÇ ºÎÇǰ¡ º¯ÇÏÁö ¾Ê´Â ¹°Áú. Á¤È®È÷´Â ¾×ü »óŶó°í ÇÑ´Ù. ¼ö¸¹Àº ¹°Áú °¡¿îµ¥ »ó¿Â, »ó¾Ð¿¡¼­ ÀÌ¿Í °°Àº »óŸ¦ °¡Áö´Â °ÍÀº ºñ±³Àû ÀûÀ¸³ª, Àû´çÇÑ ¿Âµµ¿Í ¾Ð·ÂÀÇ Á¶°ÇÀÌ °®Ãß¾îÁö¸é °ÅÀÇ ¸ðµç ¹°ÁúÀÌ ¾×ü·Î º¯ÇÒ ¼ö ÀÖÀ¸¸ç, ¹Ý´ë·Î ¾×üµµ ´Ù½Ã ±âü³ª °íü·Î º¯ÇÒ ¼ö ÀÖ´Ù. Áï, ¾×ü¶ó´Â °ÍÀº ¹°Áú¿¡ °íÀ¯ÇÑ ¼ºÁúÀÌ ¾Æ´Ï¶ó Á¶°Ç¿¡ µû¶ó¼­ ±âü·Îµµ °íü·Îµµ º¯ÇÒ ¼ö ÀÖ´Â ¹°ÁúÀÇ Á¸Àç »óÅÂÀÇ Çϳª¿¡ ºÒ°úÇÏ´Ù. ÀÌ·± ¶æ¿¡¼­ °íü»ó, ±âü»ó¿¡ ´ëÇØ¼­ ¾×ü»óÀ̶ó°í ÇÏ´Â °æ¿ìµµ ÀÖ´Ù. ¶ÇÇÑ ÇϳªÀÇ ¹°ÁúÀÌ °íü¿¡¼­ ¾×ü·Î º¯È­ÇÏ´Â Çö»óÀ» À¶ÇØ, ¾×ü¸é¿¡¼­ ±âÈ­ÇÏ´Â °ÍÀ» Áõ¹ßÀ̶ó°í Çϳª, ±âÈ­´Â ¾×ü ³»ºÎ¿¡¼­µµ ÀϾ¸ç, ¾×ü°¡ Àü¸éÀûÀ¸·Î ±âü·Î º¯ÇÏ´Â Çö»óÀ» ºñµîÀ̶ó°í ÇÑ´Ù. ÀÏÁ¤ÇÑ ¾Ð·ÂÇÏ¿¡¼­ÀÇ
  • liquid infant diet
    ¾×»ó À¯¾Æ½Ä
  • liquid paraffin
    À¯µ¿ ÆÄ¶óÇÉ
  • liquid scintillation counter
    ¾×ü ¼¶±¤ °è¼ö±â
  • marking liquid Ä¡Çü¿¡ ¹Ù¸¥ ÈÄ °ÇÁ¶µÇ¸é ÁÖÁ¶Ã¼¸¦ Ä¡Çü¿¡ ÀûÇÕ½ÃÄÑ ÁÖÁ¶Ã¼ ³»¸éÀÇ Á¶±â Á¢ÃËÁ¡À» ã´Â Àç·áÀÌ´Ù.

    marking medium

    ±³ÇÕÁö
    ÀÚ¿¬ Ä¡¾Æ¸¦ ¸ðÇü»ó¿¡¼­ »óÇÏ Ä¡¾Æ »çÀÌ¿¡ ³Ö°í ±³ÇÕ½ÃÄÑ Á¢Ã˰ü°è¸¦ °Ë»çÇÏ´Â ¸ÔÁö¿Í °°Àº °Í. µÎ²²°¡ ¾ã°í ±¤¹üÀ§ÇÏ°Ô ¹¯Áö ¾Ê´Â °ÍÀϼö·Ï ÁÁ´Ù. Á¤È­ÇÑ ±³ÇÕÀÇ ¼öÁý°ú ±³ÇÕ °£¼·À» Á¶Á¤Çϴµ¥ »ç¿ëµÈ´Ù.
  • milky liquid
    ¿ìÀ¯ °°Àº ¾×ü
  • powder-liquid method
    ºÐ, ¾×¹ý
  • wash liquid
    ¼¼¾×
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
liquid-liquid chromatography Chromatography in which both the moving phase and the stationary (or reverse-moving) phase are liquids, as in countercurrent distribution.
(05 Mar 2000)
cell hybridization Fusion of two or more dissimilar cells, leading to formation of a synkaryon.
