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"fast protein liquid chromatography"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • Bence Jones protein
    º¥½º-Á¸½º´Ü¹éÁú
  • coat protein
    ¿ÜÇǴܹéÁú
  • competitive protein binding radioassay
    °æÇմܹéÁú°áÇÕ¹æ»çÃøÁ¤(¹ý)
  • conjugated protein
    Á¢ÇմܹéÁú, °áÇմܹéÁú
  • contractile protein
    ¼öÃà´Ü¹éÁú
  • core protein
    ÇٽɴܹéÁú
  • C-reactive protein
    C-¹ÝÀÀ´Ü¹éÁú
  • cytotoxic cell protein
    ¼¼Æ÷µ¶¼º¼¼Æ÷´Ü¹éÁú
  • carrier protein
    ¿î¹Ý´Ü¹éÁú
  • catabolite (gene) activator protein
    ºÐÇØ´ë»ç»ê¹°(À¯ÀüÀÚ)Ȱ¼º´Ü¹éÁú
  • catabolite activator protein
    ºÐÇØ´ë»ç»ê¹°È°¼º´Ü¹éÁú
  • denatured protein
    º¯¼º´Ü¹éÁú
  • derived protein
    À¯µµ´Ü¹éÁú
  • different membrane protein
    À¯°ü¸·´Ü¹éÁú
  • extracellular matrix protein
    ¼¼Æ÷¹Ù±ù¹ÙÅÁÁú´Ü¹éÁú, ¼¼Æ÷¿Ü±âÁú´Ü¹éÁú
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  • ¿µ¹®
    ÇѱÛ
  • carrier protein
    ¿î¹Ý´Ü¹é, ¿î¹Ý´Ü¹éÁú
  • catabolite activating protein
    ÀÌÈ­»ê¹°È°¼ºÈ­´Ü¹é
  • coat protein
    ¿ÜÇǴܹé
  • competitive protein binding radioassay
    °æÇմܹé°áÇÕ¹æ»çÃøÁ¤(¹ý)
  • conjugated protein
    º¹Çմܹé, Á¢ÇմܹéÁú
  • contractile protein
    ¼öÃà´Ü¹éÁú
  • core protein
    Çٽɴܹé
  • cytotoxic cell protein
    ¼¼Æ÷µ¶¼º¼¼Æ÷´Ü¹é
  • denatured protein
    º¯¼º´Ü¹é
  • deposit protein
    ÀúÀå´Ü¹éÁú
  • derived protein
    À¯µµ´Ü¹éÁú
  • different membrane protein
    À¯°ü¸·´Ü¹é
  • endogenous protein
    ³»ÀδܹéÁú
  • extracellular matrix protein
    ¼¼Æ÷¿Ü°£Áú´Ü¹é
  • protein-losing enteropathy
    ´Ü¹é¼Ò½ÇâÀÚº´Áõ
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  • ¿µ¹®
    ÇѱÛ
  • Integral membrane protein
    ÅëÇÕ(÷Öùê) ¸·´Ü¹é(Ø­Ó±ÛÜ)
  • M protein
    M´Ü¹éÁú
  • M protein
    M´Ü¹é.
  • NPN= non protein nitrogen
    ºñ´Ü¹éÁú¼Ò.
  • POMP (principal outer membrane protein)
    ÁÖ¿ä¿Ü¸·´Ü¹éÁú
  • PPD (purified protein derivatives)
    ÇÇÇǵð, Á¤Á¦´Ü¹éÁú·ù(À¯µµÃ¼)
  • PPD(Purified protein derivative) test
    PPD °Ë»ç.
  • Reiters protein
    ¶óÀÌÅÍ ¸Åµ¶Áø´Ü¿ë´Ü¹éÁú
  • S100 protein
    S100 ´Ü¹éÁú
  • actin-binding protein
    ¾×ƾ °áÇմܹé(¡­Ì¿ùêÓ±ÛÜ)
  • activated protein C inhibitor
    Ȱ¼ºÈ­´Ü¹éÁú C ¾ïÁ¦Á¦
  • activated protein C resistance
    Ȱ¼ºÈ­C´Ü¹é³»¼º
  • acute phase protein
    ±Þ¼ºº´±â´Ü¹éÁú
  • acute phase reactive protein
    ±Þ¼º±â ¹ÝÀÀ¼º ´Ü¹é.
  • amyloid precurssor protein
    ¾Æ¹Ð·ÎÀ̵å Àü±¸ ´Ü¹éÁú
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  • ¿µ¹®
    ÇѱÛ
  • fast multiplanar spoiled gradient recalled sequence
    °í¼Ó ´Ù¸é ȸ¼Õ °æ»ç ȸº¹ ¿¬¼â
  • fast neutron
    ¼ÓÁß¼ºÀÚ
  • fast scan
    °í¼Ó ½ºÄµ
  • fast scan
    °í¼Ó (ÍÔáÜ) ½ºÄµ
  • fast scan effect
    °í¼Ó ½ºÄµ È¿°ú
  • fast scan imaging
    °í¼Ó ½ºÄµ ¿µ»ó
  • fast spin echo (FSE)
    °í¼Ó ½ºÇÉ ¿¡ÄÚ
  • fast spin echo imaging
    °í¼Ó ½ºÇÉ ¿¡ÄÚ ¿µ»ó
  • fast time constant circuit
    °í¼Ó ½Ã°£ °íÁ¤ ȸ·Î
  • fast time constant circuit
    °í¼Ó½Ã°£ °íÁ¤È¸·Î (ÍÔáÜãÁÊà ͳïÒüÞÖØ)
  • nuclear fast red
    ÇÙ³»¼º Àû»ö¼Ò(ú·Ò±àõîåßä áÈ).
