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  • ¿µ¹®
    ÇѱÛ
  • paper chromatography
    ¿©°úÁöÅ©·Î¸¶Åä±×·¡ÇÇ
  • partition chromatography
    ºÐ¹èÅ©·Î¸¶Åä±×·¡ÇÇ
  • basal layer
    ¹Ù´ÚÃþ, ±âÀúÃþ
  • buffy layer
    ¿¬Ãþ
  • circular layer
    µ¹¸²Ãþ
  • clear layer
    Åõ¸íÃþ
  • compact layer
    Ä¡¹ÐÃþ
  • cone cell layer
    ¿ø»Ô¼¼Æ÷Ãþ, ¿øÃß¼¼Æ÷Ãþ
  • cortical layer
    °ÑÁúÃþ, ÇÇÁúÃþ
  • cuticular layer
    ²®ÁúÃþ
  • cavernous layer
    ÇØ¸éÃþ
  • cambium layer
    Çü¼ºÃþ
  • chondrogenic layer
    ¿¬°ñ¹ß»ýÃþ
  • choriocapillary layer
    ¸Æ¶ô¸·¸ð¼¼Ç÷°üÃþ
  • external pyramidal layer
    ¹Ù±ùÇǶó¹Ìµå¼¼Æ÷Ãþ, ¿ÜÃøÃßü¼¼Æ÷Ãþ
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  • ¿µ¹®
    ÇѱÛ
  • partition chromatography
    ºÐ¹èÅ©·Î¸¶Åä±×·¡ÇÇ
  • agar layer method
    ¿ì¹«ÁßÃþ¹ý
  • basal layer
    ¹Ù´ÚÃþ
  • buffy layer
    ¿¬Ãþ
  • cavernous layer
    ÇØ¸éÃþ
  • chondrogenic layer
    ¿¬°ñ¹ß»ýÃþ
  • choriocapillary layer
    ¸Æ¶ô¸·¸ð¼¼Ç÷°üÃþ
  • circular layer
    µ¹¸²Ãþ
  • clear layer
    Åõ¸íÃþ
  • compact layer
    Ä¡¹ÐÃþ
  • cone cell layer
    ¿ø»Ô¼¼Æ÷Ãþ
  • cortical layer
    °ÑÁúÃþ
  • cuticular layer
    ²®ÁúÃþ
  • ependymal layer
    ³ú½Ç¸·Ãþ
  • external pyramidal layer
    ¹Ù±ùÇǶó¹Ô¼¼Æ÷Ãþ, ¹Ù±ùÇǶó¹ÔÃþ
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  • ¿µ¹®
    ÇѱÛ
  • Henle s layer
    Çî·¹Ãþ.
  • Henle s layer
    Çî·¹Ãþ
  • Henles fiber layer
    Çî·¹½Å°æ¼¶À¯Ãþ
  • Huxley s layer
    Çä½½¸®Ãþ.
  • Huxley s layer
    Çä½½¸®Ãþ
  • Huxleys layer
    Çä½½¸®Ãþ
  • Langhans layer
    ¶û±×ÇѽºÃþ.
  • Malpighian layer
    ¸»ÇDZâÃþ
  • Nitabuchs layer
    ´ÏŸºÎÈåÃæ.
  • Sattlers layer
    ÀÚÆ²·¯Ãþ
  • adipose layer
    Áö¹æÃþ(ò·Û¸öµ)
  • adipose layer
    Áö¹æÃþ
  • agar layer method
    ÇÑõÁßÃþ¹ý(¡­ñìöµÛö).
  • anterior layer
    ¾ÕÃþ
  • arrangement of germinal layer
    Á¾ÀÚÃþ¹è¿­
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  • ¿µ¹®
    ÇѱÛ
  • anion exchange chromatography
    À½À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • cation exchange chromatography
    ¾çÀ̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • chromatography
    Âø»öÁ¶¿µ¼ú
  • column chromatography
    Ä®·³ Å©·Î¸¶Åä±×¶óÇÇ
  • column chromatography
    ¿øÅë Å©·Î¸¶Åä±×·¡ÇÇ.
  • gas chromatography
    °¡½ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • gas liquid chromatography =GLC
    °¡½º¾×üũ·Î¸¶Åä±×·¡ÇÇ.
  • 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
  • ion exchange chromatography
    À̿±³È¯Å© ·Î¸¶Åä±×·¡ÇÇ.
