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"enzyme"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • extracellular enzyme
    ¼¼Æ÷¿ÜÈ¿¼Ò
  • fibrinolytic enzyme
    ¼¶À¯¼Ò¿ëÇØÈ¿¼Ò, ÇǺ기¿ëÇØÈ¿¼Ò
  • glycolytic enzyme
    ÇØ´çÈ¿¼Ò
  • induced enzyme
    À¯µµÈ¿¼Ò
  • inhibitory enzyme
    ¾ïÁ¦È¿¼Ò
  • inorganic enzyme
    ¹«±âÈ¿¼Ò
  • intracellular enzyme
    ¼¼Æ÷³»È¿¼Ò
  • lipoclastic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • microsomal enzyme
    ¹Ì¼¼¼Òüȿ¼Ò
  • one gene/one enzyme
    ÀÏÀ¯ÀüÀÚ/ÀÏÈ¿¼Ò¼³
  • oxidative enzyme
    »êÈ­È¿¼Ò
  • phosphorylating enzyme
    ÀλêÈ­È¿¼Ò
  • proteolytic enzyme
    ´Ü¹éÁúºÐÇØÈ¿¼Ò
  • packaging enzyme
    ²Ù¸®±âÈ¿¼Ò, Æ÷ÀåÈ¿¼Ò
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • digestive enzyme
    ¼ÒÈ­È¿¼Ò
  • extracellular enzyme
    ¼¼Æ÷¿ÜÈ¿¼Ò, ±Õü¹ÛÈ¿¼Ò
  • fibrinolytic enzyme
    ¼¶À¯¼Ò¿ëÇØÈ¿¼Ò
  • glycolytic enzyme
    ÇØ´çÈ¿¼Ò
  • induced enzyme
    À¯µµÈ¿¼Ò
  • inhibitory enzyme
    ¾ïÁ¦È¿¼Ò
  • inorganic enzyme
    ¹«±âÈ¿¼Ò
  • intracellular enzyme
    ¼¼Æ÷³»È¿¼Ò
  • lipoclastic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • microsomal enzyme
    ¹Ì¼¼¼Òüȿ¼Ò
  • mucolytic enzyme
    Á¡¾×ºÐÇØÈ¿¼Ò
  • oxidative enzyme
    »êÈ­È¿¼Ò
  • packaging enzyme
    ²Ù¸®±âÈ¿¼Ò
  • periplasmic enzyme
    ¿øÇüÁú¸·ÁÖÀ§È¿¼Ò
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 14 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • heterogeneous enzyme immunoassay
    ºÒ±ÕÀÏ<--Áú>È¿¼Ò¸é¿ªÇÐÀûÃøÁ¤(¹ý)
  • homogeneous enzyme immunoassay
    ±ÕÁúÈ¿¼Ò¸é¿ªÃøÁ¤(¹ý)
  • induced enzyme
    À¯µµÈ¿¼Ò.
  • inducible enzyme
    À¯µµ(¹ß)È¿¼Ò.
  • inducible enzyme
    À¯¹ß°¡´ÉÈ¿¼Ò
  • inhibitory enzyme
    ÀúÇØÈ¿¼Ò.
  • inorganic enzyme
    ¹«±âÈ¿¼Ò(ÙíѦý£áÈ).
  • phosphorylating enzyme
    ÀλêÈ­È¿¼Ò(ìÝß« ûùý£áÈ).
  • prosthetic group-labeled enzyme
    º¸Á¶±ºÇ¥ÁöÈ¿¼Ò
  • rate limiting enzyme
    ¼ÓµµÁ¶ÀýÈ¿¼Ò(áÜöôðàï½ý£áÈ).
  • receptor destroying enzyme
    ¼ö¿ëüÆÄ±«È¿¼Ò(¡­÷òÎÕý£áÈ).
  • redox enzyme
    »êȭȯ¿øÈ¿¼Ò(ß«ûùü»êªý£áÈ).
  • reducing enzyme
    ȯ¿øÈ¿¼Ò(ü½êªý£áÈ).
  • regulatory enzyme
    Á¶ÀýÈ¿¼Ò(¡­ý£áÈ).
