Team:USyd-Australia/Notebook/Primers
From 2014.igem.org
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<tr><td> <h2>Primers</h2></td></tr> | <tr><td> <h2>Primers</h2></td></tr> | ||
<tr><td> | <tr><td> | ||
- | <p>All primers were | + | <p>All primers were supplied by IDT.</p> |
<p>Primers were reconstituted in TE buffer to a stock concentration of 500μM. This is to minimise the number of freeze-thaw cycles that the primers undergo when being used. Dilutions were made to produce working primer stocks of 50μM or 10μM as required.</p> | <p>Primers were reconstituted in TE buffer to a stock concentration of 500μM. This is to minimise the number of freeze-thaw cycles that the primers undergo when being used. Dilutions were made to produce working primer stocks of 50μM or 10μM as required.</p> | ||
<p>To make 500μM stocks, Volume to add=(2x number of nMoles) μL | <p>To make 500μM stocks, Volume to add=(2x number of nMoles) μL | ||
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<tr><th width="10%">Name</th><th width="50%">Sequence (5'-3')</th><th width="10%">Theoretical Tm</th><th>Purpose</th></tr> | <tr><th width="10%">Name</th><th width="50%">Sequence (5'-3')</th><th width="10%">Theoretical Tm</th><th>Purpose</th></tr> | ||
<tr><td><a name="iGEM10"></a>iGEM10</td><td>AGCTTTCGCTAAGGATGATTTCTGGA</td><td>58.2C</td><td>Screening and sequencing</td></tr> | <tr><td><a name="iGEM10"></a>iGEM10</td><td>AGCTTTCGCTAAGGATGATTTCTGGA</td><td>58.2C</td><td>Screening and sequencing</td></tr> | ||
- | <tr><td>iGEM16</td><td>GAGTGCCACCTGACGTCTAAGAAACC</td><td>60.9C</td><td>For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM <a href="http://parts.igem.org/Part:BBa_G00100">VF2</a> primer</td></tr> | + | <tr><td><a name="iGEM16"></a>iGEM16</td><td>GAGTGCCACCTGACGTCTAAGAAACC</td><td>60.9C</td><td>For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM <a href="http://parts.igem.org/Part:BBa_G00100">VF2</a> primer</td></tr> |
- | <tr><td>iGEM25</td><td>CCCTGATTCTGTGGATAACCGTATTACCG</td><td>60.0C</td><td>For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM <a href="http://parts.igem.org/Part:BBa_G00101">VR</a> primer</td></tr> | + | <tr><td><a name="iGEM25"></a>iGEM25</td><td>CCCTGATTCTGTGGATAACCGTATTACCG</td><td>60.0C</td><td>For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM <a href="http://parts.igem.org/Part:BBa_G00101">VR</a> primer</td></tr> |
- | <tr><td>iGEM1401</td><td>GGGAAGCTTTCTTAGACGTCAGGTGGCACTTTTCGG</td><td>66.3C </td><td> pBBR replicon</td></tr> | + | <tr><td><a name="iGEM1401"></a>iGEM1401</td><td>GGGAAGCTTTCTTAGACGTCAGGTGGCACTTTTCGG</td><td>66.3C </td><td> pBBR replicon</td></tr> |
- | <tr><td>iGEM1402</td><td>TTTGGATCCTATGCTGCTGGCTACCCTGTGGAAC</td><td>66.5C</td><td>pBBR replicon</td></tr> | + | <tr><td><a name="iGEM1402"></a>iGEM1402</td><td>TTTGGATCCTATGCTGCTGGCTACCCTGTGGAAC</td><td>66.5C</td><td>pBBR replicon</td></tr> |
