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http://www.addgene.org/41108

Species: Drosophila melanogaster
Genetic Insert: Loquacious-PA
Vector Backbone Description: Backbone Size:8000; Vector Backbone:pattB; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41108 Copy   

•   Source: Addgene

http://www.addgene.org/41107

Species: Synthetic
Genetic Insert: taranismutant3'UTR
Vector Backbone Description: Backbone Size:6000; Vector Backbone:siCheck2; Vector Types:Luciferase; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41107 Copy   

•   Source: Addgene

http://www.addgene.org/41106

Species: Synthetic
Genetic Insert: taranis3'UTR
Vector Backbone Description: Backbone Size:6000; Vector Backbone:siCheck2; Vector Types:Luciferase; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41106 Copy   

•   Source: Addgene

http://www.addgene.org/41104

Species: Synthetic
Genetic Insert: Gk3'UTR
Vector Backbone Description: Backbone Size:6000; Vector Backbone:siCheck2; Vector Types:Luciferase; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41104 Copy   

•   Source: Addgene

http://www.addgene.org/41103

Species: Synthetic
Genetic Insert: 8xmiR307_21nt-seedonly
Vector Backbone Description: Backbone Size:6000; Vector Backbone:siCheck2; Vector Types:Luciferase; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41103 Copy   

•   Source: Addgene

http://www.addgene.org/41069

Species: Homo sapiens
Genetic Insert: Tetherin
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:7162; Vector Backbone:pQCXIP; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:20140192
Comments: This is a viral-delivery-compatible HA.Tetherin expression construct. It was generated by cloning of tetherin from plasmid pCMV-HA.Tetherin (Addgene plasmid #41068) into AgeI and PacI restriction sites of pQCXIP (Clontech).

Proper citation: RRID:Addgene_41069 Copy   

•   Source: Addgene

http://www.addgene.org/41067

Vector Backbone Description: Backbone Size:3726; Vector Backbone:pTKIP; Vector Types:; Bacterial Resistance:Ampicillin
Defining Citation: PMID:20047970

Proper citation: RRID:Addgene_41067 Copy   

•   Source: Addgene

http://www.addgene.org/41100

Species: Synthetic
Genetic Insert: 4xmiR307_23nt-seedonly
Vector Backbone Description: Backbone Size:6000; Vector Backbone:siCheck2; Vector Types:Luciferase; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23063653

Proper citation: RRID:Addgene_41100 Copy   

•   Source: Addgene

http://www.addgene.org/41065

Vector Backbone Description: Backbone Size:4146; Vector Backbone:pTKIP; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol and Ampicillin
Defining Citation: PMID:20047970

Proper citation: RRID:Addgene_41065 Copy   

•   Source: Addgene

http://www.addgene.org/41209

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-bsx-Right
Vector Backbone Description: Backbone Marker:Addgene plasmid #32287; Backbone Size:6447; Vector Backbone:JDS71; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TATCTCTGGATCTCGAAC It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41209 Copy   

•   Source: Addgene

http://www.addgene.org/41206

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-bmp10-Left
Vector Backbone Description: Backbone Marker:Addgene plasmid #32287; Backbone Size:6447; Vector Backbone:JDS71; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TCAGCTCCCCGGAGAGGC It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41206 Copy   

•   Source: Addgene

http://www.addgene.org/41205

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-bbc3-(puma)-Right
Vector Backbone Description: Backbone Marker:Addgene plasmid #32288; Backbone Size:6447; Vector Backbone:JDS74; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TGGCCAGGCGTCCTGACG It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41205 Copy   

•   Source: Addgene

http://www.addgene.org/41203

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-avpr1b-Right
Vector Backbone Description: Backbone Marker:Addgene plasmid #32287; Backbone Size:6447; Vector Backbone:JDS71; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TTGGCCACATCTTCGTTC It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41203 Copy   

•   Source: Addgene

http://www.addgene.org/41161

Species: Homo sapiens
Genetic Insert: PBD HK-AA
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5500; Vector Backbone:pcDNA3.1/3x myc-C; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:16267267
Comments: Addgene plasmid #41162: Plk1-PBDWT (aa 326–603) was cloned in-frame by PCR into a pcDNA3.1 vector encoding an amino-terminal 3xmyc-tag (Invitrogen, Carlsbad, CA) using primers 5
'-CCG GAA TTC CAG ATC TTC GAT TGC TCC CAG CAG CCT GG-3
' and 5
'-CCG CTC GAG TTA GGA GGC CTT GAG ACG GTT GC-3
'. The Plk1-PBDAA mutant (H538A, K540A) was made by site-directed mutagenesis using the following primers: 5'
-CAA TTC TCC GGA GCC CCG CCT ATC TGT CCC-3
' and 5
'-GGG ACA GAT AGG CGG GGC TCC GGA GAA TTG-3
'.