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • enzyme label(l)ing
    È¿¼ÒÇ¥Áö.
  • enzyme labeled antibody
    È¿¼ÒÇ¥ÁöÇ×ü.
  • enzyme labelling
    È¿¼ÒÇ¥Áö
  • enzyme linked immunosorbent assay ( ELISA)
    È¿¼Ò ¸é¿ªÃøÁ¤¹ý
  • enzyme linked immunosorbent assay (ELISA)
    È¿¼Ò¸é¿ªÃøÁ¤¹ý
  • enzyme measurement
    È¿¼ÒÃøÁ¤
  • enzyme modulator mediated immunoassay
    È¿¼ÒÁ¶Àý(º¯Á¶)¸Å°³¸é¿ªÃøÁ¤(¹ý)
  • enzyme precursor
    È¿¼ÒÀü±¸Ã¼.
  • enzyme trace substance theory
    È¿¼ÒÈçÀû¹°¼³(¡­ýÝîæÚªæò).
  • enzyme, autolytic
    ÀÚ°¡¿ëÇØÈ¿¼Ò
  • enzyme, constitutive
    ±âº»±¸¼ºÀûÈ¿¼Ò
  • enzyme, extracellular
    ±Õü¿ÜÈ¿¼Ò, ¼¼Æ÷¿ÜÈ¿¼Ò
  • enzyme, receptor destroying (RDE)
    ¼ö¿ëüÆÄ±«È¿¼Ò
  • enzyme, restriction
    Á¦ÇÑÈ¿¼Ò
  • enzyme-antibody conjugate
    È¿¼Ò-Ç×ü ¹èÇÕü
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • catheptic enzyme
    Ä«µª½ÅÈ¿¼Ò(¡­ý£áÈ).
  • constitutive enzyme
    ±¸¼ºÈ¿¼Ò(ϰà÷ý£áÈ).
  • constitutive enzyme
    ±¸¼ºÀûÈ¿¼Ò (±âº»)
  • converting enzyme inhibitor
    Àüȯȿ¼Ò¾ïÁ¦Á¦.
  • covalently modulated enzyme
    °øÀ¯°áÇÕ¸ðµâÈ­È¿¼Ò.
  • cuprein enzyme
    Å¥ÇÁ·¹ÀÎÈ¿¼Ò
  • curdling enzyme
    ÀÀÀ¯È¿¼Ò(¡­ý£áÈ).
  • cytosolic enzyme
    ¼¼Æ÷ÁúÈ¿¼Ò.
  • debrancher enzyme
    ÁöÁ¦°ÅÈ¿¼Ò(ò«ð¶ËÛý£áÈ)
  • degumming enzyme
    ÇØ±³È¿¼Ò(ú°Îïý£áÈ).
  • diastatic enzyme
    ´çÈ­È¿¼Ò(ÓØûùý£áÈ).
  • digestive enzyme
    ¼ÒÈ­È¿¼Ò(á¼ûùý£áÈ).
  • erythrocyte enzyme deficiency
    ÀûÇ÷±¸È¿¼Ò°áÇÌÁõ
  • extracellular enzyme
    ¼¼Æ÷¿ÜÈ¿¼Ò, ü¿ÜÈ¿¼Ò
  • fibrinolytic enzyme
    ¼¶À¯¼Ò¿ëÇØÈ¿¼Ò.