- | <tr><td>iGEM1403</td><td>GTTCCACAGGGTAGCCAGCAGCATAGGATCCAAAGA</br>GTGCCACCTGACGTCTAAGAAACC</td><td>71.2C</td><td>primers for pSB prefix/suffix</td></tr> | + | <tr><td><a name="iGEM1403"></a>iGEM1403</td><td>GTTCCACAGGGTAGCCAGCAGCATAGGATCCAAAGA</br>GTGCCACCTGACGTCTAAGAAACC</td><td>71.2C</td><td>primers for pSB prefix/suffix</td></tr> |
- | <tr><td>iGEM1404</td><td>CCGAAAAGTGCCACCTGACGTCTAAGAAAGCTTCCC</br>CCTGATTCTGTGGATAACCGTATTACCG</td><td>70.3</td><td>primers for pSB prefix/suffix</td></tr> | + | <tr><td><a name="iGEM104"></a>iGEM1404</td><td>CCGAAAAGTGCCACCTGACGTCTAAGAAAGCTTCCC</br>CCTGATTCTGTGGATAACCGTATTACCG</td><td>70.3</td><td>primers for pSB prefix/suffix</td></tr> |
- | <tr><td>iGEM1405</td><td>GAGGTCGGACAGTATATTGAAACGTCAGGAGTCTAG</br> | + | <tr><td><a name="iGEM1405"></a>iGEM1405</td><td>GAGGTCGGACAGTATATTGAAACGTCAGGAGTCTAG</br>A<u>TACCGAGGGACAGACTACCAACTCACA</u></td><td> </td><td>primers for gene cassette circularisation (attC-aeBlue-aacC1)</td></tr> |
- | <tr><td>iGEM1406</td><td> GTATCTAGACTCCTGACGTTTCAATATACTGTCCG</br> | + | <tr><td><a name="iGEM1406"></a>iGEM1406</td><td> GTATCTAGACTCCTGACGTTTCAATATACTGTCCG</br>ACCTC<u>TTATTAGGTGGCGGTACTTGGGTCG</u></td><td> </td><td>primers for gene cassette circularisation (attC-aeBlue-aacC1)</td></tr> |
- | <tr><td>iGEM1407 </td><td>CTATATCTATGATCTCGCAGTCTCC </td><td>53.8C </td><td> PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening</td></tr> | + | <tr><td><a name="iGEM1407"></a>iGEM1407 </td><td>CTATATCTATGATCTCGCAGTCTCC </td><td>53.8C </td><td> PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening</td></tr> |
- | <tr><td>iGEM1408</td><td>GCCTTTTGCTCACATGTTCTTTC</td><td>55.2C</td><td>PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening</td></tr> | + | <tr><td><a name="iGEM1408"></a>iGEM1408</td><td>GCCTTTTGCTCACATGTTCTTTC</td><td>55.2C</td><td>PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening</td></tr> |
- | <tr><td>iGEM1409 </td><td> GTTTTTTTGGATGGAGTGAAACGATGGCGATTG </td><td> 61.7C </td><td> Amplification of iGEM-IntI1 gBlock forward primer</td></tr> | + | <tr><td><a name="iGEM1409"></a>iGEM1409 </td><td> GTTTTTTTGGATGGAGTGAAACGATGGCGATTG </td><td> 61.7C </td><td> Amplification of iGEM-IntI1 gBlock forward primer</td></tr> |
- | <tr><td>iGEM1410 </td><td> TGACACCTTGCCCTTTTTTGCCG </td><td> 60.9C </td><td> Amplification of iGEM-IntI1 gBlock reverse primer</td></tr> | + | <tr><td><a name="iGEM1410"></a>iGEM1410 </td><td> TGACACCTTGCCCTTTTTTGCCG </td><td> 60.9C </td><td> Amplification of iGEM-IntI1 gBlock reverse primer</td></tr> |
