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¿µ¹® fibrinogen ÇÑ±Û ¼¶À¯¼Ò¿ø
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¿µ¹® enzyme-linked immunoabsorbent assay ÇÑ±Û È¿¼Ò¸é¿ªÃøÁ¤¹ý
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ¼¶À¯¼Ò¿ø, ÇǺ긮³ë°Õ
  • fibrinogen degradation products
    ¼¶À¯¼Ò¿øºÐÇØ»ê¹°
  • fractional fibrinogen catabolic rate
    ºÐȹº°¼¶À¯¼Ò¿ø´ë»çÀ²
  • antibody capture enzyme-linked immunosorbent assay
    Ç×üÆ÷ȹȿ¼Ò¸é¿ªÃøÁ¤(¹ý)
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • assay
    1. ÃøÁ¤ 2. ÃøÁ¤¹ý 3. °Ë»ç, ºÐ¼®
  • biological assay
    »ý¹°ÇÐÀû°ËÁ¤
  • competitive binding assay
    °æÀïÀû°áÇպм®
  • dilution assay technique
    Èñ¼®ºÐ¼®¹ý
  • double-sandwich enzyme-linked immunosorbent assay
    °ãÈ¿¼Ò¸é¿ªÃøÁ¤(¹ý)
  • enzyme assay
    È¿¼ÒÃøÁ¤
  • enzyme-linked immunosorbent assay
    È¿¼Ò°áÇո鿪ÈíÂøÃøÁ¤(¹ý)
  • foam stability assay
    °Åǰ¾ÈÁ¤ÃøÁ¤
  • hemagglutination assay
    Ç÷±¸ÀÀÁý°Ë»ç
  • hemizona assay index
    ¹ÝÅõ¸í¶ìÃøÁ¤ÁöÇ¥
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  • ¿µ¹®
    ÇѱÛ
  • assay
    ºÐ¼®, ÃøÁ¤
  • enzyme-linked immunosorbent assay
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
  • Treponema pallidum hemaggulutination assay
    ¸Åµ¶Ç÷±¸ÀÀÁý°Ë»ç
  • fibrinogen
    ¼¶À¯¼Ò¿ø
  • fibrinogen degradation products product
    ¼¶À¯¼ÒºÐÇØ»ê¹°
  • fibrinogen degradation products product
    ¼¶À¯¼Ò¿øºÐÇØ»ê¹°
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ¼¶À¯¼Ò¿ø
  • fibrinogen consumption test
    ¼¶À¯¼Ò¿ø¼Òºñ°Ë»ç
  • fractional fibrinogen catabolic rate
    ºÐȹº°¼¶À¯¼Ò¿ø´ë»çÀ²
  • assay
    ºÐ¼®, ÃøÁ¤
  • antibody capture enzyme-linked immunosorbent assay
    Ç×üÆ÷ȹȿ¼Ò¸é¿ªÃøÁ¤¹ý
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • biological assay
    »ý¹°ÇÐÀû°ËÁ¤
  • direct fluorescent assay
    Á÷Á¢Çü±¤ºÐ¼®
  • double-sandwich enzyme-linked immunosorbent assay
    °ãÈ¿¼Ò¸é¿ªÃøÁ¤¹ý
  • enzyme assay
    È¿¼ÒÃøÁ¤
  • enzyme-linked immunosorbent assay
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
  • foam stability assay
    °Åǰ¾ÈÁ¤ÃøÁ¤
  • focus assay
    ¹ÙÀÌ·¯½ºÆ÷Ä¿½ºÃøÁ¤
  • hemagglutination assay
    Ç÷±¸ÀÀÁýÃøÁ¤(¹ý)
  • hemolytic plaque assay
    ¿ëÇ÷ÆÇÃøÁ¤¹ý, ¿ëÇ÷ÇöóÅ©ÃøÁ¤¹ý
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Fibrinogen
    ¼¶À¯¼Ò¿ø(àéë«áÈê«)
  • fractional fibrinogen catabolic rate
    ºÐȹº° ¼¶À¯¼Ò¿ø ´ë»çÀ².