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • enzyme I
    È¿¼Ò(ý£áÈ) I
  • enzyme II
    È¿¼Ò(ý£áÈ) II
  • enzyme III
    È¿¼Ò(ý£áÈ) III
  • enzyme immunoassay
    È¿¼Ò ¸é¿ª(ý£áÈØóæ¹)¾Æ½êÀÌ
  • enzyme induction
    È¿¼ÒÀ¯µµ(ý£áÈë¯Óô)
  • enzyme interconversion
    È¿¼Ò »óÈ£Àüȯ (ý£áÈßÓû»ï®üµ)
  • enzyme intermediates
    È¿¼Ò Áß°£Ã¼(ý£áÈñéÊàô÷)
  • enzyme kinetics
    È¿¼Ò¿ªµ¿ÇÐ(ý£áÈæ³ÔÑùÊ)
  • enzyme labeling
    È¿¼ÒÇ¥Áö(ý£áÈøöò½)
  • enzyme modulation
    È¿¼Ò ?(ý£áÈ
  • enzyme multiplicity
    È¿¼Ò´Ù¾ç¼º(ý£áÈÒýåÆàõ)
  • enzyme multiplicity feedback inhibition
    È¿¼Ò ´Ù¾ç¼º(ý£áÈÒýåÆàõ) µÇ¸ÔÀÓ ÀúÇØ(îÁúª)
  • enzyme network
    È¿¼Ò(ý£áÈ) ³×Æ®¿öÅ©
  • enzyme nomenclature
    È¿¼Ò¸í¸í¹ý(ý£áÈ٤٣Ûö)
  • enzyme pH electrode
    È¿¼Ò(ý£áÈ) pH Àü±Ø(ï³Ð¿)
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • branching enzyme
    "ºÐÁöÈ¿¼Ò(ÝÂò«ý£áÈ), °¡ÁöÄ¡±â È¿¼Ò(ý£áÈ)"
  • breakage-reunion enzyme
    Àý´ÜÀç°áÇÕ È¿¼Ò(ï·Ó¨î¢Ì¿ùêý£áÈ)
  • CCA-enzyme
    CCA È¿¼Ò(ý£áÈ)
  • citrate cleavage enzyme
    ½ÃÆ®¸£»êÀý´ÜÈ¿¼Ò(ï·Ó¨ý£áÈ)
  • cold-sensitive enzyme
    ³Ã¹Î°¨ È¿¼Ò(Ò²ÚÂÊïý£áÈ)
  • clod-stable enzyme
    ³Ã¾ÈÁ¤ È¿¼Ò(Ò²äÌïÒý£áÈ)
  • condensing enzyme
    ÃàÇÕÈ¿¼Ò(õêùêý£áÈ)
  • conjugated enzyme
    Á¢ÇÕÈ¿¼Ò(ïÈùêý£áÈ)
  • constitutive enzyme
    ±¸¼ºÈ¿¼Ò(ϰà÷ý£áÈ)
  • converter enzyme
    Àüȯȿ¼Ò(ï®üµý£áÈ)
  • converting enzyme
    "Àüȯ È¿¼Ò(ï®üµý£áÈ), (ÔÒ) serum converting enzyme"
  • coordinated enzyme
    µ¿Á¶È¿¼Ò(ÔÒðàý£áÈ)
  • coordinated enzyme synthesis
    µ¿Á¶È¿¼ÒÇÕ¼º(ÔÒðàý£áÈùêà÷)
  • core enzyme
    ÇÙ½ÉÈ¿¼Ò(ú·ãýý£áÈ)
  • covalent enzyme-substrate complex
    È¿¼Ò±âÁú °øÀ¯°áÇÕü(ý£áÈÐñòõÍìêóÌ¿ùêô÷) (ÔÒ) enzymesubstrate compound
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
AAAE amino acid activating enzyme
ACE acetonitrile; acetylcholine esterase; acute cerebral encephalopathy; acute coronary event; adrenocor...
ACEDS angiotensin-converting enzyme dysfunction syndrome
ACEI angiotensin-converting enzyme inhibitor
AICE angiotensin I converting enzyme
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
ACE Angiotensin converting enzyme activity
ACE inhibitor angiotensin converting enzyme inhibitor
ADEPT Antibody Directed Enzyme Prodrug Therapy
AOE anti-oxidant enzyme
CoA Co-enzyme A
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • heterogeneous enzyme immunoassay
    ºÒ±ÕÀÏ È¿¼Ò ¸é¿ªÇÐÀû ÃøÁ¤, ºÒ±ÕÀÏ È¿¼Ò ¸é¿ªÇÐÀû ÃøÁ¤¹ý
  • induced enzyme
    À¯µµ È¿¼Ò
    ±âÁú ¶Ç´Â ±×¿Í ±¸Á¶ÀûÀ¸·Î ¿¬°üµÈ, À¯µµ ¹°ÁúÀÇ Àڱؿ¡ ÀÇÇÏ¿© »ý¼ºµÈ È¿¼Ò.