- | <tr><td>iGEM1411 </td><td> GTTTTTTTGGATGGAGTGAAACGATGGCGATTG </td><td> 61.7C </td><td> Gblock primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1411"></a>iGEM1411 </td><td> GTTTTTTTGGATGGAGTGAAACGATGGCGATTG </td><td> 61.7C </td><td> Gblock primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1412 </td><td> TGACACCTTGCCCTTTTTTG </td><td> 53.9C </td><td> Gblock primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1412"></a>iGEM1412 </td><td> TGACACCTTGCCCTTTTTTG </td><td> 53.9C </td><td> Gblock primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1413 </td><td> GACATTGCCGTCACTGCGTC </td><td> 59.1C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1413"></a>iGEM1413 </td><td> GACATTGCCGTCACTGCGTC </td><td> 59.1C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1414 </td><td> TGGTCCAGAACCTTGACCGAAC </td><td> 59.2C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1414"></a>iGEM1414 </td><td> TGGTCCAGAACCTTGACCGAAC </td><td> 59.2C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1415 </td><td> AACCGAGGATGCGAACCACTTC </td><td> 59.7C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1415"></a>iGEM1415 </td><td> AACCGAGGATGCGAACCACTTC </td><td> 59.7C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1416 </td><td> CCTTCAAACGTGCCGTAGAACAAGC </td><td> 60.4C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> | + | <tr><td><a name="iGEM1416"></a>iGEM1416 </td><td> CCTTCAAACGTGCCGTAGAACAAGC </td><td> 60.4C </td><td> Junction primers for IntI1 in pSAM-R</td></tr> |
- | <tr><td>iGEM1417 </td><td> AAATACTAGTAGCGGCCGCTGCAGTCCGGCAAAA</br>AAG </td><td> 67.6C </td><td> Linearisation of pSB1C3, containing full BioBrick prefix and suffix</td></tr> | + | <tr><td><a name="iGEM1417"></a>iGEM1417 </td><td> AAATACTAGTAGCGGCCGCTGCAGTCCGGCAAAA</br>AAG </td><td> 67.6C </td><td> Linearisation of pSB1C3, containing full BioBrick prefix and suffix</td></tr> |
- | <tr><td>iGEM1418 </td><td> AAACTCTAGAAGCGGCCGCGAATTCCAGAAATCA</br>TCCTTAGC </td><td> 66.9C </td><td> Linearisation of pSB1C3, containing full BioBrick prefix and suffix</td></tr> | + | <tr><td><a name="iGEM1418"></a>iGEM1418 </td><td> AAACTCTAGAAGCGGCCGCGAATTCCAGAAATCA</br>TCCTTAGC </td><td> 66.9C </td><td> Linearisation of pSB1C3, containing full BioBrick prefix and suffix</td></tr> |
- | <tr><td>iGEM1419 </td><td> TTTGAATTCGCGGCCGCTTCTAGAGTACCGAGGG</br>ACAGAC </td><td> 68.9C </td><td> Amplification of aeBlue gBlock. Forward primer.</td></tr> | + | <tr><td><a name="iGEM1419"></a>iGEM1419 </td><td> TTTGAATTCGCGGCCGCTTCTAGAGTACCGAGGG</br>ACAGAC </td><td> 68.9C </td><td> Amplification of aeBlue gBlock. Forward primer.</td></tr> |
- | <tr><td>iGEM1420 </td><td> GGGCTGCAGCGGCCGCTACTAGTATTATTAGGTGG </td><td> 67.4C </td><td> Amplification of aeBlue gBlock. Reverse primer.</td></tr> | + | <tr><td><a name="iGEM1420"></a>iGEM1420 </td><td> GGGCTGCAGCGGCCGCTACTAGTATTATTAGGTGG </td><td> 67.4C </td><td> Amplification of aeBlue gBlock. Reverse primer.</td></tr> |