  • Beckman assay
    º£Å©¸¸ºÐ¼®<--ÃøÁ¤>
  • ELISA => enzyme-linked immunosorbent assay
    ¿¤¶óÀÌÀÚ
  • Euglena assay
    ¿¬µÎ¹ú·¹ÃøÁ¤
  • Falcon assay screening test
    ÆÈÄܺм®¼±º°½ÃÇè
  • IRMA => immunoradiometric assay
    ¸é¿ª¹æ»çÃøÁ¤(¹ý)
  • Jernes plaque assay
    ¿©´Ï ¿ëÇ÷¹ÝÃøÁ¤¹ý, ¿©´Ï ÇöóÅ©ÃøÁ¤¹ý
  • Limulus assay
    ¸®¹°·¯½º ÃøÁ¤¹ý
  • Lowry assay
    ·Î¿ì¸®ÃøÁ¤(¹ý)
  • Raji cell assay
    ¶óÁö¼¼Æ÷½ÃÇè
  • SPA => spermatozoa penetration assay
    Á¤ÀÚ°üÅë½ÃÇè
  • TCD50 assay
    50%Á¾¾çÁ¶Àý¾ç
  • acetylcholine receptor antibody assay
    ¾Æ¼¼Æ¿Äݸ°¼ö¿ëü Ç×Ã¼ÃøÁ¤
  • acid phosphatase assay
    »ê¼ºÆ÷½ºÆÄŸÁ¦ ÃøÁ¤
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ¼¶À¯¼Ò¿ø(¡­áÈê«), È­À̺긮³ëÁ¨
  • fibrinogen
    ¼¶À¯¼Ò¿ø
  • fibrinogen consumption test
    ¼¶À¯¼Ò¿ø ¼Òºñ½ÃÇè(á¼Þ¨ãËúÐ).
  • fibrinogen degradation products=FDP
    ¼¶À¯¼Ò¿ø ºÐÇØ»ê¹°
  • fractional fibrinogen catabolic rate
    ºÐȹº° ¼¶À¯¼Ò¿ø ´ë»çÀ².
  • acetylcholine receptor antibody assay
    ¾Æ¼¼Æ¿Äݸ°¼ö¿ëü Ç×Ã¼ÃøÁ¤
  • acid phosphatase assay
    »ê¼ºÆ÷½ºÆÄŸÁ¦ ÃøÁ¤
  • ames assay
    ¿¡ÀÓ½ººÐ¼®
  • antibiotic assay
    Ç×»ý¹°Áú ¹ÙÀÌ¿ÀÆò°¡.
  • antigen capture assay
    Ç׿øÆ÷È¹ÃøÁ¤
  • antigenic assay
    Ç׿ø¼ººÐ¼®
  • antimicobial assay
    Ç×±ÕÁ¦ÃøÁ¤
  • assay
    Á¤·®, ¿ª°¡°ËÁ¤, È¿·Â°ËÁ¤.
  • assay
    Á¤·®, ¿ª°¡°ËÁ¤, È¿·Â°ËÁ¤
  • assay, enzyme-linked immuno(ad)sorbent (ELISA)
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ¼¶À¯¼Ò¿ø(àéë«áÈê«)
  • assay
    ¾Æ½êÀÌ
  • binding assay
    °áÇÕ(Ì¿ùê)¾Æ½êÀÌ
  • biological assay
    »ý¹°ÇÐÀû(ßæÚªùÊîÜ) ¾Æ½êÀÌ
  • competitive radioligand assay
    °æÇÕÀû(ÌæùêîÜ ¹æ»ç´É(Û¯ÞÒÒö)¸®°£µå ¾Æ½êÀÌ
  • continuous assay
    ¿¬¼Ó(Ö§áÙ)¾Æ½êÀÌ
  • coupled assay
    °ø¿ª(Íìæµ) ¾Æ¼¼ÀÌ (ÔÒ) auxiliary enzyme
  • d-assay
    d-¾Æ½êÀÌ
  • discontinuous assay
    ºÒ¿¬¼Ó(ÝÕææáÙ) ¾Æ½êÀÌ
  • dot blot assay
    Á¡(ïÃ)ºí·Ô ¾Æ¼¼ÀÌ
  • enzyme assay
    È¿¼Ò(ý£áÈ)¾Æ½êÀÌ
  • enzyme-linked immunosorbent assay
    È¿¼Ò¿¬°ü ¸é¿ªÈíÂø (ý£áÈ֤μØóæ¹ýåó·) ¾Æ½êÀÌ
  • fixed time assay
    ÀÏÁ¤½Ã°£(ìéïÒãÁÊà) ¾Æ½êÀÌ
  • hemolytic plaque assay
    ¿ëÇ÷(éÁúì) ÇöóÅ© ¾Æ½êÀÌ
  • i-assay
    i-¾Æ½êÀÌ
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ¼¶À¯¼Ò¿ø, È­À̺긮³ëÁ¨
  • assay
    Á¤·®, ¿ª°¡°ËÁ¤, È¿·Â°ËÁ¤
  • ELISA [=enzyme-linked immunosorbent assay]
    ELIZA, ¿¤¸®ÀÚ
  • enzyme-linked immunosorbent assay [=ELISA]
    ELISA, ¿¤¸®ÀÚ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
LAI assay Leukocyte Adherence Inhibition assay
ERA electrical response activity; electroencephalic response audiometry; Electroshock Research Associati...