  • ultra fast sequence
    Ãʰí¼Ó ¿¬¼â
  • air liquid interphase
    ±âü¾×ü°è¸é, ±â»ó¾×»ó°è¸é(ѨßÓäûßÓÍ£Øü)
  • emulsion of liquid petrolatum
    À¯µ¿(êüÔÑ)ÆÄ¶óÇÉ¿¡¸ÖÁ¯.
  • extracellular liquid volume
    ¼¼Æ÷¿Ü¾×·®(¡­äûåÖ).
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  • ¿µ¹®
    ÇѱÛ
  • filter paper chromatography
    ¿©Áö(Õëòµ) Å©·Î¸¶Åä±×·¡ÇÇ
  • flat-bed chromatography
    Æò»ó(øÁßÉ) Å©·Î¸¶Åä±×·¡ÇÇ
  • flip-flop chromatography
    ¾þħµÚħ Å©·Î¸¶Åä±×·¡ÇÇ
  • frontal chromatography
    ¾ÕºÎºÐ Å©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °³½º Å©·Î¸¶Åä±×·¡ÇÇ
  • gas solid chromatography
    °³½º °íü(ͳô÷) Å©·Î¸¶Åä±×·¡ÇÇ
  • gel chromatography
    Á© Å©·Î¸¶Åä±×·¡ÇÇ
  • gel exclusion chromatography
    Á© ¹èÁ¦(ÛÉð¶)Å©·Î¸¶Åä±×·¡ÇÇ
  • gel filtration chromatography
    Á© ¿©°ú(ÕëΦ)Å©·Î¸¶Åä±×·¡ÇÇ
  • gel permeation chromatography
    Á© Åõ°ú(÷âΦ) Å©·Î¸¶Åä±×·¡ÇÇ
  • gradient sievorptive chromatography
    ±¸¹è ¿©°úÈíÂø(ÎþÛÕÕëΦýåó·) Å©·Î¸¶Åä±×·¡ÇÇ
  • hydrophobic chromatography
    ¼Ò¼ö(áÂâ©) Å©·Î¸¶Åä±×·¡ÇÇ
  • hydrophobic interaction chromatography
    ¼Ò¼ö »óÈ£ÀÛ¿ë(áÂâ©ßÓû»íÂéÄ) Å©·Î¸¶Åä±×·¡ÇÇ
  • intervent dilution chromatography
    °³ÀÔÈñ¼®(Ë¿ìýýüà·) Å©·Î¸¶Åä±×·¡ÇÇ
  • ion chromatography
    À̿ ũ·Î¸¶Åä±×·¡ÇÇ
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PSMF protein-sparing modified fast
ABP actin-binding protein; ambulatory blood pressure; American Board of Pedodontics; American Board of P...
CBP calcium-binding protein; carbohydrate-binding protein; cardiopulmonary bypass; chlorobiphenyl; cobal...
CP candle power; capillary pressure; cardiac pacing; cardiac performance; cardiopulmonary; caudate puta...
CRP chronic relapsing pancreatitis; corneal-retinal potential; coronary rehabilitation program; C-reacti...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
HPLC-ED High-performance liquid chromatography with electrochemical detection
HPLC-ESI-MS High-performance liquid chromatography-electrospray ionization-mass spectrometry
HPLC-MS High-performance liquid chromatography-mass spectrometry
LC Liquid Chromatography
LCEC Liquid chromatography with electrochemical detection
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cellular retinoid acid-binding protein
    ¼¼Æ÷³» ·¹Æ¼³ëÀ̵å»ê °áÇÕ ´Ü¹é
  • chromatographic protein separation
    Å©·Î¸¶Åä±×·¡Çǹý ´Ü¹é ºÐ¸®
  • D-myeloma protein
    D-°ñ¼öÁ¾ ´Ü¹é
    ¸é¿ª ±Û·ÎºÎ¸°ÀÇ ÇÑ ºÎ·ùÀÎ IgD¸¦ »ý»êÇÏ´Â °ñ¼öÁ¾¿¡¼­ ¸¸µé¾îÁø ´Ü¹éÁú.
  • eosinophil protein X
    È£»ê±¸ ´Ü¹é X
  • estrogen receptor protein
    ¿¡½ºÆ®·Î°Õ ¼ö¿ëü ´Ü¹éÁú
  • hapten-protein conjugate
    ÇÕÅÙ ´Ü¹é °áÇÕ¹°
  • heat-aggregated protein
    ¿­ ÀÀÁý ´Ü¹é
  • hepatic protein
    °£ ´Ü¹é, °£ ´Ü¹éÁú
    °£ÀÇ ´Ü¹éÁú.
  • high protein diet
    °í´Ü¹é ½ÄÀÌ
  • membrane protein
    ¸· ´Ü¹éÁú
  • myotonin-protein kinase
    ¹Ì¿ÀÅä´Ñ-´Ü¹é Ű³ªÁ¦
  • pathologic plasma protein
    º´Àû Ç÷Àå ´Ü¹é
  • penicillin binding protein
    Æä´Ï½Ç¸° °áÇÕ ´Ü¹éÁú
  • perturbation of protein
    ´Ü¹éÁú º¯ÅÂ
  • plasma protein
    Ç÷Àå ´Ü¹é, Ç÷Àå ´Ü¹éÁú
    1. Ç÷Àå¿¡ Á¸ÀçÇÏ´Â ¿©·¯ Á¾·ùÀÇ ´Ü¹éÁú. ¿î¹Ý ´Ü¹éÁú
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
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)
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)
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, 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 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)
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