  • lipolytic enzyme
    Áö¹æ ºÐÇØ È¿¼Ò
  • lysosomal enzyme
    ¸®¼ÒÁ» È¿¼Ò, ¿ëÇØ ¼Òü È¿¼Ò
  • microsomal enzyme
    ¹Ì¼Òü È¿¼Ò
  • microsomal enzyme system
    ¹Ì¼Òü È¿¼Ò°è
  • neural enzyme system
    ½Å°æ È¿¼Ò°è
  • pancreatic enzyme
    Ãé È¿¼Ò
    ÃéÀå¿¡¼­ ºÐºñµÇ´Â ź¼öÈ­¹°, Áö¹æ, ´Ü¹éÁúÀ» ºÐÇØÇÏ´Â È¿¼Ò.
  • periplasmic enzyme
    ¿øÇüÁú¸· ÁÖÀ§ °ø°£ È¿¼Ò
  • phosphorylating enzyme
    ÀλêÈ­ È¿¼Ò
  • proteolytic enzyme
    ´Ü¹é ºÐÇØ È¿¼Ò
    ´Ü¹é ºÐÇØ¸¦ ÃËÁøÇÏ´Â È¿¼Ò.
  • Q enzyme
    Å¥ È¿¼Ò
    Æ÷µµ´ç-1-ÀλêÀÇ 1,6-C¿¡ ÀÛ¿ëÇÏ¿© À̰ÍÀ» ÁßÈ­½ÃŰ´Â È¿¼Ò.
  • rate-limiting enzyme
    ¼Óµµ Á¶Àý È¿¼Ò
  • receptor destroying enzyme
    ¼ö¿ëü ÆÄ±« È¿¼Ò
    ¼ö¿ëü¸¦ ÆÄ±«ÇÏ¿© ÀûÇ÷±¸ÀÇ ¹ÙÀÌ·¯½º ¿ëÇ÷¿¡ ´ëÇÑ °¨¼ö¼ºÀ» ÀÒ¾î¹ö¸®°Ô ÇÏ´Â È¿¼Ò.
  • splitting enzyme
    ºÐÇÒ È¿¼Ò
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 12 ÆäÀÌÁö: 2
enzyme regulation <biochemistry> Control of the rate of a reaction catalyzed by an enzyme by some effector (e.g., inhibitors or activators) or by alteration of some condition (e.g., pH or ionic strength).
(05 Mar 2000)
enzyme replacement therapy A type of medical treatment for patients who lack an important enzyme, the missing enzyme is injected into the patient.
(09 Oct 1997)
enzyme repression The interference in synthesis of an enzyme due to the elevated level of an effector substance, usually a metabolite, whose presence would cause depression of the gene responsible for enzyme synthesis.
(12 Dec 1998)
enzyme stabilisation Reducing the chances that an enzyme will inactivate in vitro (see enzyme inactivation) by changing the environmental conditions (such as pH, temperature, concentration of salt, etc.) or by attaching organic groups to it or changing some of its amino acid subunits.
(09 Oct 1997)
enzyme stability The extent to which an enzyme retains its structural conformation or its activity when subjected to storage, isolation, and purification or various other physical or chemical manipulations, including proteolytic enzymes and heat.
(12 Dec 1998)
enzyme-catalyzed ligation <enzyme> An enzyme-mediated joining of phosphodiester linkage of two stretches of DNA or RNA, or of peptide linkage of two polypeptides.
(05 Mar 2000)
enzyme-linked immunoabsorbent assay <investigation> The enzyme-linked immunoabsorbent assay is serologic test used as a general screening tool for the detection of antibodies to the HIV virus. Reported as positive or negative. Since false positive tests due occur (for example recent flu shot), positives will require further evaluation using the western blot. ELISA technology links an a measurable enzyme to either an antigen or antibody. In this way, it can then measure the presence of an antibody or an antigen in the bloodstream.
