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"immune electron microscopy"¿¡ ´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® immune system ÇÑ±Û ¸é¿ªÃ¼°è
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  ¼¼Æ÷¼ººÐ ¹× ºÐÀÚ¼ººÐÀÇ º¹ÇÕü°è·Î¼­, ÀÌÀÇ ÀÏÂ÷±â´ÉÀº ÀÚ±â(self)¸¦ ºñÀÚ±â(not self)·ÎºÎÅÍ ±¸º°ÇÏ°í ¿ÜºÎ»ý¹° ¶Ç´Â ¹°Áú¿¡ ´ëÇØ ¹æ¾îÇϴ °ÍÀÌ´Ù. ÀÏÂ÷ÀûÀΠ¼¼Æ÷¼ººÐÀº ¸²ÇÁ±¸¿Í Å«Æ÷½Ä¼¼Æ÷À̸ç ÀÏÂ÷ÀûÀΠºÐÀÚ¼ººÐÀº Ç×ü¿Í ¸²Æ÷Ä«ÀÎÀÌ´Ù.
  
  
¿µ¹® electron microscope ÇÑ±Û ÀüÀÚÇö¹Ì°æ
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  Àü±â ¸¶´ç ¶Ç´Â Àڱ⠸¶´çÀ» ÀÌ¿ëÇÏ¿© ÀüÀÚ·ù¸¦ ÀüÀÚ ·»Áî¿¡ Áý¼Ó½ÃÄÑ, ±× Åë·Î¿¡ ³õÀΠǥº»ÀÇ »óÀ» È®´ëÇϴ ÀåÄ¡. ±¤ÇРÇö¹Ì°æº¸´Ù ÈξÀ ¶Ù¾î³­ ºÐÇØ ´É·ÂÀ» °¡Áø´Ù. 
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  • ¿µ¹®
    ÇѱÛ
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç(¹ý)
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • fluorescent microscopy
    Çü±¤Çö¹Ì°æ¹ý
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç(¹ý)
  • electron
    ÀüÀÚ
  • electron affinity
    ÀüÀÚģȭ·Â
  • electron beam
    ÀüÀÚ¼±, ÀüÀÚºö
  • electron capture
    ÀüÀÚÆ÷ȹ
  • electron carrier
    ÀüÀÚ¿î¹Ýü
  • electron configuration
    ÀüÀÚ¹èÄ¡
  • electron density
    ÀüÀڹеµ
  • electron diffraction
    ÀüÀÚȸÀý
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • immune thrombocytopenic purpura
    ¸é¿ªÇ÷¼ÒÆÇ°¨¼ÒÀÚ»ö¹Ý
  • electron
    ÀüÀÚ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • transmission electron microscope
    Åõ°úÀüÀÚÇö¹Ì°æ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ°Ë»ç
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ°Ë»ç
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ°Ë»ç¹ý
  • microscopy
    Çö¹Ì°æ°Ë»ç(¹ý)
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ°Ë»ç
  • electron affinity
    ÀüÀÚģȭ·Â
  • electron microscopic autoradiography
    ÀüÀÚÇö¹Ì°æÀÚ°¡¹æ»ç¼±¼ú
  • electron beam
    ÀüÀÚ¼±
  • electron capture
    ÀüÀÚÆ÷ȹ
  • electron carrier
    ÀüÀÚ¿î¹Ýü
  • electron configuration
    ÀüÀÚ¹èÄ¡
  • orbital electron capture
    ±ËµµÀüÀÚÆ÷ȹ
  • electron density
    ÀüÀڹеµ
  • electron diffraction
    ÀüÀÚȸÀý
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • immune electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • immune-electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý
  • immunologic electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • Darkfield microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • free electron
    ÀÚÀ¯ÀüÀÚ(í»ë¦ï³í­).
  • free electron
    ÀÚÀ¯ÀüÀÚ
  • high electron density
    °íÀüÀڹеµ(ÍÔï³í­ÚËöô).
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ(°Ë»ç)¹ý.
