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ºÐ¼®È­ÇнÇÇè Report05ÃÖÁ¾

ºÐ¼®È­ÇнÇÇè Report05ÃÖÁ¾

Determination of sodium carbonate and sodium hydrogen carbonate in a sample (Determination of alkalinity) / Report-05 1. Title: Determination of sodium carbonate and sodium hydrogen carbonate in a sample (Determination of alkalinity) 2. Date :2xxx.04.12/ Temperature : 21.7¡É / Humidity : 30£¥ 3. Name: / Co-workers: 4. Principle & Object - winkler ¹ý ¡¦
ÀÚ¿¬°úÇÐ   11page   2,000 ¿ø
ºÐ¼®È­ÇнÇÇè Report01

ºÐ¼®È­ÇнÇÇè Report01

Use of analytical balance and glass wares / Report- 01 1. Title: Use of analytical balance and glass wares 2. Date : 2xxx³â 3¿ù 15ÀÏ/ Temperature :21.6¡É/ Humidity : 30£¥ 3. Name:/ Co-workers: 4. Principle & Object 4-1. Principle -Á¤·® ºÐ¼® ¼¼È­ ÆíÁýºÎ, ¡ºÈ­ÇÐ ´ë»çÀü¡», 2001.05.20, 120-121p : ½Ã·á ÁßÀÇ °¢ ¼ººÐ ¹°ÁúÀÇ ¾çÀû °ü°è¸¦ ±¸ÇÒ ¸ñÀûÀ¸·Î Çϴ¡¦
ÀÚ¿¬°úÇÐ   11page   2,000 ¿ø
ºÐ¼®È­ÇнÇÇè Report02

ºÐ¼®È­ÇнÇÇè Report02

Preparation & standardization of 0.1 M HCl(aq) / Report-02 1. Title: Preparation & standardization of 0.1 M HCl(aq) 2. Date :2xxx.03.22/ Temperature : 21.8¡É / Humidity : 26£¥ 3. Name: / Co-workers: 4. Principle & Object 4-1. Principle -¸¸µé±â (35£¥ HCl, d¡ë1.175 , Mw ¡ë36.461)
ÀÚ¿¬°úÇÐ   12page   2,000 ¿ø
ºÐ¼®È­ÇнÇÇè Report04 ÃÖÁ¾

ºÐ¼®È­ÇнÇÇè Report04 ÃÖÁ¾

Determination of acidity in vinegar & value of weak acid / Report-04 1. Title: Determination of acidity in vinegar &value of weak acid 2. Date :2xxx.04.05/ Temperature : 20.8¡É / Humidity : 15£¥ 3. Name: / Co-workers: 4. Principle & Object - Ç¥ÁØÈ­(Standardization) °úÁ¤ ÀûÁ¤¹ÝÀÀ +¡æ + ⇌ + +⇌+
ÀÚ¿¬°úÇÐ   24page   3,500 ¿ø
ºÐ¼®È­ÇнÇÇè Report03 ÃÖÁ¾

ºÐ¼®È­ÇнÇÇè Report03 ÃÖÁ¾

Preparation & standardization of free carbonated 0.1 M NaOH / 1. Title: Preparation & standardization of free carbonated 0.1 M NaOH 2. Date :2xxx.03.29/ Temperature : 23.2¡É / Humidity : 24£¥ 3. Name:/ Co-workers: 4. Principle & Object - Ç¥ÁØÈ­(Standardization) °úÁ¤ ÀûÁ¤¹ÝÀÀ¨ç +¡æ+ (PHP, Mw¡ë204.22) ¡Õ (Mw¡ë40.01) ¡ë PHP Ī·®°ª, ¡ëÁ¾¸»Á¡±îÁöÀÇ ¡¦
ÀÚ¿¬°úÇÐ   21page   3,000 ¿ø
DNA Replication

DNA Replication

DNA Replication ¿¡ ´ëÇÑ ÀÚ·áÀÔ´Ï´Ù. DNAƯ¡°úReplication / ¥° DNA Replication 󰊱 Replication Forks 󰊲 The geometry of replication of DNA 󰊳 RNA Primers ¥± Enzymes of DNA replication 󰊱 Helicase(dnaB protein) 󰊲 Topoisomerase 󰊳 Primease 󰊴 DNA polymerase ¥°,¥±,¥² 󰊵 DNA Ligase 󰊶 ¡¦
ÀÚ¿¬°úÇÐ   9page   1,000 ¿ø
DNAº¹Á¦(replication)

DNAº¹Á¦(replication)

