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  • ¿µ¹®
    ÇѱÛ
  • molecular sieve
    ºÐÀÚü
  • standard sieve
    Ç¥ÁØÃ¼
  • sieve
    ü, Á¶¸®
  • sieve irradiation
    ¿©°úÁ¶»ç
  • affinity chromatography
    ģȭũ·Î¸¶Åä±×·¡ÇÇ
  • column chromatography
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  • chromatography
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  • gas-liquid chromatography
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  • gel-permeation chromatography
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  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
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  • high-pressure liquid chromatography
    °í¾Ð¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • hydrophobic chromatography
    ¼Ò¼ö¼ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • ion exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • liquid chromatography
    ¾×üũ·Î¸¶Åä±×·¡ÇÇ
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  • ¿µ¹®
    ÇѱÛ
  • chromatography
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  • sieve
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  • standard sieve
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  • molecular biology
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  • molecular
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  • molecular weight
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  • ¿µ¹®
    ÇѱÛ
  • molecular sieve
    ºÐÀÚü
  • sieve irradiation
    ¿©°úÁ¶»ç
  • sieve
    ü
  • standard sieve
    Ç¥ÁØÃ¼
  • affinity chromatography
    ģȭũ·Î¸¶Åä±×·¡ÇÇ
  • chromatography
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  • column chromatography
    ¿øÅëÅ©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
  • high-performance liquid chromatography
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  • high-pressure liquid chromatography
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  • hydrophobic chromatography
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  • ion exchange chromatography
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  • liquid chromatography
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  • paper chromatography
    Á¾ÀÌÅ©·Î¸¶Åä±×·¡ÇÇ
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  • ¿µ¹®
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  • High-molecular-weight kininogen
    °íºÐÀÚ·®Å°´Ï³ëÁø
  • genetics, molecular
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  • high molecular weight kinin
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  • high molecular weight kininogen
    °íºÐÀÚÁß·®Å°´Ï³ë°Õ
  • GLC= gas liquid chromatography
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • affinity chromatography
    ģȭ(öÑûú) Å©·Î¸¶Åä±×¶óÇÇ.
  • affinity chromatography
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  • anion exchange chromatography
    À½À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
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  • gas liquid chromatography =GLC
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  • gel-permeation chromatography
    °ÖÅõ°úÅ©·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
  • hydrophobic chromatography
    ¼Ò¼ö¼º Å©·Î¸¶Åä±×·¡ÇÇ
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  • ¿µ¹®
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  • molecular sieve
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  • sieve analysis
    üºÐ¼®(¡­ÝÂà°).
  • sieve bone =os ethmoidale
    »ç°ñ(ÞèÍé).
  • sieve graft
    ü»óÀ̽Ä(Æí)(¡­ßÒì¹ãÕø¸).
  • sieve irradiation
    ¿©°ú¹æ»ç¼±Á¶»ç
  • sieve therapy
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  • standard sieve
    Ç¥ÁØÃ¼(øöñÞô÷).
  • affinity chromatography
    ģȭ(öÑûú) Å©·Î¸¶Åä±×¶óÇÇ.