- | <tr><td>iGEM1421 </td><td> GGGAATTCAAATCTAGAGACACCATCG </td><td> 57.1C </td><td> Amplification of LacI-Plac-AttI gBlock. Forward primer</td></tr> | + | <tr><td><a name="iGEM1421"></a>iGEM1421 </td><td> GGGAATTCAAATCTAGAGACACCATCG </td><td> 57.1C </td><td> Amplification of LacI-Plac-AttI gBlock. Forward primer</td></tr> |
- | <tr><td>iGEM1422 </td><td> CCTGCAGTTTACTAGTTTTGCCTAACTTTGTTTTAG </td><td> 59.4C </td><td> Amplification of LacI-Plac-AttI gBlock. Reverse primer</td></tr> | + | <tr><td><a name="iGEM1422"></a>iGEM1422 </td><td> CCTGCAGTTTACTAGTTTTGCCTAACTTTGTTTTAG </td><td> 59.4C </td><td> Amplification of LacI-Plac-AttI gBlock. Reverse primer</td></tr> |
- | <tr><td>iGEM1423 </td><td> CAGGCTTTACACTTTATGCTTCCG </td><td> 56.3C </td><td> lacI-Plac-attI RHJ-F right hand junction forward primer (use with iGEM25)</td></tr> | + | <tr><td><a name="iGEM1423"></a>iGEM1423 </td><td> CAGGCTTTACACTTTATGCTTCCG </td><td> 56.3C </td><td> lacI-Plac-attI RHJ-F right hand junction forward primer (use with iGEM25)</td></tr> |
- | <tr><td>iGEM1424 </td><td> AATGTAATTCAGCTCCGCCATC</td><td> 55.5C </td><td> lacI-Plac-attI LHJ-R left hand junction reverse primer (use with iGEM16)</td></tr> | + | <tr><td><a name="iGEM1424"></a>iGEM1424 </td><td> AATGTAATTCAGCTCCGCCATC</td><td> 55.5C </td><td> lacI-Plac-attI LHJ-R left hand junction reverse primer (use with iGEM16)</td></tr> |
- | <tr><td>iGEM1425 </td><td> AAATCTAGATGGCGCGGCTTAACTCAGGTGTTAG</br>GCTTAGGAGGCTCAAGTATGGGCAT </td><td> 70.7C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1426.</td></tr> | + | <tr><td><a name="iGEM1425"></a>iGEM1425 </td><td> AAATCTAGATGGCGCGGCTTAACTCAGGTGTTAG</br>GCTTAGGAGGCTCAAGTATGGGCAT </td><td> 70.7C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1426.</td></tr> |
- | <tr><td>iGEM1426 </td><td> AAAACTAGTGGCGTCGGCTTGGACGAATTGTTAG</br>GCTTAGGTGGCGGTACTTGGGTC </td><td> 71.4C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1425.</td></tr> | + | <tr><td><a name="iGEM1426"></a>iGEM1426 </td><td> AAAACTAGTGGCGTCGGCTTGGACGAATTGTTAG</br>GCTTAGGTGGCGGTACTTGGGTC </td><td> 71.4C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1425.</td></tr> |
- | <tr><td>iGEM1427 </td><td> TTTTCTAGAGTTTGATGTTATGGAGCAGCAACG </td><td> 60.2C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1428. Alternative to iGEM1424.</td></tr> | + | <tr><td><a name="iGEM1427"></a>iGEM1427 </td><td> TTTTCTAGAGTTTGATGTTATGGAGCAGCAACG </td><td> 60.2C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1428. Alternative to iGEM1424.</td></tr> |
- | <tr><td>iGEM1428 </td><td> TTTACTAGTGCAAAAAGGCAGCAATTATGAGCC </td><td> 60.9C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1427. Alternative to iGEM1426.</td></tr> | + | <tr><td><a name="iGEM1428"></a>iGEM1428 </td><td> TTTACTAGTGCAAAAAGGCAGCAATTATGAGCC </td><td> 60.9C </td><td> For making aacC1 gene cassettes from Tn1696. Use with iGEM1427. Alternative to iGEM1426.</td></tr> |