  • phase contrast microscopy
    À§»óÂ÷(êÈßÓó¬)Çö¹Ì°æ°Ë»ç
  • phase-contrast microscopy
    À§»óÂ÷Çö¹Ì°æ
  • polarized light microscopy
    Æí±¤Çö¹Ì°æ
  • positive electron
    ¾çÀüÀÚ
  • recoil electron
    ¹ÝµµÀüÀÚ
  • Acquiered immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª °áÇÌÁõÈıº
  • Immune complex
    ¸é¿ªº¹ÇÕü(Øóæ¹ÜÜùêô÷)
  • Immune system
    ¸é¿ªÃ¼°è(Øóæ¹ô÷ͧ)
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • immune electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • immune-electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)
  • electron microscopy
    ÀüÀÚÇö¹Ì°æ°Ë»ç(¹ý)(¡­ËþÞÛÛö).
  • electron microscopy(EM)
    ÀüÀÚÇö¹Ì°æ
  • immunologic electron microscopy
    ¸é¿ªÀüÀÚÇö¹Ì°æ¹ý.
  • odd electron ; unpaired electron
    ºÒ´ëÀüÀÚ, ºñ´ëÀüÀÚ.
  • odd electron ; unpaired electron
    ȦÀüÀÚ.
  • electron microscope, immune
    ¸é¿ªÀüÀÚÇö¹Ì°æ
  • bright field microscopy
    ¸í½Ã¾ß Çö¹Ì°æ¹ý
  • brightfield microscopy
    ¸í½Ã¾ß Çö¹Ì°æ
  • dark field microscopy
    ¾Ï½Ã¾ßÇö¹Ì°æ
  • fluorescence microscopy
    Çü±¤Çö¹Ì°æ
  • immunofluorescence microscopy
    ¸é¿ªÇü±¤Çö¹Ì°æ(°Ë»ç)¹ý.
  • light microscopy
    ±¤ÇÐ Çö¹Ì°æ
  • light microscopy
    ±¤ÇÐÇö¹Ì°æ°Ë»ç(¹ý)(¡­ËþÞÛÛö).
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Immune cause (Hemolytic anemia)
    ¸é¿ª¿øÀÎ(¿ëÇ÷¼ººóÇ÷)
    [¿¾ ¿ë¾î] ¸é¿ª¼º¿øÀÎ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • fluorescence microscopy
    Çü±¤ Çö¹Ì°æ¹ý(û«ÎÃúéÚ°ÌðÛö)
  • hemolytic immune body
    ¿ëÇ÷ ¸é¿ªÃ¼(éÁúìØóæ¹ô÷)
  • immune adherence
    ¸é¿ª ºÎÂø(Øóæ¹Ý¾ó·)
  • immune adsorbent
    ¸é¿ª ÈíÂøÁ¦(Øóæ¹ýåó·ð¥)
  • immune antibody
    ¸é¿ª Ç×ü(Øóæ¹ù÷ô÷)
  • immune clearance
    ¸é¿ª ûÁ¤(Øóæ¹ôèïä)
  • immune competent cell
    ¸é¿ª Àû°Ý ¼¼Æ÷(Øóæ¹îêÌ«á¬øà)
  • immune complex
    ¸é¿ª º¹ÇÕü(Øóæ¹ÜÜùêô÷)
  • immune conglutination
    ¸é¿ª À¯Âø ¹ÝÀÀ(Øóæ¹ë¨ó·Úãëë)
  • immune conglutinin
    ¸é¿ª(Øóæ¹)ÄÜ±Û·çÆ¼´Ñ
  • immune cytolysis
    ¸é¿ª ¼¼Æ÷¿ëÇØ(Øóæ¹á¬øàéÁú°)
  • immune deficincy disease
    ¸é¿ª °áÇÌ Áúȯ(Øóæ¹ÌÀù¹òðü´)
  • immune elimination
    ¸é¿ª À̹° Á¦°Å(Øóæ¹ì¶Úªð¶ËÛ)
  • immune globulin
    ¸é¿ª(Øóæ¹)±Û·ÎºÒ¸°
  • immune lysis
    ¸é¿ª ¿ëÇØ(Øóæ¹éÁú°)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 14 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • immune
    ¸é¿ª¼ºÀÇ
  • electron
    ÀüÀÚ
  • electron beam
    ÀüÀÚ¼±
  • electron capture
    ÀüÀÚÆ÷Âø
  • electron density
    ÀüÀڹеµ
  • electron emission
    ÀüÀÚ¹æÃâ
  • electron microscope
    ÀüÀÚÇö¹Ì°æ
  • electron pair
    ÀüÀÚ½Ö
  • electron ray
    ÀüÀÚ¼±
  • electron volt
    ÀüÀÚº¼Æ®
  • electron wave
    ÀüÀÚÆÄ
  • free electron
    ÀÚÀ¯ ÀüÀÚ
  • proton electron dipole dipole interaction
    ¾çÀÚÀüÀÚ½Ö±ØÀÚ½Ö±ØÀÚ»óÈ£¹ÝÀÀ
  • recoil electron
    ¹ÝµµÀüÀÚ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
EM early memory; ejection murmur; electromagnetic; electron micrograph; electron microscopy, electron m...