  • affinity chromatography
    ģȭ¼º Å©·Î¸¶Åä±×·¡ÇÇ
  • anion exchange chromatography
    À½À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • cation exchange chromatography
    ¾çÀ̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • chromatography
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  • column chromatography
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  • column chromatography
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  • gas chromatography
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  • ¿µ¹®
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  • Molecular layer
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  • Molecular layer [Plexiform layer]
    ºÐÀÚÃþ
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  • Band of molecular layer
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  • ¿µ¹®
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  • molecular parasitology
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  • ¿µ¹®
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  • molecular sieve chromatography
    ºÐÀÚ(ÝÂí­)ä Å©·Î¸¶Åä±×¶óÇÇ
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  • ¿µ¹®
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  • molecular sieve
    ºÐÀÚ(ÝÂí­)ä
  • molecular sieve coefficient
    ºÐÀÚ(ÝÂí­)ä °è¼ö(Ìõâ¦)
  • molecular-exclusion chromatography
    ºÐÀÚ¹èÀç(ÝÂí­ÛÉð¶) Å©·Î¸¶ÅäÅ©·¡ÇÇ
  • double-sieve mechanism
    ÀÌÁß(ì£ñì)°Å¸£±â ±âÀü(Ѧîú)
  • ribosomal sieve
    ¶óÀ̺¸¼ØÃ¼(ô÷)
  • average molecular weight
    Æò±ÕºÐÀÚ·® (øÁгÝÂí­Õá)
  • gram-molecular weight
    ±×·¥ ºÐÀÚ·®(ÝÂí­Õá)
  • minimum molecular weight
    ÃÖ¼ÒºÐÀÚ·®(õÌá³ÝÂí­Õá)
  • molecular activity
    ºÐÀÚȰ¼º(ÝÂí­üÀàõ)
  • molecular clock
    ºÐÀڽðè(ÝÂí­ãÁͪ)
  • molecular cloning
    ºÐÀÚ(ÝÂí­)Ŭ·Î´×
  • molecular disease
    ºÐÀÚº´(ÝÂí­Ü»)
  • molecular evolution
    ºÐÀÚÁøÈ­(ÝÂí­òäûù)
  • molecular genetics
    ºÐÀÚÀ¯ÀüÇÐ(ÝÂí­ë¶îîùÊ)
  • molecular hybrid
    ºÐÀÚ(ÝÂí­) Æ¢±â
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  • ¿µ¹®
    ÇѱÛ
  • molecular
    ºÐÀÚÀÇ
  • molecular biology
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  • molecular tumbling
    ºÐÀÚÅÒºí¸µ
  • molecular tumbling rate
    ºÐÀÚÅÒºí¸µÀ²
  • molecular weight
    ºÐÀÚ·®
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HPLC high-performance liquid chromatography; high-power liquid chromatography; high-pressure liquid chrom...
CCCC centrifugal countercurrent chromatography
FGC fibrinogen gel chromatography
FPLC fast protein liquid chromatography
GC ganglion cell; gas chromatography; general circulation; general closure; general condition; generali...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
RP-HPLC chromatography and reversed-phase high-performance liquid chromatography
MW 000-molecular weight
AMOVA Analyses of molecular variance
CoMFA Comparative Molecular Field Analysis
HMM High molecular mass
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • sieve graft
    »ç»ó À̽Ä
    ¿øÇüÀÇ ¾ÆÁÖ ÀÛÀº ¸î °³ÀÇ µµ°¡ Á¦°ÅµÈ ÇǺΠÀÌ½ÄÆí. ÀÌ´Â Å« ³ëÃâµÈ ºÎÀ§¸¦ µ¤´Âµ¥ »ç¿ëµÈ´Ù.
  • standard sieve
    Ç¥ÁØÃ¼
  • affinity chromatography
    ģȭ¼º Å©·Î¸¶Åä±×·¡ÇÇ
    ģȭ¼ºÀ» ÀÌ¿ëÇÏ¿© ƯÁ¤ ¹°ÁúÀ» ¿ë¾× ¼Ó¿¡¼­ ºÐ¸®ÇÏ´Â Å©·Î¸¶Åä±×·¡ÇÇ. Ç׿ø-Ç×ü, ±âÁú-È¿¼Ò, µ¶¼Ò-µ¶¼Ò°¡ °áÇÕÇÏ´Â ¼ö¿ëü, lectin-lectin °áÇÕ¼ö¿ëü µîÀÇ ÇÑÆíÀ» ºÒ¿ë¼ºÀÇ ´ãü¿¡ °øÀ¯°áÇÕ½Ã۰í À̰Ͱú ºÐ¸®ÇÏ°í ½ÍÀº ¿ë¾×À» ¹ÝÀÀ½ÃÄÑ Àß ¼¼Á¤Çϸé ģȭ¼ºÀÌ ³ôÀº ¹°Áú¸¸ÀÌ °áÇÕÇϹǷΠ½Å¼ÓÇÏ°Ô ¿øÇÏ´Â ¹°ÁúÀ» È¿À²ÀûÀ¸·Î ²ø¾î³¾ ¼ö ÀÖ´Ù.