- | <tr><td>NVC71 </td><td> CTAAGAATCCATAGTCCAACTCC </td><td> 52.4C </td><td> aadB gene, rvs primer for junction screen</td></tr> | + | <tr><td><a name="NVC71"></a>NVC71 </td><td> CTAAGAATCCATAGTCCAACTCC </td><td> 52.4C </td><td> aadB gene, rvs primer for junction screen</td></tr> |
- | <tr><td>NVC92b </td><td> CACGCAAGACCTCAACCTTTTCC </td><td> 58.6C </td><td> aadB gene, rvs primer for junction screen</td></tr> | + | <tr><td><a name="NVC92b"></a>NVC92b </td><td> CACGCAAGACCTCAACCTTTTCC </td><td> 58.6C </td><td> aadB gene, rvs primer for junction screen</td></tr> |
- | <tr><td>NVC158 </td><td> GATACCTTGTGCGGCTATGTCTG </td><td> 57.6C </td><td> pUS41/44, left of cloning site</td></tr> | + | <tr><td><a name="NVC158"></a>NVC158 </td><td> GATACCTTGTGCGGCTATGTCTG </td><td> 57.6C </td><td> pUS41/44, left of cloning site</td></tr> |
- | <tr><td>NVC159 </td><td> GCCGCCTTGGGCCGGGTGATGTC </td><td> 69.2C </td><td> pUS41/44, right of cloning site</td></tr> | + | <tr><td><a name="NVC159"></a>NVC159 </td><td> GCCGCCTTGGGCCGGGTGATGTC </td><td> 69.2C </td><td> pUS41/44, right of cloning site</td></tr> |
</table> | </table> | ||
</html> | </html> | ||
{{Team:USyd-Australia/Footer}} | {{Team:USyd-Australia/Footer}} |
Latest revision as of 03:32, 18 October 2014
Primers |
All primers were supplied by IDT. Primers were reconstituted in TE buffer to a stock concentration of 500μM. This is to minimise the number of freeze-thaw cycles that the primers undergo when being used. Dilutions were made to produce working primer stocks of 50μM or 10μM as required. To make 500μM stocks, Volume to add=(2x number of nMoles) μL Below is a table of sequences of all primers used in the USyd-Australia 2014 iGEM project, accompanied by a brief description of its application |
Name | Sequence (5'-3') | Theoretical Tm | Purpose |
---|---|---|---|
iGEM10 | AGCTTTCGCTAAGGATGATTTCTGGA | 58.2C | Screening and sequencing |
iGEM16 | GAGTGCCACCTGACGTCTAAGAAACC | 60.9C | For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM VF2 primer |
iGEM25 | CCCTGATTCTGTGGATAACCGTATTACCG | 60.0C | For BioBrick sequencing, amplification by PCR, or junction PCR. Alternative to iGEM VR primer |
iGEM1401 | GGGAAGCTTTCTTAGACGTCAGGTGGCACTTTTCGG | 66.3C | pBBR replicon |
iGEM1402 | TTTGGATCCTATGCTGCTGGCTACCCTGTGGAAC | 66.5C | pBBR replicon |
iGEM1403 | GTTCCACAGGGTAGCCAGCAGCATAGGATCCAAAGAGTGCCACCTGACGTCTAAGAAACC | 71.2C | primers for pSB prefix/suffix |
iGEM1404 | CCGAAAAGTGCCACCTGACGTCTAAGAAAGCTTCCCCCTGATTCTGTGGATAACCGTATTACCG | 70.3 | primers for pSB prefix/suffix |
iGEM1405 | GAGGTCGGACAGTATATTGAAACGTCAGGAGTCTAGATACCGAGGGACAGACTACCAACTCACA | primers for gene cassette circularisation (attC-aeBlue-aacC1) | |
iGEM1406 | GTATCTAGACTCCTGACGTTTCAATATACTGTCCGACCTCTTATTAGGTGGCGGTACTTGGGTCG | primers for gene cassette circularisation (attC-aeBlue-aacC1) | |
