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"gel layer"¿¡ ´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
  • 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
  • embryonic layer
    ¹è¾ÆÃþ
  • ependymal layer
    ³ú½Ç¸·Ãþ
  • feeder layer
    ¿µ¾ç¼¼Æ÷Ãþ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • 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
  • thin-layer chromatography
    ¹ÚÃþÅ©·Î¸¶Åä±×·¡ÇÇ
  • ependymal layer
    ³ú½Ç¸·Ãþ
  • external pyramidal layer
    ¹Ù±ùÇǶó¹Ô¼¼Æ÷Ãþ, ¹Ù±ùÇǶó¹ÔÃþ
  • feeder layer
    ¿µ¾ç¼¼Æ÷Ãþ
  • fibrous layer
    ¼¶À¯ÆÇ, ¼¶À¯Ãþ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • gel filtration
    Á©¿©°ú(¹ý).
  • gel filtration
    °Ö¿©°ú(¹ý)
  • gel test
    °Ö½ÃÇè.
  • gel-permeation
    °ÖÅõ°ú
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
  • inelastic gel
    ºñź·Â¼º(Þª÷¥æ³àõ) °Ö.
  • polyacrylamide gel
    Æú¸®¾ÆÅ©¸±¾Æ¹Ìµå°Ö
  • pulsed-field gel electrophoresis (PFGE)
    °£Çæ¾ß Àü±â¿µµ¿
  • Bowmans layer
    º¸¿ì¸¸Ãþ
  • Chievitz layer
    ½¬ºñÃ÷Ãþ
  • Hallers layer
    ÇÒ·¯Ãþ
  • Haxley s layer
    Çн½¸®Ãþ.
  • Henle s layer
    Çî·¹Ãþ.
  • Henle s layer
    Çî·¹Ãþ
  • Henles fiber layer
    Çî·¹½Å°æ¼¶À¯Ãþ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • crystalline gel
    °áÁ¤°Ö.
  • electrophoresis, gel
    Á©Àü±â¿µµ¿
  • electrophoresis, polyacrylamide gel
    Æú¸®¾ÆÅ©¸±¾Æ¸¶À̵åÁ©Àü±â¿µµ¿
  • electrophoresis, slab gel
    Æò¸éÁ©Àü±â¿µµ¿
  • gel
    Á©, ±³È­Ã¼(Îïûùô÷).
  • gel
    °Ö
  • gel diffusion
    ÇÑõȮ»ê
  • gel diffusion precipitin reaction
    ÇÑõȮ»ê ħ°­¹ÝÀÀ
  • gel diffusion test, quantitative
    ÇÑõȮ»ê Á¤·®¹ý
  • gel elasticity
    °Öź¼º.
  • gel filtration
    Á©¿©°ú(¹ý).
  • gel filtration
    °Ö¿©°ú(¹ý)
  • gel test
    °Ö½ÃÇè.
  • gel-permeation
    °ÖÅõ°ú
  • gel-permeation chromatography
    °ÖÅõ°úÅ©·Î¸¶Åä±×·¡ÇÇ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿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
  • agar gel electrophoresis
    ÇÑõ(ùÎô¸)Á©Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • calcium phosphate gel
    Àλê(×òß«)Ä®½· Á©
  • disc gel electrophoresis
    ºÒ¿¬¼Ó(ÝÕææáÙ) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • field inversion gel electrophoresis
    ÀåÀüµµ(íÞï´Óî) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • gel
    Á©
  • gel blot hybridization
    Á© ºí·Ô Æ¢±âÇü¼º(û¡à÷)
  • gel chromatography
    Á© Å©·Î¸¶Åä±×·¡ÇÇ
  • gel diffusion
    Á© È®»ê(üªß¤)
  • gel electrofocusing
    Á© Àü±â(ï³Ñ¨)Æ÷Ä¿½Ì
  • gel exclusion chromatography
    Á© ¹èÁ¦(ÛÉð¶)Å©·Î¸¶Åä±×·¡ÇÇ
  • gel filtration chromatography
    Á© ¿©°ú(ÕëΦ)Å©·Î¸¶Åä±×·¡ÇÇ
  • gel immunofiltration
    Á© ¸é¿ª¿©°ú(Øóæ¹ÕëΦ)
  • gel osmometer
    Á© »ïÅõ°è(ß¶÷âͪ)
  • gel permeation chromatography
    Á© Åõ°ú(÷âΦ) Å©·Î¸¶Åä±×·¡ÇÇ
  • gradient gel electrophoresis
    ±¸¹è(ÎþÛÕ) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
H1/2 half-value layer
HVL, hvl half-value layer
IPL inner plexiform layer; intrapleural
ITLC instant thin-layer chromatography
LFL left frontolateral; leukocyte feeder layer; lower flammable limit
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
NFL Nerve fiber layer
RNFL Retinal Nerve Fiber Layer
RNFL Retinal nerve fibre layer
SGL Superficial gray layer
TLC Thin Layer Chromatography
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cellular layer
    ¼¼Æ÷ Ãþ
    ¼¼Æ÷°¡ °ÅÀÇ ÀÏÁ¤ÇÑ µÎ²²ÀÇ, ȬÀ̺Ҹð¾çÀÇ Á¶Á÷ ±¸Á¶¸¦ °¡Áö´Â °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
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
gel retardation assay A lab technique used to find out if there are proteins binding a fragment of DNA (in a DNA-protein complex) by watching how fast the DNA fragment moves through an electric field and seeing whether it moves slower when a particular protein is also present.
