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  • hydrophobic chromatography
    ¼Ò¼ö¼ºÅ©·Î¸¶Åä±×·¡ÇÇ
  • ion exchange chromatography
    À̿±³È¯Å©·Î¸¶Åä±×·¡ÇÇ
  • liquid chromatography
    ¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • paper chromatography
    ¿©°úÁöÅ©·Î¸¶Åä±×·¡ÇÇ
  • partition chromatography
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  • paper chromatography
    Á¾ÀÌÅ©·Î¸¶Åä±×·¡ÇÇ
  • partition chromatography
    ºÐ¹èÅ©·Î¸¶Åä±×·¡ÇÇ
  • thin-layer chromatography
    ¹ÚÃþÅ©·Î¸¶Åä±×·¡ÇÇ
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  • partition chromatography
    ºÐ¹è(ÝÂÛÕ)Å©·Î¸¶Åä±×·¡ÇÇ.
  • reverse phase liquid chromatography
    ¿ª»ó¾×üũ·Î¸¶Åä±×·¡ÇÇ
  • thin-layer chromatography
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  • age limit
    Á¤³â(ËøËç).
  • annual limit on intake (ALI)
    ¿¬°£Èí¼öÁ¦ÇÑ, ¿¬°£Èí¼öÇѵµ
  • audible limit
    °¡Ã»ÇѰè
  • check limit
    °¨»çÇѰè(ÊṴ̀˭).
  • confidence limit
    ½Å·ÚÇѰè(ÊṴ̀˭).
  • control limit
    °ü¸®ÇѰè(Ë´Ëö̰˭).
  • elastic limit
    ź¼ºÇѰè.
  • limit dextrin
    ÇѰ赦½ºÆ®¸°.
  • limit dextrinosis
    ÇѰ赦½ºÆ®¸°Áõ.
  • limit dose
    ÇѰ跮.
  • limit gauge
    ÇѰè°ÔÀÌÁö.
  • limit of error
    ¿ÀÂ÷ÇѰè(Ëí̤̰˭).
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  • dry column chromatography
    °ÇÁ¶¿øÅë(ËëðÏê­÷Ò) Å©·Î¸¶Åä±×·¡ÇÇ
  • dual-bed chromatography
    "ÀÌÁß»ó(ì£ñìßÉ) Å©·Î¸¶Åä±×·¡ÇÇ, (ÔÒ) coupled-layer chromatography"
  • elution chromatography
    ¿ë¸®(éÁ×î) Å©·Î¸¶Åä±×·¡ÇÇ
  • fast protein liquid chromatography
    °í¼Ó ´Ü¹éÁú ¾×ü(ÍÔáÜÓ±ÛÜòõäûô÷)Å©·Î¸¶Åä±×·¡ÇÇ
  • fast peptide liquid chromatography
    °í¼Ó(ÍÔáÜ) ÆéŸÀÌµå ¾×ü(äûô÷)Å©·Î¸¶Åä±×·¡ÇÇ
  • fast polynucleotide liquid chromatography
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  • filter paper chromatography
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  • flat-bed chromatography
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  • flip-flop chromatography
    ¾þħµÚħ Å©·Î¸¶Åä±×·¡ÇÇ
  • frontal chromatography
    ¾ÕºÎºÐ Å©·Î¸¶Åä±×·¡ÇÇ
  • gas chromatography
    °³½º Å©·Î¸¶Åä±×·¡ÇÇ
  • gas liquid chromatography
    °³½º ¾×ü(äûô÷) Å©·Î¸¶Åä±×·¡ÇÇ
  • gas solid chromatography
    °³½º °íü(ͳô÷) Å©·Î¸¶Åä±×·¡ÇÇ
  • gel chromatography
    Á© Å©·Î¸¶Åä±×·¡ÇÇ
  • gel filtration chromatography
    Á© ¿©°ú(ÕëΦ)Å©·Î¸¶Åä±×·¡ÇÇ
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GPC gastric parietal cell; gel permeation chromatography; giant papillary conjunctivitis; glycophorin C;...
GSC gas-solid chromatography; gravity settling culture
HPAC high-performance anion-exchange chromatography; hypothalamo-pituitary-adreno-cortical
HPLAC high-pressure liquid-affinity chromatography
HRC hereditary renal cancer; high-resolution chromatography; horse red cell; human rights committee
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LOQ Limit of quantitation
MRL Maximum Residue Limit
MDL method detection limit
OEL Occupational Exposure Limit
PEL Permissible Exposure Limit
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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 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)
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