(05 Mar 2000)
cross hybridization Annealing of a DNA probe to an imperfectly matching DNA molecule.
(05 Mar 2000)
protein hybridization The formation of a protein consisting of two or more polypeptide chains from separate and different polypeptide chains.
(12 Dec 1998)
hybridization <molecular biology> The process of joining two complementary strands of DNA or one each of DNA and RNA to form a double-stranded molecule.
Technique in which single stranded nucleic acids are allowed to interact so that complexes or hybrids, are formed by molecules with sufficiently similar, complementary sequences. By this means the degree of sequence identity can be assessed and specific sequences detected. The hybridisation can be carried out in solution or with one component immobilised on a gel or, most commonly, nitrocellulose paper.
Hybrids are detected by various means: visualisation in the electron microscope, by radioactively labelling one component and removing noncomplexed DNA or by washing or digestion with an enzyme that attacks single stranded nucleic acids and finally estimating the radioactivity bound. Hybridisations are done in all combinations: DNA DNA (DNA can be rendered single stranded by heat denaturation), DNA RNA or RNA RNA.
In situ hybridisations involve hybridising a labelled nucleic acid (often labelled with a fluorescent dye) to suitably prepared cells or histological sections. This is used particularly to look for specific transcription or localisation of genes to specific chromosomes (FISH analysis).
<zoology> The mating of individuals from different species or sub-species.
(13 Oct 1997)
somatic cell hybridization Production of a heterokaryon.
(05 Mar 2000)
nucleic acid hybridization Widely used technique which exploits the ability of complementary sequences in single-stranded dnas or rnas to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (kendrew, encyclopedia of molecular biology, 1994, p503; dorlands, 28th ed, p781)
(12 Dec 1998)
DNA hybridization A technique used to determine the relatedness of microorganisms by the speed and efficiency of the reassociation of single-stranded DNA to form double-stranded DNA when one of the strands originates from one organism and the other strand from another organism; occurs when the base sequences are complementary or nearly so.
(05 Mar 2000)
in situ hybridization <molecular biology> The use of a DNA or RNA probe to detect the complementary DNA sequence.
(12 Dec 1998)
in situ nucleic acid hybridization <molecular biology> The use of a DNA or RNA probe to detect the complementary DNA sequence.
(12 Dec 1998)
overlap hybridization A procedure to find and sequence a gene whose approximate position in a chromosome is known by classical genetic linkage studies. Starting with the known sequence of a gene shown by classical genetics to be near to the novel gene, new clones are picked from a genomic library by hybridisation with a short probe generated from the appropriate end of the known sequence. The new clones are then sequenced, new probes generated and the process repeated until the gene of interest is reached.
(18 Nov 1997)
fluorescence in situ hybridization <molecular biology, technique> A type of in situ hybridization in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy.
This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei.
Acronym: FISH
(25 Jun 1999)
fluorescent in situ hybridization See FISH.
(12 Dec 1998)
gas-liquid chromatography <technique> A chemistry lab technique, a type of column chromatography, used to separate the components of a mixed substance.
The substance is held stationary by an inert solid coated with an inert liquid which is not likely to evaporate (i.e. Is nonvolatile), while a gas (called an eluant) flows past it bringing out the components one at a time.
(09 Oct 1997)
chromatography, high pressure liquid Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
(12 Dec 1998)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 13 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hybridization
    ÀâÁ¾;È¥¼º
  • liquid
    ¾×ü
  • Condy's fluid(liquid)
    Äܵð¼Òµ¶¾×
  • Dutch liquid
    ¿°È­ ¿¡Æ¿·»
  • gas liquid chromatography
    =GAS CHROMATOGRATOGRAPHY
  • liquid
    ¾×ü(À¯µ¿Ã¼)ÀÇ;(ÀÛÀº »õ ¼Ò¸®,ÇÏ´Ã ºû µîÀÌ) ¸¼Àº;À¯Ã¢ÇÑ;À¯À½ÀÇ;(°øÃ¤ µî) µ·À¸·Î ¹Ù²Ü ¼ö ÀÖ´Â
  • liquid
    ¾×ü;À¯µ¿Ã¼;À¯À½
  • liquid air
    ¾×ü°ø±â
  • liquid fire
    ¾×È­(È­¿°¹æ»ç±â¿¡¼­ ¹ß»çµÇ´Â)
  • liquid fuel
    (·ÎÄÏÀÇ)¾×ü¿¬·Î
  • liquid measure
    ¾×·®
  • liquid sound
    À¯À½
  • semi liquid
    na;¹Ý ¾×ü(ÀÇ)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 1
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