iGEM1407 | CTATATCTATGATCTCGCAGTCTCC | 53.8C | PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening |
iGEM1408 | GCCTTTTGCTCACATGTTCTTTC | 55.2C | PCR primers over the junction between aacC1 (G block) and pSB1C3 vector, for validation of successful G block insertion by PCR screening |
iGEM1409 | GTTTTTTTGGATGGAGTGAAACGATGGCGATTG | 61.7C | Amplification of iGEM-IntI1 gBlock forward primer |
iGEM1410 | TGACACCTTGCCCTTTTTTGCCG | 60.9C | Amplification of iGEM-IntI1 gBlock reverse primer |
iGEM1411 | GTTTTTTTGGATGGAGTGAAACGATGGCGATTG | 61.7C | Gblock primers for IntI1 in pSAM-R |
iGEM1412 | TGACACCTTGCCCTTTTTTG | 53.9C | Gblock primers for IntI1 in pSAM-R |
iGEM1413 | GACATTGCCGTCACTGCGTC | 59.1C | Junction primers for IntI1 in pSAM-R |
iGEM1414 | TGGTCCAGAACCTTGACCGAAC | 59.2C | Junction primers for IntI1 in pSAM-R |
iGEM1415 | AACCGAGGATGCGAACCACTTC | 59.7C | Junction primers for IntI1 in pSAM-R |
iGEM1416 | CCTTCAAACGTGCCGTAGAACAAGC | 60.4C | Junction primers for IntI1 in pSAM-R |
iGEM1417 | AAATACTAGTAGCGGCCGCTGCAGTCCGGCAAAAAAG | 67.6C | Linearisation of pSB1C3, containing full BioBrick prefix and suffix |
iGEM1418 | AAACTCTAGAAGCGGCCGCGAATTCCAGAAATCATCCTTAGC | 66.9C | Linearisation of pSB1C3, containing full BioBrick prefix and suffix |
iGEM1419 | TTTGAATTCGCGGCCGCTTCTAGAGTACCGAGGGACAGAC | 68.9C | Amplification of aeBlue gBlock. Forward primer. |
iGEM1420 | GGGCTGCAGCGGCCGCTACTAGTATTATTAGGTGG | 67.4C | Amplification of aeBlue gBlock. Reverse primer. |
iGEM1421 | GGGAATTCAAATCTAGAGACACCATCG | 57.1C | Amplification of LacI-Plac-AttI gBlock. Forward primer |
iGEM1422 | CCTGCAGTTTACTAGTTTTGCCTAACTTTGTTTTAG | 59.4C | Amplification of LacI-Plac-AttI gBlock. Reverse primer |
iGEM1423 | CAGGCTTTACACTTTATGCTTCCG | 56.3C | lacI-Plac-attI RHJ-F right hand junction forward primer (use with iGEM25) |
iGEM1424 | AATGTAATTCAGCTCCGCCATC | 55.5C | lacI-Plac-attI LHJ-R left hand junction reverse primer (use with iGEM16) |
iGEM1425 | AAATCTAGATGGCGCGGCTTAACTCAGGTGTTAGGCTTAGGAGGCTCAAGTATGGGCAT | 70.7C | For making aacC1 gene cassettes from Tn1696. Use with iGEM1426. |
iGEM1426 | AAAACTAGTGGCGTCGGCTTGGACGAATTGTTAGGCTTAGGTGGCGGTACTTGGGTC | 71.4C | For making aacC1 gene cassettes from Tn1696. Use with iGEM1425. |
iGEM1427 | TTTTCTAGAGTTTGATGTTATGGAGCAGCAACG | 60.2C | For making aacC1 gene cassettes from Tn1696. Use with iGEM1428. Alternative to iGEM1424. |
iGEM1428 | TTTACTAGTGCAAAAAGGCAGCAATTATGAGCC | 60.9C | For making aacC1 gene cassettes from Tn1696. Use with iGEM1427. Alternative to iGEM1426. |
NVC71 | CTAAGAATCCATAGTCCAACTCC | 52.4C | aadB gene, rvs primer for junction screen |
NVC92b | CACGCAAGACCTCAACCTTTTCC | 58.6C | aadB gene, rvs primer for junction screen |
NVC158 | GATACCTTGTGCGGCTATGTCTG | 57.6C | pUS41/44, left of cloning site |
NVC159 | GCCGCCTTGGGCCGGGTGATGTC | 69.2C | pUS41/44, right of cloning site |