  • anion exchange chromatography
    À½À̿ ±³È¯ Å©·Î¸¶Åä±×·¡ÇÇ
  • chromatography
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    È­ÇÐ ºÐ¼®ÀÇ ÇÑ ¹æ¹ý. ºÐ¼®µÇ´Â ¿ë¾×À» ÈíÂøÁ¦¸¦ ³Ö¾î ¼¼¿î À¯¸®°ü¿¡ ºÎÀ¸¸é °¢°¢ÀÇ ¿ë¾×Àº °íÁ¤»ó¿¡ ´ëÇÑ ÈíÂøµµ¿¡ µû¶ó¼­ ´Ù¸¥ ¼Óµµ·Î Åë°ú À̵¿ÇÏ¿©, ÈíÂø Ä®·³ÀÇ ´Ù¸¥ ³ôÀÌÀÇ »ö´ë¸¦ »ý¼ºÇÑ´Ù. ÀÌ ¸»Àº Ä®·³¿¡ »öÃþÀ» »ý¼ºÇÏÁö ¾Ê´Â °æ¿ì¿¡µµ, °°Àº ¿ø¸®¸¦ ÀÌ¿ëÇÏ´Â ´Ù¸¥ ¹æ¹ýµµ Æ÷ÇÔÇÏ¿© È®´ëÇØ¼­ »ç¿ëµÈ´Ù. Ä«¿Ã¸°, ¾Ë·ç¹Ì³ª, ½Ç¸®Ä«, Ȱ¼ºÅºÀÌ ÈíÂøÁ¦·Î¼­ »ç¿ëµÇ°í ÀÖ´Ù. Å©·Î¸¶Åä±×·¡ÇÇ´Â »ç¿ëµÇ´Â ÈíÂøÁ¦ÀÇ ¼ºÁú, °íÁ¤»óÀÇ ¹°¸®ÇÐÀû Ư¼º ȤÀº »ç¿ëµÇ´Â ¹æ¹ý µî¿¡ µû¶ó¼­ ºÐ·ùµÈ´Ù.
  • co-chromatography
    º¸Á¶ »öÃþ ºÐ¼®
  • column chromatography
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  • paper chromatography
    ÆäÀÌÆÛ Å©·Î¸¶Åä±×·¡ÇÇ
    ÈíÂø Ä®·³´ë½Å ÈíÃëÁö³ª º¸ÅëÀÇ ¿©°úÁö¸¦ »ç¿ëÇÏ´Â Å©·Î¸¶Åä±×·¡ÇÇ. °¢ ¼ººÐÀÌ °¢°¢ ´Ù¸¥ À̵¿ ¼Óµµ¿¡ ÀÇÇØ¼­ ºÐ¸®µÈ ÈÄ °¡½Ã Å©·Î¸¶Åä±×·¥ÀÌ ¸¸µé¾îÁø´Ù.
  • average molecular weight
    Æò±Õ ºÐÀÚ·®
  • cell adhesion molecular deficiency
    ¼¼Æ÷ À¯Âø ºÐÀÚ °áÇÌ
  • mean molecular weight
    Æò±Õ ºÐÀÚ·®
  • molecular
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  • molecular arrangement
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  • molecular biology
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  • molecular clock
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molecular sieve A gel-like material with pore sizes of such ranges as to exclude molecules above certain sizes; used in fractionating or purifying macromolecules.
(05 Mar 2000)
sieve 1. A utensil for separating the finer and coarser parts of a pulverized or granulated substance from each other. It consist of a vessel, usually shallow, with the bottom perforated, or made of hair, wire, or the like, woven in meshes. "In a sieve thrown and sifted."
