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"lipoprotein electrophoresis"¿¡ ´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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    ÇѱÛ
  • starch gel electrophoresis
    ³ì¸»°ÖÀü±âÀ̵¿
  • zone electrophoresis
    ±¸¿ªÀü±âÀ̵¿
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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  • low density lipoprotein
    Àú¹ÐµµÁö´Ü¹é
  • low density lipoprotein =LDL
    Àú¹ÐµµÁö´Ü¹é.
  • low density lipoprotein =LDL
    Àú¹ÐµµÁö´Ü¹éÁú.
  • plasma lipoprotein abnormalities
    Ç÷ÀåÁöÁú´Ü¹éÁúÀÌ»óÁõ.
  • very low density lipoprotein
    ±ØÀúºñÁßÁö´Ü¹é
  • very low density lipoprotein
    ÃÊÀú¹ÐµµÁö´Ü¹é(Áú)
  • very low density lipoprotein =VLDL
    ÃÊÀúºñÁßÁö(Áú)´Ü¹é(Áú).
  • very low-density lipoprotein =VLDL
    ÃÊÀú¹ÐµµÁö(Áú)´Ü¹é(Áú).
  • agarose gel electrophoresis
    ÇÑõ°ÖÀü±â¿­µ¿
  • agarose gel electrophoresis
    ¾Æ°¡·Î½º°ÖÀü±â¿µµ¿¹ý
  • capillary electrophoresis
    ¸ð¼¼°üÀü±â¿µµ¿
  • cataphoresis =electrophoresis
    Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ).
  • disc electrophoresis
    ¿øÆÇÀü±â¿µµ¿(¹ý).
  • electrophoresis
    Àü±â¿µµ¿
  • electrophoresis
    Àü±â¿µµ¿.
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  • affinity electrophoresis
    ģȭÀü±â¿µµ¿ (öÑûúï³Ñ¨ç¶ÔÑ)
  • agar gel electrophoresis
    ÇÑõ(ùÎô¸)Á©Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • block electrophoresis
    ºí·Ï Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • cellulose acetate electrophoresis
    ¾Æ¼¼Æ®»ê(ß«)¼¿·ê·Î½º Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • cons electrophoresis
    "Äܽº Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ),"
  • continuous flow electrophoresis
    ¿¬¼Ó(ææáÙ)È帧 Àü±â¿µµ¿¹ý(ï³Ñ¨ç¶ÔÑÛö)
  • cross-electrophoresis
    ±³Â÷Àü±â¿µµ¿(Îßó©ï³Ñ¨ç¶ÔÑ)
  • crossing-paper electrophoresis
    "±³Â÷¿©Áö Àü±â¿µµ¿(Îß󩿤òµï³Ñ¨ç¶ÔÑ), (ÔÒ) cross-electro-phoresis"
  • disc gel electrophoresis
    ºÒ¿¬¼Ó(ÝÕææáÙ) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • displacement electrophoresis
    "´ëÄ¡ Àü±â¿µµ¿(ÓÛöÇï³Ñ¨ç¶ÔÑ), (ÔÒ) isotachophoresis"
  • electrophoresis
    Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • field inversion gel electrophoresis
    ÀåÀüµµ(íÞï´Óî) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • flat-bed electrophoresis
    Æò»ó(øÁßÉ) Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
  • free electrophoresis
    ÀÚÀ¯ Àü±â¿µµ¿(í»ë¦ï³Ñ¨ç¶ÔÑ)
  • gradient gel electrophoresis
    ±¸¹è(ÎþÛÕ) Á© Àü±â¿µµ¿(ï³Ñ¨ç¶ÔÑ)
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IDL Intermediate Density Lipoprotein; Á߹еµ ÁöÁú ´Ü¹éÁú
LDL Low Density Lipoprotein; Àú¹Ðµµ ÁöÁú ´Ü¹éÁú
PAGE Poly-Acrylamide Gel Electrophoresis
SDS-PAGE Sodium DodecylSulfate-PolyacrylAmide Gel Electrophoresis
2-DE 2-Dimensional Electrophoresis
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CZE Capillary Zone Electrophoresis
CAE Capillary array electrophoresis
CE-LIF Capillary electrophoresis with laser-induced fluorescence detection
CE-ESI-MS Capillary electrophoresis-electrospray ionization mass spectrometry
CE-MS Capillary electrophoresis-mass spectrometry
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
lipoprotein lipase deficiency, familial A rare familial condition characterised by massive chylomicronaemia and decreased levels of other lipoproteins. It is due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyses an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood.