E/M electron microscope, electron microscopy; evaluation and management
MIC maternal and infant care; medical intensive care; Medical Interfraternity Conference; microscopy; mi...
EM   1) Erythro-Mycin
  2) Electron Microscopy
AEM Academic Emergency Medicine [journal]; analytical electron microscopy; ambulatory electrocardiograph...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
IEM Immune electron microscopy
SPIEM Solid phase immune electron microscopy
cryo-EM Cryo-electron microscopy
Cryo-TEM Cryo-transmission electron microscopy
EFTEM Energy-filtering transmission electron microscopy
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • immune electron microscopy
    ¸é¿ª ÀüÀÚÇö¹Ì°æ¹ý
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • scanning electron microscopy
    ÁÖ»ç ÀüÀÚÇö¹Ì°æ
    ÀüÀÚ¼±ÀÌ Ç¥º»»óÀÇ Á¡¸¶´Ù ÁÖ»çÇÏ¿© À½±Ø¼±°ü
  • microscopy
    Çö¹Ì°æ °Ë»ç¹ý
    Çö¹Ì°æÀ» ÀÌ¿ëÇÑ °Ë»ç ¶Ç´Â °üÂû.
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª °áÇÌ ÁõÈıº
    1. ÇöÀúÇÑ ¸é¿ª °áÇ̰ú ÇÔ²² ±âȸ°¨¿°, ¼Ó¹ß¼º ¾Ï ¹× ½Å°æ°è Áõ¼¼°¡ µ¿¹Ý. ¹ÙÀÌ·¯½º ÀÚü¿¡ ÀÇÇÑ º´º¯°ú ¸é¿ª´É·Â ÀúÇÏ¿¡ µû¸¥ ±âȸ °¨¿° µîÀÇ ÀÌÂ÷Àû º´º¯ÀÇ µÎ °¡Áö·Î ´ëº°. HIV¿¡ ÀÇÇØ ¹ß»ýµÇ´Â ÁúȯÀ¸·Î ½Å°æ°è°¡ Áß¿ä Ç¥ÀûÁß Çϳª. ¹ÙÀÌ·¯½º¿¡ °¨¿°µÈ »ç¶÷ÀÇ 40% Á¤µµ°¡ Áúº´ÀÌ ¹ß»ý. ¹ÙÀÌ·¯½ºÀÇ Á÷Á¢ÀûÀÎ ¿µÇâ¿¡ ÀÌÇÑ º´º¯À¸·Î´Â ¸²ÇÁ±¸¼º ¼ö¸·¿°°ú HIV ³ú¿° µîÀÌ ÀÖÀ½. 2. ÈÄõ¼º ¸é¿ª°áÇÌÁõ. Àΰ£ ¸é¿ª°áÇÌ ¹ÙÀÌ·¯½º
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • drug-induced immune complex
    ¾àÁ¦ À¯¹ß¼º ¸é¿ª º¹ÇÕü
  • ensitization 1. administration of antigen to induce a primary immune response; priming; immunization. 2. exposure to allergen that results in the development of hypersensitivity. 3. the coating of erythrocytes with antibody so that they are subject to lys
    ³»¹ø
    ƯÈ÷ ¾È°Ë ¿¬ÀÇ.
  • human rabies immune globulin
    ±¤°ßº´ ¸é¿ª ±Û·ÎºÒ¸°
    °³¿¡°Ô ¹°¸° ÈÄ ±ÕÀÇ ÁøÇàÀ» ¸·±â À§ÇØ Åõ¿©ÇÑ´Ù.