2. A kind of coarse basket.
<botany> Sieve cells, cribriform cells. See Cribriform.
Origin: OE. Sive, AS. Sife; akin to D. Zeef, zift, OHG. Sib, G. Sieb. A. Cf. Sift.
Source: Websters Dictionary
(01 Mar 1998)
sieve bone A horizontal lamina from which are suspended the labyrinth, on either side, and the lamina perpendicularis in the centre; it fits into the ethmoidal notch of the frontal bone and supports the olfactory lobes of the cerebrum, being pierced with numerous openings for the passage of the olfactory nerves.
Synonym: lamina cribrosa ossis ethmoidalis, cribrum, sieve bone, sieve plate.
(05 Mar 2000)
sieve graft An obsolete term for a full-thickness skin graft taken after cutting multiple holes in it with a circular punch, thus leaving islands of skin in the donor area to heal it.
(05 Mar 2000)
sieve plate Perforated end walls separating the component cells (sieve elements) that make up the phloem sieve tubes in vascular plants. The perforations permit the flow of water and dissolved organic solutes along the tube and are lined with callose. The plates are readily blocked by further deposition of callose when the sieve tube is stressed or damaged.
(18 Nov 1997)
sieve tube The structure within the phloem of higher plants that is responsible for transporting organic material (sucrose, raffinose, amino acids, etc.) from the photosynthetic tissues (e.g. Leaves) to other parts of the plant. Made up of a column of cells (sieve elements) connected by sieve plates.
(18 Nov 1997)
absorption chromatography <investigation> Techniques for separating molecules based on differential absorption and elution. Term for separation methods involving flow of a fluid carrier over a nonmobile absorbing phase.
(18 Nov 1997)
adsorption chromatography Chromatography in which separation of substances is achieved by the difference in degree of adsorption of the compounds to a stationary phase.
(05 Mar 2000)
affinity chromatography <investigation> A technique of analytical chemistry used to separate and purify a biological molecule from a mixture, based on the attraction of the molecule of interest to a particular ligand which has been previously attached to a solid, inert substance.
The mixture is passed through a column containing the ligand attached to the stationary substance, so that the molecule of interest stays within the column while the rest of the mixture continues through to the end. Then, a different chemical is flushed through the column to detach the molecule from the ligand and bring it out separately from the rest of the mixture.
(09 Feb 1998)
gas chromatography <technique> A chromatographic technique (a type of column chromatography) in which the stationary phase is solid while the mobile phase is gaseous samples.
The gaseous samples are separated based on their different adsorption ability to the solid phase.
(09 Oct 1997)
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)
paper chromatography <technique> Separation method in which filter paper is used as the support.
A type of chromatography in which the stationary phase is a sheet of special-grade filter paper. It is in all other aspects similar to thin-layer chromatography.
Not a very sensitive method, but historically important as one of the first methods available for separating natural compounds.
(07 Mar 2000)
gel exclusion chromatography <investigation> A lab technique, a type of column chromatography, used to separate the components of a mixture by molecular size and to collect the molecules which are larger than a certain size. It is similar to gel filtration, small molecules are slowed or trapped by the pores in the gel beads filling the column, while large molecules, too large to fit into the pores, slide past the beads and get to the bottom of the column first. at this point, the large molecules are collected. Gel exclusion refers to the maximum size of molecule which will fit into the gel bead pores, and this lab technique is used to collect the molecules in the mixture which are larger than, or excluded from, the pores.
(09 Oct 1997)
gel filtration chromatography See: gel filtration.
(05 Mar 2000)
partition chromatography The separation of similar substances by repeated divisions between two immiscible liquids, so that the substances, in effect, cross the partition between the liquids in opposite directions; where one of the liquids is bound as a film on filter paper, the process is termed paper partition chromatography or paper chromatography.
(05 Mar 2000)
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  • molecular sieve chromatography - »õâ
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  • molecular film
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