(09 Oct 1997)
gel structure Brush heap structure of fibrils giving firmness to hydrocolloids.
(05 Mar 2000)
gel transfer Any lab technique used to transfer substances which had been separated using gel electrophoresis from the gel to a membrane for further processing or analysis. For example: any type of blotting.
(09 Oct 1997)
pharmacopeial gel A suspension, in a water medium, of an insoluble drug in hydrated form wherein the particle size approaches or attains colloidal dimensions.
(05 Mar 2000)
chromatography, gel Chromatography on non-ionic gels without regard to the mechanism of solute discrimination.
(12 Dec 1998)
colloidal gel A colloid that has developed resistance to flow because of chemical or thermal change.
(05 Mar 2000)
polyacrilamide gel A white, water-soluble, solid gel used as a gel base for electrophoresisand as a thickening or adhesive additive in other industrialapplications.
(09 Oct 1997)
polyacrylamide gel electrophoresis Analytical and separative technique in which molecules, particularly proteins, are separated by their different electrophoretic mobilities in a hydrated gel.
The gel suppresses convective mixing of the fluid phase through which the electrophoresis takes place and contributes molecular sieving. Commonly carried out in the presence of the anionic detergent sodium dodecylsulphate (SDS).
SDS denatures proteins so that noncovalently associating sub unit polypeptides migrate independently and by binding to the proteins confers a net negative charge roughly proportional to the chain weight.
See: SDS PAGE.
(21 Jun 1999)
pulsed-field gel electrophoresis Gel electrophoresis in which, after electrophoretic migration has begun, the current is briefly stopped and reapplied in a different orientation; allows for the purification of long DNA molecules.
Synonym: pulsed-field gel electrophoresis.
(05 Mar 2000)
pulse-field gel electrophoresis Gel electrophoresis in which, after electrophoretic migration has begun, the current is briefly stopped and reapplied in a different orientation; allows for the purification of long DNA molecules.
Synonym: pulsed-field gel electrophoresis.
(05 Mar 2000)
sol gel transformation Transition between more fluid cytoplasm (endoplasm) and stiffer gel like ectoplasm proposed as a mechanism for amoeboid locomotion: since the endoplasm cannot really be considered a simple fluid and has visco elastic properties like a gel, the term is misleading.
(18 Nov 1997)
disc gel Confusingly, nothing to do with shape, gels in which there is a discontinuity in pH or gel concentration or buffer composition.
(18 Nov 1997)
electrophoresis, agar gel Electrophoresis in which agar or agarose gel is used as the diffusion medium.
(12 Dec 1998)
electrophoresis, gel, pulsed-field Electrophoresis in which the direction of the electric field is changed periodically. This technique is similar to other electrophoretic methods normally used to separate double-stranded DNA molecules ranging in size up to tens of thousands of base-pairs. However, by alternating the electric field direction one is able to separate DNA molecules up to several million base-pairs in length.
(12 Dec 1998)
electrophoresis, gel, two-dimensional Electrophoresis in which a second perpendicular electrophoretic transport is performed on the separate components resulting from the first electrophoresis. This technique is usually performed on polyacrylamide gels.
(12 Dec 1998)
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    ÇѱÛ
  • mine layer
    ±â·Ú ºÎ¼³ÇÔ
  • nepheloid layer
    (Á¡Åä ±¸¼º¹° Å©±âÀÇ ¹Ì¼¼ÇÑ ±¤¹°ÀÌ ¶°´Ù´Ï´Â ½ÉÇØÀÇ)ÇöŹÃþ
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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    ±¸ºÐ/º¸Çè±Þ¿©
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    ±¸ºÐ/º¸Çè±Þ¿©
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