IFA idiopathic fibrosing alveolitis; immunofluorescence assay; immunofluorescent antibody; incomplete Fr...
FDP(s)   1) Fibrinolytic split Products(= FSP)
  2) Fibrinogen Degradation Products
FBG fasting blood glucose; fibrinogen; foreign body granulomatosis
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
FDP Fibrin-fibrinogen degradation product
FB Fibrinogen
FBG Fibrinogen
FG Fibrinogen
FIB Fibrinogen
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • fibrinogen consumption test
    ¼¶À¯¼Ò¿ø ¼Òºñ ½ÃÇè
  • fractional fibrinogen catab rate
    ºÐȹº° ¼¶À¯¼Ò¿ø ´ë»çÀ²
  • acid phosphatase assay
    »ê¼º Æ÷½ºÆÄŸÁ¦ ÃøÁ¤
  • antigenic assay
    Ç׿ø¼º ºÐ¼®
  • antimicobial assay
    Ç×±ÕÁ¦ ÃøÁ¤
  • assay
    Á¤·®, ¿ª°¡ °ËÁ¤, È¿·Â °ËÁ¤
    È¥ÇÕ¹°¿¡ ÀÖ´Â ¼ººÐÀÇ ¾ç, ¶Ç´Â ¾à¹°ÀÇ »ý¹°ÇÐÀû, ¾à¸®ÇÐÀû ¿ª°¡ µîÀÇ ÃøÁ¤.
  • calcitonin assay
    Ä®½ÃÅä´Ñ ÃøÁ¤
  • carcinoembryonic antigen assay
    ¾Ï ¹è¾Æ¼º Ç׿ø ÃøÁ¤, ¾Ï¼º ¹è¾Æ¼º Ç׿ø ÃøÁ¤
  • carcinogen assay
    ¹ß¾Ï ¹°Áú °Ë»ç
  • cell adhesive matrix assay
    ¼¼Æ÷ Á¡Âø ±âÁú ºÐ¼®
  • colony formation assay
    Áý¶ô Çü¼º´É ÃøÁ¤
  • enzymatic assay
    È¿¼Ò¼º ÃøÁ¤, È¿¼Ò¼º ÃøÁ¤¹ý
  • enzyme-linked immunoadsorbent assay
    È¿¼Ò ¸é¿ª ÃøÁ¤¹ý
  • enzyme-linked immunosorbent assay
    È¿¼Ò ¸é¿ª ÃøÁ¤¹ý
  • hemolytic plaque assay
    ¿ëÇ÷¹Ý ½ÃÇè, ¿ëÇ÷¹Ý ÃøÁ¤¹ý, ¿ëÇ÷ÇöóÅ© ÃøÁ¤¹ý
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
fibrin fibrinogen degradation products <chemical> Soluble protein fragments formed by the proteolytic action of plasmin on fibrin or fibrinogen. Fdp and their complexes profoundly impair the haemostatic process and are a major cause of haemorrhage in intravascular coagulation and fibrinolysis.