Proper citation: RRID:Addgene_41161 Copy   

•   Source: Addgene

http://www.addgene.org/41160

Species: Homo sapiens
Genetic Insert: Plk1
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5527; Vector Backbone:pRc/CMV; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:7962193
Comments: cDNA fragments spanning parts of the catalytic domains of human protein kinases were amplified by PCR, as described by Schultz and Nigg (1993). A 144 bp fragment (named HsPK28) showing 88% nucleotide identity to Drosophila polo was used to probe a λgt 10 library prepared from a human nasopharyngeal carcinoma (Hitt et al., 1989). Approximately 500,000 plaques were screened by plaque hybridization (Sambrook et al., 1989), and 17 phage showing strong hybridization were purified. DNA was prepared using Lambdasorb (Promega Biotech, Madison, WI). One plasmid (referred to as Plk1-pGEM) with a 2143 bp insert contained the entire coding sequence for a protein kinase closely related to Drosophila polo. This insert was sequenced on both strands by the method of Chen and Seeburg (1985), using the Sequenase kit (United States Biochemicals). To express a full-length Plk1 protein, the 1998 bp fragment of Plk1-pGEM was introduced into the pRc/CMV vector (Invitrogen Corporation, San Diego), to create Plk1-CMV. An N-terminally myc-tagged Plk1-CMV was also constructed. In the resulting mycplk1 protein, the N terminus of Plk1 is extended by the oligopeptide MEQKLISEEDLNMNSCSPGS (Evan et al., 1985).

Proper citation: RRID:Addgene_41160 Copy   

•   Source: Addgene

http://www.addgene.org/41202

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-avpr1b-Left
Vector Backbone Description: Backbone Marker:Addgene plasmid #32285; Backbone Size:6447; Vector Backbone:JDS70; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TCACGGCGAACAACACTA It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41202 Copy   

•   Source: Addgene

http://www.addgene.org/41200

Species: Danio rerio
Genetic Insert: ZebrafishCommunity-arap3a-Left
Vector Backbone Description: Backbone Marker:Addgene plasmid #32290; Backbone Size:6447; Vector Backbone:JDS78; Vector Types:Mammalian Expression, T7; Bacterial Resistance:Ampicillin
Defining Citation: PMID:21822241
Comments: Target binding site: TGGCAACAATCGGTCCGT It is strongly recommended that users perform a diagnostic digest to verify this plasmid prior to use. For example, a double digest of the plasmid with BamHI and KpnI should result in two bands at 2.3kb and 5.8kb.

Proper citation: RRID:Addgene_41200 Copy   

•   Source: Addgene

http://www.addgene.org/41166

Species: Homo sapiens
Genetic Insert: Rootletin
Vector Backbone Description: Backbone Marker:Modified from Clontech; Backbone Size:4700; Vector Backbone:pCJW201 (modified pEGFP-C1); Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:16203858
Comments: The partial cDNA clones KIAA0445 (Kazusa DNA Research Institute) and IMAGE clone 6150861 (Deutsches Ressourcenzentrum fuer Genomforschung GmbH) were fused, and the complete coding sequence for rootletin was cloned into pBluescript II SK- (Addgene plasmid #41168) and subsequently subcloned into pEGFP-C1 (CLONTECH Laboratories, Inc.). All constructs were confirmed by sequencing.

Proper citation: RRID:Addgene_41166 Copy   

•   Source: Addgene

http://www.addgene.org/41163

Species: Homo sapiens
Genetic Insert: PICH
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:4700; Vector Backbone:pEGFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:17218258
Comments: The complete ORF of PICH (corresponding exactly to FLJ20105; Acc. No. BC111486) was amplified by nested PCR, using a HeLa Marathon library (Clontech laboratories Inc.), and cloned into pEGFP-C1 vector (Clontech laboratories Inc.). The following primer pairs were used: primer pair 1: AAG CTC CAG CTC CAA GCT CC and TGC TTT TTG AGA TCT TTC TTG CC, primer pair 2: GACTCGAGCTATGGAGGCATCCCGAAGGTTTC and GCCCGGGTCAATTGTTATTAAGTTGC. These primers contain Xho1 and Xma1 sites, respectively, used for cloning.

Proper citation: RRID:Addgene_41163 Copy   

•   Source: Addgene

http://www.addgene.org/41152

Species: Homo sapiens
Genetic Insert: Cep215
Vector Backbone Description: Backbone Marker:Modified from Clontech; Backbone Size:4110; Vector Backbone:pCJW206 (modified pEGFP-C1); Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:18042621
Comments: The Cep215 cDNA sequence was obtained from KIAA1633 clone (from Kazusa DNA Research Institute). Using PCR, a frameshift within the sequence was corrected and missing 5' coding information was obtained by PCR amplification from Marathon cDNA library (Clontech). Constructs were fused to yield the complete coding sequence of Cep215, and subcloned into a mammalian expression vector providing a Myc epitope-tag. All constructs were confirmed by sequencing.

Proper citation: RRID:Addgene_41152 Copy   

•   Source: Addgene