  • ion-exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • liquid chromatography
    ¾×üũ·Î¹ÌÅä±×·¡ÇÇ
  • liquid-liquid chromatography
    ¾×ü-¾×ü Å©·Î¸¶Åä±×·¡ÇÇ
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  • ¿µ¹®
    ÇѱÛ
  • Muscle layer
    ±ÙÀ°Ãþ
    [¿¾ ¿ë¾î] ±ÙÃþ
  • Muscular layer
    ±ÙÀ°Ãþ
    [¿¾ ¿ë¾î] ±ÙÃþ
  • Myoelastic layer
    ±ÙÀ°Åº·ÂÃþ
    [¿¾ ¿ë¾î] ±Ùź·ÂÃþ
  • Pretracheal layer
    ±â°ü¾ÕÃþ
    [¿¾ ¿ë¾î] ±â°üÀü¿±
  • Deep layer
    ±íÀºÃþ
    [¿¾ ¿ë¾î] ½É´ë
  • Deep layer
    ±íÀºÃþ
    [¿¾ ¿ë¾î] ½É¿±
  • Visceral layer [Epicardium]
    ³»ÀåÂÊÃþ [½ÉÀå¹Ù±ù¸·]
    [¿¾ ¿ë¾î] ÀåÃøÆÇ(½É¿Ü¸·)
  • Subendothelial layer
    ³»ÇǹØÃþ
    [¿¾ ¿ë¾î] ³»ÇÇÇÏÃþ
  • Ependymal layer
    ³ú½Ç¸·Ãþ
    [¿¾ ¿ë¾î] »óÀÇÃþ
  • Circular muscle layer
    µ¹¸²±ÙÀ°Ãþ
    [¿¾ ¿ë¾î] À±ÁÖ±ÙÃþ
  • Circular layer
    µ¹¸²Ãþ
    [¿¾ ¿ë¾î] À±ÁÖ±ÙÃþ
  • Circular layer
    µ¹¸²Ãþ
    [¿¾ ¿ë¾î] À±ÁÖÃþ
  • Posterior layer
    µÚÃþ
    [¿¾ ¿ë¾î] ÈÄ¿±
  • Supravascular layer
    ¸Æ°üÀ§Ãþ
    [¿¾ ¿ë¾î] ¸Æ°ü»óÃþ
  • Vascular layer
    ¸Æ°üÃþ
    [¿¾ ¿ë¾î] ¸Æ°üÃþ
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  • ¿µ¹®
    ÇѱÛ
  • germ layer
    ¹è¿±(ÛÏç¨)
  • gradient layer
    ±¸¹èÃþ(ÎþÛÕöµ)
  • half-value layer
    ¹Ý°¨Ãþ(ÚâÊõöµ)
  • Helmholtz double layer
    Ç︧ȦÃ÷ ÀÌÁßÃþ(ì£ñìöµ)
  • layer line
    Ãþ¼±(öµàÊ)
  • monomolecular layer
    ´ÜºÐÀÚÃþ(Ó¤ÝÂí­öµ)
  • thin-layer electrophoresis
    ¹ÚÃþ Àü±â¿µµ¿(ÚÝöµï³Ñ¨ç¶ÔÑ)
  • thin-layer gel filtration
    ¹ÚÃþ(ÚÝöµ) Á©¿©°ú(ÕëΦ)
  • adsorption chromatography
    ÈíÂø(ýåó·)Å©·Î¸¶Åä±×·¡ÇÇ
  • affinity chromatography
    ģȭ(öÑûú)Å©·Î¸¶Åä±×·¡ÇÇ
  • argentation chromatography
    ÀºÈ­(ëÞûù) Å©·Î¸¶Åä±×·¡ÇÇ
  • ascending chromatography
    »óÇà(ß¾ú¼)Å©·Î¸¶Åä±×·¡ÇÇ
  • carrier displacement chromatography
    ij¸®¾î ġȯ(öÇüµ) Å©·Î¸¶Åä±×·¡ÇÇ
  • centrifugal partition chromatography
    ¿ø½ÉºÐ¹è(êÀãýÝÂÛÕ) Å©·Î¸¶Åä±×·¡ÇÇ
  • chromatography
    Å©·Î¸¶Åä±×·¡ÇÇ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
Rst in paper or thin layer chromatography, the distance that a spot of a substance has moved, relative t...
TLC tender loving care; thin-layer chromatography; total L-chain concentration; total lung capacity; tot...
ECG Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ
   = EKG
  1. Conducting System Structu...
CAP camptodactyly-arthropathy-pericarditis [syndrome]; Canada Assistance Plan; capsule; captopril; catab...