Pharmacological action: antithrombins.
(12 Dec 1998)
fibrinogen <protein> Soluble plasma protein (340 kD, 46 nm long), composed of 6 peptide chains (2 each of A_, B_ and _) and present at about 2-3 mg/ml.
(12 Nov 1997)
fibrinogen-fibrin conversion syndrome <syndrome> A syndrome characterised by hypofibrinogenaemia with incoagulable blood; it may be seen in abruptio placentae, prolonged retention of a dead foetus in an Rh-isosensitised mother, haemolytic blood reactions, bilateral renal cortical necrosis, and cases of trauma.
(05 Mar 2000)
acetyl reduction assay <investigation> A technique for measuring the nitrogen fixation activity in photosynthetic organisms. It uses a flame ionisation detector and a gas chromatography apparatus to determine the reduction of acetylene to ethylene by the enzyme nitrogenase.
(06 May 1997)
Ames assay <procedure> One of a number of procedures used to test substances for likely ability to cause cancer that combines the use of animal tissue to generate active metabolites of the substance with a test for mutagenicity in bacteria.
(18 Nov 1997)
antibiotic assay <investigation> A test to determine how sensitive a bacterial or fungal strain is to arange of antibiotics bymeasuring the microbes' ability to grow in astandard dilution of each chemical.
(09 Oct 1997)
assay <procedure> The determination of the amount of a particular constituent of a mixture or of the biological or pharmacological potency of a drug.
(10 May 1997)
bandshift assay <investigation> An assay for proteins, such as transcription factors, that bind specific DNA sequences.
A labelled oligonucleotide corresponding to the recognition sequence is incubated with an appropriate nuclear protein extract and run on a nondenaturing acrylamide gel. Oligonucleotides that have been bound by proteins are retarded relative to those that are unbound.
(18 Nov 1997)
biological assay <technique> Once a pharmaceutical protein is isolated from the cells in which it was grown, researchers perform tests to measure the protein's biological activity.
It must maintain a certain minimal level of biological activity to be used for animal or clinical testing or, later, for market. Researchers also test to confirm that the isolated protein is identical to the desired protein.
(21 Mar 1998)
radioimmunoprecipitation assay Sensitive assay using radiolabelled antigens to detect specific antibodies in serum. The antigens are allowed to react with the serum and then precipitated using a special reagent such as protein a sepharose beads. The bound radiolabelled immunoprecipitate is then commonly analyzed by gel electrophoresis. Radioimmunoprecipitation assay (ripa) is often used as a confirmatory test for diagnosing the presence of HIV antibodies.
(12 Dec 1998)
radioligand assay <radiobiology> Quantitative determination of receptor (binding) proteins in body fluids or tissue using radioactively labelled binding reagents (e.g., antibodies, intracellular receptors, plasma binders).
(12 Dec 1998)
radioreceptor assay A competitive binding assay in which the binder is a membrane or tissue receptor rather than an antibody.
(05 Mar 2000)
Raji cell radioimmune assay For immune complexes; a procedure by which immune complexes adsorbed from a test serum by a standard preparation of lymphoblastoid (Raji) cells are assayed by the capacity to bind 125I-labelled antibody to immunoglobulin.
(05 Mar 2000)
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)
checkerboard assay <procedure> Variant of the Boyden chamber assay for leucocyte chemotaxis introduced by Zigmond. By testing different concentrations of putative chemotactic factor in nongradient conditions, it is possible to calculate the enhancement of movement expected due simply to chemokinesis and to compare this with the distances moved in positive and negative gradients. Good experimental design thus allows chemotaxis to be distinguished from chemokinesis.
(21 May 1997)
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  • ¿µ¹®
    ÇѱÛ
  • fibrinogen
    ºê¸®³ë°Õ;¼¶À¯¼Ò¿ø
  • assay
    ½Ã±ÝÇÏ´Ù; ºÐ¼®ÇÏ´Ù
  • assay
    ½Ã±Ý;½Ã±ÝÇÏ´Ù;ºÐ¼®;ºÐ¼®ÇÏ´Ù;½ÃÇè;½ÃÇèÇÏ´Ù;ºÐ¼®¹°
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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