(12 Dec 1998)
lipoprotein Lp(a) A lipoprotein composed of an LDL particle combined with an additional protein, Lp(a) specific protein; elevated levels have been identified as a risk factor for coronary artery disease.
(05 Mar 2000)
lipoprotein polymorphism Heritable variations in low density beta-lipoproteins; the variant lipoproteins exhibit different antigenic and chemical properties when compared with normal lipoproteins.
(05 Mar 2000)
lipoprotein-x An abnormal lipoprotein which is present in large amounts in individuals suffering from obstructive liver diseases. It exists as a bilayer vesicle of equimolar phospholipids and unesterified cholesterol containing small amounts of plasma proteins (mainly albumin) in its internal aqueous compartment together with some apolipoproteins adsorbed on its surface. Separates with ldl by ultracentrifugation.
(12 Dec 1998)
low density lipoprotein <biochemistry> A lipoprotein substances (combination of a fat and a protein) which acts as a carrier for cholesterol and fats in the bloodstream.
High levels of low density lipoprotein are considered a positive risk factor for the development of coronary artery disease. Less than 130 mg/dl is desirable, 130 to 159 mg/dl is borderline high, over 160 is considered high.
Acronym: LDL
(10 Jan 1998)
low density lipoprotein receptor <biochemistry> A cell surface protein that mediates the endocytosis of low density lipoprotein by cells.
Genetic defects in low density lipoprotein receptors lead to abnormal serum levels of low density lipoprotein and hypercholesterolaemia.
(16 Mar 1998)
low-density lipoprotein receptors Receptors on the surface of cells, especially liver cells, which bind to low density lipoprotein and promote clearance of LDL from the plasma.
(05 Mar 2000)
agarose gel electrophoresis <procedure> A type of electrophoresis that uses a matrix of highly purified agar to separate large nucleotides in size.
(06 May 1997)
blood protein electrophoresis Electrophoresis applied to blood proteins.
(12 Dec 1998)
capillary electrophoresis A technique for separating compounds, a sample of a compound to beseparated is placed in a capillary tube, which is then subjected to ahigh voltage current that separates its chemical components.
(09 Oct 1997)
capillary zone electrophoresis A method for separating molecules extremely rapidly based on their electrophoretic mobility.
(05 Mar 2000)
gamaglobulin electrophoresis <investigation> A test that detects and measures the various immunoglobulins in the blood. In the normal assay no monoclonal antibodies are detected. In multiple myeloma and chronic lymphocytic leukaemia a single clone of lymphocytes can produce one type of immunoglobulin that is detected in the electrophoresis as monoclonal (made by one cell clone).
(27 Sep 1997)
gel electrophoresis <molecular biology> Electrophoresis using a gel supporting phase. Usually applied to systems where the gel is based on polyacrylamide.
See: electrophoresis.
(05 May 1997)
carrier electrophoresis Electrophoresis done on a carrier (such as paper, polyacrylamide gel, etc.).
(05 Mar 2000)
cell electrophoresis <technique> A method for estimating the surface charge of a cell by looking at its rate of movement in an electrical field. Almost all eukaryotic cells have a net negative surface charge.
Measurement is complicated by the streaming potential at the wall of the chamber itself and by the fact that the cell is surrounded by a layer of fluid (see double layer).
The electrical potential measured (the zeta potential) is actually some distance away from the plasma membrane. One of the more useful modifications is to systematically vary the pH of the suspension fluid to determine the pK of the charged groups responsible (mostly carboxyl groups of sialic acid).
(26 Mar 1998)
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