  • human serum immune globulin
    Àΰ£ Ç÷û ¸é¿ª ±Û·ÎºÒ¸°
  • immune
    ¸é¿ª
    1. ü¾× Ç×üÀÇ »ý»ê, ¼¼Æ÷¼º ¸é¿ªÀÇ ¼º¸³, ¶Ç´Â ±× ¾çÀÚ, ȤÀº ¹ÙÀÌ·¯½º °¨¿°¿¡¼­ÀÇ ÀÎÅÍÆä·Ð Ȱ¼º°ú °°ÀÌ ´Ù¸¥ ±âÁ¤ÀÇ °á°ú µî¿¡ ÀÇÇÏ¿© Áúȯ¿¡ ´ëÇÑ ÀúÇ×·ÂÀÌ ³ô¾ÆÁø »óÅÂ. 2. Ç׿ø °ø°Ý¿¡ ÀÇÇÑ Ã¼¾×¼º Ç×ü ¶Ç´Â ¼¼Æ÷¼º ¸é¿ª, ¶Ç´Â ±× ¾çÀÚÀÇ ¼º¸³. 3. ¸é¿ªÇ÷û ±Û·ÎºÒ¸°°ú °°ÀÌ Ç׿ø °ø°Ý¿¡ ´ëÀÀÇÏ¿© »ý»êµÈ °Í. 4. ¸é¿ªÀÌ µÈ °³Ã¼. 5. ƯÀÌÀû ¶Ç´Â ºñƯÀÌÀû ±âÀüÀ» ÅëÇØ °¨¿°¼º Áúȯ¿¡ ´ëÇ×ÇÏ´Â °Í.
  • immune amnesia syndrome
    ¸é¿ª ±â¾ï »ó½Ç ÁõÈıº
  • immune complex
    ¸é¿ª º¹ÇÕü
    Ç׿ø°ú Ç×üÀÇ Æ¯Á¤ °áÇÕ¹°. ¹ÙÀÌ·¯½º³ª ¼¼±Õ µî À̹°ÀÇ Ä¨ÀÔ¿¡ ´ëÇØ¼­ »ýü°¡ »ý»êÇÑ Ç×ü´Â À̹°ÀÎ Ç׿ø°ú °áÇÕÇÏ¿© ¸é¿ª º¹ÇÕü¸¦ ¸¸µç´Ù. À̴ Ž½Ä ¼¼Æ÷³ª º¸Ã¼¸¦ Ȱ¼ºÈ­ÇÏ¿© À̹°ÀÌ ¹«ÇØÇÑ °ÍÀ¸·Î ºÐÇØÇÏ´Â °ÍÀ» µµ¿Í »ýü ¹æ¾î¿¡ µµ¿òÀ» ÁØ´Ù. Á¶Á÷ Àå¾ÖÀûÀ¸·Î ÀÛ¿ëÇÏ¿© ¸é¿ª º¹ÇÕ¼º ÁúȯÀ» ÀÏÀ¸Å°±âµµ ÇÑ´Ù.
  • immune complex-mediated
    ¸é¿ª º¹ÇÕü ¸Å°³¼º
  • immune deficiency disease
    ¸é¿ª °áÇÌ Áúȯ, ¸é¿ª °áÇ̺´
    ¸é¿ª °èÅëÀ» ±¸¼ºÇÏ´Â ¿ä¼ÒÀÇ ±â´É Àå¾Ö¿¡ ÀÇÇÏ¿© ÃÊ·¡µÇ´Â Áúȯ ±º.
  • immune mechanism
    ¸é¿ª ±âÀü
  • immune reaction
    ¸é¿ª ¹ÝÀÀ
    Ç׿ø°ú Ç×ü »çÀÌÀÇ ¹ÝÀÀ.
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
immune electron microscopy Electron microscopy of biological specimens to which specific antibody has been bound.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
aperture for electron microscopy <technique> Anode aperture: The opening in the accelerating voltage anode shield of the electron gun through which the electrons must pass to irradiate the specimen. Condenser aperture: An opening in the condenser lens controlling the number of electrons entering the lens and the angular aperture of the electron beam.
The angular aperture can also be controlled by the condenser lens current. Physical objective aperture: A metallic diaphragm, with a small central hole, used to limit the cone of electrons accepted by the objective lens. This improves image-contrast since highly scattered electrons are prevented from arriving at the Gaussian image plane and therefore cannot contribute to background fog. Aplanatic. Free from spherical aberration and coma.
(05 Aug 1998)
microscopy, electron Visual and photographic microscopy in which electron beams with wavelengths thousands of times shorter than visible light are used in place of light, thereby allowing much greater magnification.
