Haynes Lab:Notebook/Engineering PC-TFs/2013/02/13
From OpenWetWare
< Haynes Lab:Notebook | Engineering PC-TFs | 2013 | 02(Difference between revisions)
(Autocreate 2013/02/13 Entry for Haynes_Lab:Notebook/Engineering_PC-TFs) |
Current revision (01:18, 16 February 2013) (view source) (→Summary) |
||
| (One intermediate revision not shown.) | |||
| Line 7: | Line 7: | ||
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### --> | <!-- ##### DO NOT edit above this line unless you know what you are doing. ##### --> | ||
==Summary== | ==Summary== | ||
| - | |||
| + | * '''Perform BsmBI/ T4 ligase mediated assembly''' | ||
| + | * BsmBI cuts the DNA fragments and creates complementary overhangs. | ||
| + | * Complementary sticky ends anneal via base pairing. | ||
| + | * T4 ligase seals gaps in the phosphodiester DNA backbone. | ||
| + | {| {{table}} | ||
| + | | bgcolor="grey" | Reagent | ||
| + | | bgcolor="grey" | Vol. | ||
| + | | rowspan=7 | '''Thermal cycling''' | ||
| + | * [45°C, 2 min.; 16°C 5 min.] x25 | ||
| + | * 60°C, 10 min. | ||
| + | * 80°C, 20 min. | ||
| + | * 4°C, ∞ | ||
| + | |- | ||
| + | | 20 fmol (1 μL) of each DNA part || up to 8.0 | ||
| + | |- | ||
| + | | 10x T4 ligase buffer (Promega) || 1.0 | ||
| + | |- | ||
| + | | T4 ligase (NEB) || 0.25 | ||
| + | |- | ||
| + | | BsmBI || 0.5 | ||
| + | |- | ||
| + | | dH<sub>2</sub>O || 0.25 | ||
| + | |- | ||
| + | | || 10.0 μL | ||
| + | |} | ||
| + | {| {{table}} border="1" cellspacing="3" <!-- Golden Gate Rxn. table --> | ||
| + | |- valign="top" | ||
| + | | bgcolor="grey" | Reagent | ||
| + | | bgcolor="grey" | 1 | ||
| + | |- | ||
| + | | gg2 pSB1A3 || 1.0 | ||
| + | |- | ||
| + | | gg3 hPCD || 1.0 | ||
| + | |- | ||
| + | | BL01 || 1.0 | ||
| + | |- | ||
| + | | 10x ligase buffer || 1.0 | ||
| + | |- | ||
| + | | NEB T4 lgase || 0.25 | ||
| + | |- | ||
| + | | BsmBI || 0.5 | ||
| + | |- | ||
| + | | dH<sub>2</sub>O || 5.25 | ||
| + | |- | ||
| + | | Total|| 10.0 | ||
| + | |} | ||
| + | |||
| + | Could not perform bacterial transformation because SOC medium was in freezer. Vi performed BsmBI/T4 ligase and bacterial transformation for BL01 and hPCD and there were no colonies on plates. | ||
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### --> | <!-- ##### DO NOT edit below this line unless you know what you are doing. ##### --> | ||
Current revision
Main project page Previous entry Next entry
| ||||||||||||||||||||||||||||||||||
Summary
Could not perform bacterial transformation because SOC medium was in freezer. Vi performed BsmBI/T4 ligase and bacterial transformation for BL01 and hPCD and there were no colonies on plates. | ||||||||||||||||||||||||||||||||||



