Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/30

From 2010.igem.org

(Difference between revisions)
(2010/8/30 Monday (Naoto))
(2010/8/30 Monday (Naoto))
Line 1: Line 1:
 +
{{:Team:Tokyo_Metropolitan/Header}}
==2010/8/30 Monday (Naoto)==
==2010/8/30 Monday (Naoto)==
===Experiment:electrophoresis===
===Experiment:electrophoresis===

Revision as of 04:52, 2 September 2010


Contents

2010/8/30 Monday (Naoto)

Experiment:electrophoresis

member
NEX,bambi75 and watachin

material

  • PCR production (bcsC from E.coli)
  • 1×TAE buffer
  • agarose gel

procedure
follow to protocol4

result
bands of bcsC were appeared

Experiment:separation of A.xylinus

member
naoto

material

  • A.xylinus in open wet ware media(8/25 made)

procedure

  1. take 0.5ml of A.xylinus in open wet ware media to tubes
  2. centrifuge 15000rpm/5min

Experiment:direct PCR

member
naoto

material

  • A.xylinus separated above experiment

procedure
follow to protocol3

Experiment:purification of agarose gel

member
NEX,bambi75 and watachin

material

  • bcsC from E.coli in agarose gel
  • QIAGEN

procedure
follow to protocol5

Experiment:electrophoresis

member
naoto

material

  • PCR production (bcsA from A.xylinus)
  • 1×TAE buffer
  • agarose gel

procedure
follow to protocol4

result
a band of bcsA were appeared (below bands appreared to be primer)

Experiment:purification of agarose gel

member
naoto

material

  • bcsA from A.xylinus in agarose gel
  • QIAGEN

procedure
follow to protocol5