Difference between revisions of "Part:BBa K3815011"
Line 15: Line 15:
  
 
<h3><font size="3"> production and purification methods </font> </h3>
 
<h3><font size="3"> production and purification methods </font> </h3>
−
[[File:RNAgel.png|300px|thumb|right|Fig1. RNA]]
+
[[File:RNAgel.png|300px|thumb|right|Fig1. <br> (1 VATPase1 2 VATPase2 3 EPH1, 4 L4440 5 VATPase1 6 VATPase2 7 EPH1 8 L4440)
 +
]]
 
<br>
 
<br>
 
We product ds RNA and purify this [2].<br>The 1L LB culture was started at 37C and  IPTG (final 0.2mM) was added when OD exceeded 0.4 to induce RNA production for 4 hours. <br>E. coli was disrupted and precipitated with NaCl, and RNA contained in the supernatant was collected by ethanol precipitation. After that, phenol-chloroform treatment was performed to purify RNA.  <br>
 
We product ds RNA and purify this [2].<br>The 1L LB culture was started at 37C and  IPTG (final 0.2mM) was added when OD exceeded 0.4 to induce RNA production for 4 hours. <br>E. coli was disrupted and precipitated with NaCl, and RNA contained in the supernatant was collected by ethanol precipitation. After that, phenol-chloroform treatment was performed to purify RNA.  <br>

Revision as of 06:19, 21 October 2021


Part of the V-ATPaseB gene of Frankliniella occidentalis to synthesize dsRNA for RNAi
This is a section of V-ATPaseB gene of Frankliniella occidentalis to synthesize dsRNA for RNAi. To product dsRNA this sequence inserted in L4440 plasmid, and transformed into HT115(DE3).

purpose

We focused on feeding RNAi to kill these insects, based on previous studies showing that oral ingestion of dsRNA can induce RNAi-induced gene knockdown in Frankliniella occidentalis[1].
Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 452
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 320


production and purification methods

Fig1.
(1 VATPase1 2 VATPase2 3 EPH1, 4 L4440 5 VATPase1 6 VATPase2 7 EPH1 8 L4440)


We product ds RNA and purify this [2].
The 1L LB culture was started at 37C and IPTG (final 0.2mM) was added when OD exceeded 0.4 to induce RNA production for 4 hours.
E. coli was disrupted and precipitated with NaCl, and RNA contained in the supernatant was collected by ethanol precipitation. After that, phenol-chloroform treatment was performed to purify RNA.

Electrophoresis in acrylamide gel was performed to confirm whether the target RNA was produced.