BBa_K2100001 1 BBa_K2100001 pENTR pEREx5 2016-09-25T11:00:00Z 2016-09-26T05:07:50Z No, this a part synthesized by IDT. TBD. false false _2568_ 31606 31606 9 false Like TRE (ELABORATE HERE) false Kathleen Brandes annotation2485067 1 ERE site range2485067 1 107 118 annotation2485068 1 ERE site range2485068 1 140 151 annotation2485066 1 ERE site range2485066 1 67 78 annotation2485070 1 minCMV range2485070 1 204 259 annotation2485065 1 ERE site range2485065 1 33 44 annotation2485069 1 ERE site range2485069 1 173 184 BBa_K2100043 1 BBa_K2100043 pEXPR pERE5:BM3R1 2016-10-16T11:00:00Z 2016-10-17T07:41:46Z This is a synthetic promoter with a gene from the mammalian genome. description here. false false _2568_ 31606 31606 9 false This composite part expression vector was created by an LR reaction via gateway cloning. It is a promoter (flanked by L4, R1 sites) and a gene (flanked by L1, L2 sites) cloned into a backbone that has a negative selection marker between R4 and R2 sites. This part adheres to RFC 65 for recombination based cloning of mammalian parts. false Kathleen Brandes component2516099 1 BBa_K2100018 component2516098 1 BBa_K2100001 annotation2516098 1 BBa_K2100001 range2516098 1 1 289 annotation2516099 1 BBa_K2100018 range2516099 1 298 933 BBa_K2100018 1 BBa_K2100018 pENTR BM3R1 2016-10-13T11:00:00Z 2016-10-14T04:48:06Z This is from a mammalian genome. description here. false false _2568_ 31606 31606 9 false This basic part entry vector is flanked by L1 and L2 sites, which are used to denote a gene. This can be cascade with a promoter (flanked by L4, R1 sites) using an LR reaction and cloning into a cloned into a backbone that has a negative selection marker between R4 and R2 sites. This part adheres to RFC 65 for recombination based cloning of mammalian parts. false Kathleen Brandes BBa_K2100018_sequence 1 gctgagccaccatggaaagcacccccaccaagcagaaggccatcttcagcgccagcctgctgctgttcgccgagagaggctttgacgccaccaccatgcccatgattgccgagaacgccaaagtgggagccggcaccatctaccggtacttcaagaacaaagagagcctggtcaacgagctgttccagcagcacgtgaacgagtttctgcagtgcatcgagagcggcctggccaatgagagggacggctacagagatggcttccaccacatcttcgagggcatggtcaccttcaccaagaaccaccccagagccctgggcttcatcaagacccacagccagggcacctttctgaccgaggaaagccggctggcctaccagaaactggtggaattcgtgtgcaccttcttcagagagggccagaaacagggcgtgatccggaacctgcccgagaatgccctgatcgccatcctgttcggcagcttcatggaagtgtacgagatgatcgagaacgactacctgagcctgaccgacgagctgctgaccggcgtggaagaatctctgtgggccgctctgagcagacagagcgccagcccccccaagaaaaagcggaaagtgtgatgagctagctgatacc BBa_K2100043_sequence 1 gctccgaattcgacgatgtcgagtttactcctatggtcaaaatgaccacgtatgtcgagtttactaacgcggtcacattgaccacgtatgtcgagtttactttgtaggtcaggctgaccacgtatgtcgagtttattttgcggtcagtatgaccacgtatgtcgagtttactttgacggtcatattgaccacgtatgtcgaggtaggcgtgtacggtgggaggcctatataagcagagctcgtttagtgaaccgtcagatcgcaaagggcgaattcgaccgaattcgactactagaggctgagccaccatggaaagcacccccaccaagcagaaggccatcttcagcgccagcctgctgctgttcgccgagagaggctttgacgccaccaccatgcccatgattgccgagaacgccaaagtgggagccggcaccatctaccggtacttcaagaacaaagagagcctggtcaacgagctgttccagcagcacgtgaacgagtttctgcagtgcatcgagagcggcctggccaatgagagggacggctacagagatggcttccaccacatcttcgagggcatggtcaccttcaccaagaaccaccccagagccctgggcttcatcaagacccacagccagggcacctttctgaccgaggaaagccggctggcctaccagaaactggtggaattcgtgtgcaccttcttcagagagggccagaaacagggcgtgatccggaacctgcccgagaatgccctgatcgccatcctgttcggcagcttcatggaagtgtacgagatgatcgagaacgactacctgagcctgaccgacgagctgctgaccggcgtggaagaatctctgtgggccgctctgagcagacagagcgccagcccccccaagaaaaagcggaaagtgtgatgagctagctgatacc BBa_K2100001_sequence 1 gctccgaattcgacgatgtcgagtttactcctatggtcaaaatgaccacgtatgtcgagtttactaacgcggtcacattgaccacgtatgtcgagtttactttgtaggtcaggctgaccacgtatgtcgagtttattttgcggtcagtatgaccacgtatgtcgagtttactttgacggtcatattgaccacgtatgtcgaggtaggcgtgtacggtgggaggcctatataagcagagctcgtttagtgaaccgtcagatcgcaaagggcgaattcgaccgaattcgac igem2sbol 1 iGEM to SBOL conversion Conversion of the iGEM parts registry to SBOL2.1 Chris J. Myers James Alastair McLaughlin 2017-03-06T15:00:00.000Z