(12 Dec 1998)
microscopy, electron, scanning Microscopy in which the object is examined directly by an electron beam scanning the specimen point-by-point, giving the surface image a three-dimensional quality.
(12 Dec 1998)
microscopy, electron, scanning transmission A type of electron microscopy which scans with an extremely narrow beam that is transmitted through the sample. The detection apparatus produces an image whose brightness depends on the atomic number of the sample. It should not be confused with microscopy, electron scanning nor with microscopy, electron, transmission (see microscopy, electron).
(12 Dec 1998)
Conventional Transmission Electron Microscopy <technique> A term applied to 'normal' transmission electron microscopy imaging. The electron beam is passed through a thin film sample (typically ~1-200 nm thick). Bright field diffraction contrast images are formed with the direct (undiffracted) beam. Dark field images are formed with a selected diffracted beam. CTEM imaging is used in the general observation of samples and careful selection of the diffracting conditions of the sample will allow the analysis of defect structures within the sample.
(05 Aug 1998)
scanning electron microscopy <procedure> Technique of electron microscopy in which the specimen is coated with heavy metal and then scanned by an electron beam. The image is built up on a monitor screen (in the same way as the raster builds a conventional television image). The resolution is not so great as with transmission electron microscopy, but preparation is easier (often by fixation followed by critical point drying), the depth of focus is relatively enormous, the surface of a specimen can be seen (though not the interior unless the specimen is cracked open) and the image is aesthetically pleasing.
(18 Nov 1997)
scanning transmission electron microscopy <procedure> Method of electron microscopy in which image formation depends upon analysis of the pattern of energies of electrons that pass through the specimen. Has comparable resolving power to conventional transmission EM.
(18 Nov 1997)
electron microscopy <procedure> Any form of microscopy in which the interactions of electrons with the specimens are used to provide information about the final structure of that specimen.
In transmission electron microscopy the diffraction and adsorption of electrons as the electron beam passes normally through the specimen is imaged to provide information on the specimen.
In scanning electron microscopy an electron beam falls at a nonnormal angle on the specimen and the image is derived from the scattered and reflected electrons. Secondary X-rays generated by the interaction of electrons with various elements in the specimen may be used for electron microprobe analysis.
(18 Nov 1997)
transmission electron microscopy <technique> Those forms of electron microscopy in which electrons are transmitted through the object to be imaged, suffering energy loss by diffraction and to a small extent by absorption.
Acronym: TEM
(18 Nov 1997)
Environmental Scanning Electron Microscopy <technique> Scanning electron microscopy is performed by scanning a focused probe across the surface of the sample to be studied. In the environmental scanning electron microscopy the composition and pressure of the atmosphere around the specimen may be controlled. In favourable cases non-conductive specimens may be examined without coating, and hydrated specimens may be examined with the water still in place.
Acronym: ESEM
(05 Aug 1998)
bright field microscopy <technique> Optical microscopy, in which absorption to a great extent and diffraction to a minor extent give rise to the image, as opposed to phase contrast or interference methods of microscopy.
(18 Nov 1997)
ratio imaging fluorescence microscopy <procedure> A method of measurement of intracellular pH or intracellular calcium levels, using a fluorescent probe molecule (see fura-2), in which the two different excitation wavelengths are used and the emitted light levels compared.
If emission at one wavelength is sensitive to the intracellular ion level and emission at the other wavelength is not, then standardisation for intracellular probe concentration, efficiency of light collection, inactivation of probe and thickness of cytoplasm can all be performed automatically.
(17 Dec 1997)
reflection X-ray microscopy <technique> A method of producing enlarged images by means of X rays. In this method the radiation is totally reflected at glancing incidence from polished concave mirrors or from the curved surfaces of single crystals by Bragg reflection. The problem of aberration corrections still limits the resolution obtainable.
(05 Aug 1998)
video microscopy <technique> Microscopy that takes advantage of video as an imaging, image processing, analysing, or controlling device.
(05 Aug 1998)
phase contrast microscopy <investigation> A simple nonquantitative form of interference micoscopy of great utility in visualising live cells. Small differences in optical path length due to differences in refractive index and thickness of structures are visualised as differences in light intensity.
(18 Nov 1997)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • microscopy
    Çö¹Ì°æ °Ë»ç(»ç¿ë¹ý)
  • immune
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