CCD calibration curve data; central core disease; charge-coupled device; childhood celiac disease; cleid...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CCD Charge Coupled Device
GPCR G Protein-Coupled Receptor
GRK G protein coupled receptor kinase
GCR G protein-coupled receptor
GPR G protein-coupled receptor
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cellular proliferative layer
    ¼¼Æ÷¼º Áõ½ÄÃþ
    ¼¼Æ÷ÀÇ µ¿ÀÏÇüÅÂÀÇ Àç»ý»ê ¶Ç´Â Áõ½ÄÃþ.
  • choroid layer
    ¸Æ¶ô¸· Ãþ
    Ç÷°üÀ» °¡Áø ¾È±¸ÀÇ Ãþ.
  • compact layer
    Ä¡¹Ð Ãþ
  • double layer
    ÀÌÁß Ãþ
  • double layer fluorescent antibody technique
    ÀÌÃþ Çü±¤ Ç×ü¹ý
  • floegel's layer
    ÇÃ·Ú°Ö Ãþ
    ±Ù ¼¶À¯ÀÇ Åõ¸í ¿Ü°ü¿¡ ÀÖ´Â °ú¸³ Ãþ.
  • interface layer
    °è¸éÃþ
  • layer
    Ãþ
    ½×Àº, °ãÄ£, Ä¥ÇÑ, µÎ²².
  • malpighian layer
    malpighi Ãþ
  • mantle layer
    ¿ÜÅõ Ãþ
  • molecular layer
    ºÐÀÚ Ãþ
  • mucous layer
    Á¡¾×Ãþ
  • nerve cell layer
    ½Å°æ ¼¼Æ÷ Ãþ
  • odondoblastic layer
    Á¶»ó¾Æ¼¼Æ÷ Ãþ
  • odontoblastic layer
    Á¶»ó¾Æ¼¼Æ÷Ãþ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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)
reversed phase chromatography A form of partitionary chromatography in which the stationary phase is more polar than the mobile phase.
(05 Mar 2000)
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)
chromatography, affinity A chromatographic technique that utilises the ability of biological molecules to bind to certain ligands specifically and reversibly. It is used in protein biochemistry.
(12 Dec 1998)
chromatography, agarose A method of gel filtration chromatography using agarose, the non-ionic component of agar, for the separation of compounds with molecular weights up to several million.
(12 Dec 1998)
chromatography, deae-cellulose A type of ion exchange chromatography using diethylaminoethyl cellulose (deae-cellulose) as a positively charged resin.
(12 Dec 1998)
chromatography, gas Fractionation of a vaporised sample as a consequence of partition between a mobile gaseous phase and a stationary phase held in a column. Two types are gas-solid chromatography, where the fixed phase is a solid, and gas-liquid, in which the stationary phase is a nonvolatile liquid supported on an inert solid matrix.
(12 Dec 1998)
chromatography, gel Chromatography on non-ionic gels without regard to the mechanism of solute discrimination.
(12 Dec 1998)
chromatography, high pressure liquid Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
(12 Dec 1998)
chromatography, ion exchange Separation technique in which the stationary phase consists of ion exchange resins. The resins contain loosely held small ions that easily exchange places with other small ions of like charge present in solutions washed over the resins.
(12 Dec 1998)
chromatography, liquid Chromatographic techniques in which the mobile phase is a liquid.
(12 Dec 1998)
chromatography paper Used in paper chromatography.
Synonym: high quality filter paper.
Congo red paper, paper impregnated with Congo red; used as a pH indicator, changing from blue-violet at 3.0 to red at 5.0.
Filter paper, an unsized paper used in pharmacy and chemistry for filtering solutions; many varieties are used for paper chromatography.
(05 Mar 2000)
column chromatography A form of partition, adsorption, ion exchange, or affinity chromatography in which one phase is liquid (aqueous) flowing down a column packed with the second phase, a solid; the dissolved substances form a partition between the solid and liquid phases depending on the chemical and physical conditions of each phase; the more strongly adsorbed solutes reach the bottom of the column later than the less strongly adsorbed ones.
(05 Mar 2000)
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    ³õ´Â »ç¶÷;Ãþ
  • layer cake
    ÄÑ »çÀÌ¿¡ Å©¸² µûÀ§¸¦ ³ÖÀº °úÀÚ
  • mine layer
    ±â·Ú ºÎ¼³ÇÔ
  • nepheloid layer
    (Á¡Åä ±¸¼º¹° Å©±âÀÇ ¹Ì¼¼ÇÑ ±¤¹°ÀÌ ¶°´Ù´Ï´Â ½ÉÇØÀÇ)ÇöŹÃþ
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