Acronym: ELISA
(27 Sep 1997)
enzyme-linked immunosorbent assay An immunoassay utilizing an antibody labelled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
(12 Dec 1998)
enzyme-multiplied immunoassay technique A type of immunoassay in which the ligand is labelled with an enzyme, and the enzyme-ligand-antibody complex is enzymatically inactive, allowing quantitation of unlabelled ligand.
The test uses antibodies that react only with the particular drug for which the sample is being tested. The antibodies attach themselves to the drug if it is present in the sample. It is not designed to measure amounts of the drug present, only to detect its presence or absence.
It is used predominantly, but not exclusively, for the detection of drugs of abuse in the urine.
See: competitive binding assay, enzyme-linked immunosorbent assay.
(05 Mar 2000)
enzyme-substrate complex A noncovalent complex of two molecules; often referring to the enzyme-substrate complex in an enzyme-catalyzed reaction.
Compare: central complex, Michaelis complex.
Synonym: enzyme-substrate complex.
(05 Mar 2000)
enzymes, coenzymes, and enzyme inhibitors Proteins or RNA that act as biological catalysts, their cofactors, and inhibitors.
(12 Dec 1998)
enzymes, immobilised Enzymes which are immobilised on or in a variety of water-soluble or water-insoluble matrices with little or no loss of their catalytic activity. Since they can be reused continuously, immobilised enzymes have found wide application in the industrial, medical and research fields.
(12 Dec 1998)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
malate-condensing enzyme <enzyme> An important enzyme in the glyoxylic acid cycle which reversibly catalyses the synthesis of l-malate from acetyl-CoA and glyoxylate.
Chemical name: L-Malate glyoxylate-lyase (CoA-acetylating)
Registry number: EC 4.1.3.2
(12 Dec 1998)
malic enzyme <enzyme> An enzyme that catalyses the conversion of (s)-malate and NAD+ to oxaloacetate and NADH.
Chemical name: (S)-Malate:NAD+ oxidoreductase
Registry number: EC 1.1.1.37
(12 Dec 1998)
pantoate-activating enzyme pantothenate synthetase
marker enzyme <enzyme> An enzyme that is used to identify a specific cell type, cell organelle, or cell component.
(05 Mar 2000)
reducing enzyme <enzyme> An enzyme that catalyses a reduction; since all enzymes catalyze reactions in either direction, any reductase can, under the proper conditions, behave as an oxidase and vice versa, hence the term oxidoreductase. For individual reductase's, see the specific names.
Synonym: reducing enzyme.
(05 Mar 2000)
regulatory enzyme <biochemistry> An enzyme that regulatescertain functions due to its ability to undergoa change in its catalytic activity through modification of its structure.
(09 Oct 1997)
relaxing enzyme <biochemistry> Any of several enzymes, such ashelicase, that unwind DNA prior to its replication.
(09 Oct 1997)
R enzyme <enzyme> An enzyme with action similar to that of isoamylase; it cleaves 1,6-alpha-glucosidic linkages in pullalan, amylopectin, and glycogen, and in alpha-and beta-amylase limit-dextrins of amylopectin and glycogen.
Compare: isoamylase.
Synonym: limit dextrinase, pullulanase, R enzyme.
(05 Mar 2000)
repair enzyme <enzyme, molecular biology> An enzyme that can catalyze the repair of damaged DNA; e.g., DNA ligase.
(05 Mar 2000)
repressible enzyme <biochemistry> In bacteria, an enzyme whose creation is inhibited when its reaction product is plentiful.
(09 Oct 1997)
respiratory enzyme One of those enzyme's in tissues that is a part of an oxidation-reduction system accomplishing the conversion of substrates to CO2 and H2O and the transfer of the electrons removed to O2.
(05 Mar 2000)
respiratory enzyme complexes <biochemistry> The enzymes that make up the respiratory chain: NADH Q reductase, succinate Q reductase, cytochrome reductase, cytochrome C and cytochrome oxidase.