DNAº¹Á¦(replication)¿¡ ´ëÇÑ ÀÚ·áÀÔ´Ï´Ù. DNAº¹Á¦¿ÍÀü»ç / 1.Á¤ÀÇ DNAÀÇ º¹Á¦´Â ¸ð¼¼Æ÷ÀÇ À¯ÀüÁ¤º¸¸¦ µþ¼¼Æ÷·Î Á¤È®È÷ Àü´ÞÇÏ´Â ¸ÞÄ«´ÏÁòÀÌ´Ù. 2.DNA º¹Á¦ÀÇ Æ¯¼º 1) º¹Á¦´Â ¹Ýº¸Á¸Àû ¹æ½ÄÀ¸·Î ÀϾ´Ù. DNA º¹Á¦´Â ¹Ý º¸Á¸Àû º¹Á¦ ÀÌ´Ù. ÀÌ º¹Á¦ ¾ç½Ä¿¡¼­ °¢°¢ ¾î¹öÀÌ »ç½½Àº »õ·Î¿î µþ »ç½½ÀÇ ÇÕ¼ºÀ» À§ÇÑ ÁÖÇüÀÌ µÈ´Ù. º¹Á¦´Â DNA ÁßÇÕÈ¿¼Ò(DNA polymerase)°¡ »õ·Î¿î ¿°±â¸¦ Çϳª¾¿¡¦
ÀÚ¿¬°úÇÐ   9page   1,000 ¿ø
DNA repair (ȸº¹)

DNA repair (ȸº¹)

DNA repair (ȸº¹) DNA_ȸº¹¿¡_°üÇؼ­ / ¸ñÂ÷ ¾øÀ½. / DNA repair (ȸº¹) À¯ÀüÀûÀÎ º¯È­´Â »ý¹°¿¡°Ô ´Ù¾ç¼ºÀ» ºÎ¿©ÇÏ°í, ´Ù¾çÇÑ ¼­½Äȯ°æ¿¡ ÀûÀÀÇØ »ì ¼ö ÀÖ°Ô Çß´Ù. ±×·¯³ª ´Ü±âÀûÀÎ Ãø¸é¿¡¼­ »ý¹°°³Ã¼ÀÇ °üÁ¡¿¡¼­º¸¸é À¯ÀüÀûÀÎ º¯È­´Â °ÅÀÇ ´ëºÎºÐ À¯ÇØÇѵ¥, º¹ÀâÇÏ°í ¹Ì¼¼ÇÏ°Ô Á¶ÀýµÇ´Â ¹ß»ý°úÁ¤À» °®´Â ´Ù¼¼Æ÷ »ý¹°ÀÇ °æ¿ì¿¡ ¼­´Â ´õ¿í ±×·¯ÇÏ´Ù. °³Ã¼µéÀÌ »ýÁ¸ÇÏ°í »ý½ÄÇÒ ¼ö ÀÖ¡¦
ÀÚ¿¬°úÇÐ   3page   1,000 ¿ø
Repair of the Extensor Tendon System

Repair of the Extensor Tendon System

Digital extensor systemÀÇ terminal insertionÀÎ lateral bandÀÇ attachment ºÎÀ§°¡ disrup... / Digital extensor systemÀÇ terminal insertionÀÎ lateral bandÀÇ attachment ºÎÀ§°¡ disruptionµÇ¸é DIP jt.ÀÇ active extensionÀÌ ¼Ò½ÇµÇ°í distal phalanx°¡ ²©ÀÌ°Ô µÈ´Ù ¡æ ¡°mallet finger¡± deformity ∙ ´ëºÎºÐÀÇ DIP jt.ÀÇ extensor tendonÀÇ disruptionÀº closed typeÀÌ°í¡¦
ÀÚ¿¬°úÇÐ   7page   1,000 ¿ø
Àü±â ¿µµ¿ °á°ú Report

Àü±â ¿µµ¿ °á°ú Report

Çö󽺹̵å DNA¿Í PCR »ý»ê¹°À» Àü±â¿µµ¿À» ÅëÇØ È®ÀÎÇÏ´Â ½ÇÇè / ¥°. ±âº»Á¤º¸ ¥±. ¼­·Ð (Introduction) 1. PCR (polymerase chain reaction) 1-1. PCRÀÇ ¿ø¸® 1-2. PCRÀÇ °úÁ¤ 1-3. PCRÀÇ ÁÖÀç·á 2. PCR °á°ú È®ÀÎ (Àü±â¿µµ¿, electropH oresis) 3. Àü±â¿µµ¿ÀÇ Á¾·ù 3-1. À̵¿ °è¸é Àü±â¿µµ¿¹ý (Moving boundary electrophoresis) 3-2. ¶ì Àü±â¿µµ¿¹ý (Zone electrophoresis) 3-3. ºÒ¿¬¡¦
ÀÚ¿¬°úÇÐ   16page   3,000 ¿ø




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