(18 Nov 1997)
glycogen debranching enzyme system 1,4-alpha-d-glucan-1,4-alpha-d-glucan 4-alpha-d-glucosyltransferase/dextrin 6 alpha-d-glucanohydrolase. An enzyme system having both 4-alpha-glucanotransferase (ec 2.4.1.25) and amylo-1,6-glucosidase (ec 3.2.1.33) activities. As a transferase it transfers a segment of a 1,4-alpha-d-glucan to a new 4-position in an acceptor, which may be glucose or another 1,4-alpha-d-glucan. As a glucosidase it catalyses the endohydrolysis of 1,6-alpha-d-glucoside linkages at points of branching in chains of 1,4-linked alpha-d-glucose residues. Amylo-1,6-glucosidase activity is deficient in glycogen storage disease type III.
(12 Dec 1998)
restriction enzyme <enzyme, molecular biology> Class of bacterial enzymes that cut DNA at specific sites. In bacteria their function is to destroy foreign DNA, such as that of bacteriophages (host DNA is specifically modified at these sites).
Type I restriction endonucleases occur as a complex with the methylase and a polypeptide that binds to the recognition site on DNA. They are often not very specific and cut at a remote site.
Type II restriction endonucleases are the classic experimental tools. They have very specific recognition and cutting sites. The recognition sites are short, 4-8 nucleotides and are usually palindromic sequences. Because both strands have the same sequence running in opposite directions the enzymes make double stranded breaks, which, if the site of cleavage is off centre, generates fragments with short single stranded tails, these can hybridise to the tails of other fragments and are called sticky ends.
They are generally named according to the bacterium from which they were isolated (first letter of genus name and the first two letters of the specific name). The bacterial strain is identified next and multiple enzymes are given Roman numerals. For example the two enzymes isolated from the R strain of E. Coli are designated Eco RI and Eco RII.
(10 Mar 1998)
restriction enzyme cutting site <molecular biology> A specific nucleotide sequence of DNA at which a particular restriction enzyme cuts the DNA.
Some sites occur frequently in DNA (for example, every several hundred basepairs), others much less frequently (rare-cutter, for example, every 10,000 base pairs).
(10 Mar 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 2
  • Enzyme Precursors - »õâ Physiologically inactive substances that can be converted to active enzymes.
    Synonyms : Precursors, Enzyme
  • Enzyme Reactivators - »õâ Compounds which restore enzymatic activity by removing an inhibitory group bound to the reactive site of the enzyme.
    Synonyms : Reactivators, Enzyme
  • Enzyme Repression - »õâ The interference in synthesis of an enzyme due to the elevated level of an effector substance, usually a metabolite, whose presence would cause depression of the gene responsible for enzyme synthesis.
    Synonyms : Repression, Enzyme
  • Enzyme Stability - »õâ The extent to which an enzyme retains its structural conformation or its activity when subjected to storage, isolation, and purification or various other physical or chemical manipulations, including proteolytic enzymes and heat.
    Synonyms : Enzyme Stabilities, Stabilities, Enzyme, Stability, Enzyme
  • Enzyme Tests - »õâ
    Synonyms : Enzyme Test, Test, Enzyme, Tests, Enzyme
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
enzyme induction The synthesis of an enzyme at a greatly increased rate in the presence of an inducer.
Ãâó: www.genpromag.com/Glossary~LETTER~E.html
enzyme-linked immunosorbent assay A type of enzyme immunoassay (EIA) to determine the presence of antibodies to HIV in the blood or oral fluids. Repeatedly reactive (ie, two or more) ELISA test results should be validated with an independent supplemental test of high specificity. In the United States the validation test used most often is the Western Blot test.
Ãâó: www.amfar.org/cgi-bin/iowa/bridge.html
enzyme a biological catalyst. That is, a substance that increases the speed of a chemical reaction without being changed in the overall process. Enzymes are vitally important to the regulation of the chemistry of cells and organisms.
Ãâó: www.nutrabio.com/Definitions/definitions_e.htm
enzyme (a) any of numerous proteins or conjugated proteins produced by living organisms and functioning as biochemical catalysts. (b) a protein that a living organism uses in the process of degrading a specific compound. The protein serves as a catalyst in the compound's biochemical transformation.
Ãâó: www.nsc.org/ehc/glossary.htm
enzyme A protein that catalyzes a biochemical reaction.
Ãâó: xenon.che.ilstu.edu/genchemhelphomepage/glossary/e...
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
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