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Species: Homo sapiens
Genetic Insert: hCXCR4
Vector Backbone Description: Vector Backbone:mTFP1-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:37591879
Proper citation: RRID:Addgene_110196 Copy
Species: Homo sapiens
Genetic Insert: EGFR D837A
Vector Backbone Description: Backbone Size:5169; Vector Backbone:pBABE puro; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:16187797
Comments: Author has deposited the sequence of the insert to Addgene. Click on "sequence" to view. Point mutation made by using the following primers to PCR from plasmid 11011: 5'-GGTGCACCGCGCCCTGGCAGCCA-3' and 5'-TGGCTGCCAGGGCGCGGTGCACC-3'
Proper citation: RRID:Addgene_11014 Copy
Species: Homo sapiens
Genetic Insert: hCCR5
Vector Backbone Description: Vector Backbone:LSSmOrange-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:37591879
Proper citation: RRID:Addgene_110194 Copy
Species: Homo sapiens
Genetic Insert: fibroblast growth factor receptor 2
Vector Backbone Description: Backbone Marker:Sigma; Backbone Size:6300; Vector Backbone:p3xFlag-CMV-13; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_110110 Copy
Genetic Insert: Firefly luciferase
Vector Backbone Description: Vector Backbone:Hy_pMT dati MCS Exon; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:29773557
Proper citation: RRID:Addgene_110115 Copy
Species: Drosophila melanogaster
Genetic Insert: dati
Vector Backbone Description: Vector Backbone:Hy_pMT; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:29773557
Comments: Depositor notes discrepancies found in Addgene QC sequence are not of functional concern
Proper citation: RRID:Addgene_110119 Copy
Species: Rattus norvegicus
Genetic Insert: PTEN
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:4731; Vector Backbone:pEGFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:20628354
Proper citation: RRID:Addgene_110182 Copy
Species: Roseburia inulinivorans strain A2-194
Genetic Insert: Propanediol Dehydratase Activating Enzyme
Vector Backbone Description: Backbone Marker:EMD Biosciences; Backbone Size:5292; Vector Backbone:pET-28 a (+); Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:28183913
Proper citation: RRID:Addgene_110180 Copy
Species: Mus musculus
Genetic Insert: MeCP2_e2 FL [R111G] (mouse cDNA)
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:4680; Vector Backbone:pEGFP-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:29019980
Proper citation: RRID:Addgene_110187 Copy
Species: Homo sapiens
Genetic Insert: fibroblast growth factor receptor 2
Vector Backbone Description: Backbone Marker:Sigma; Backbone Size:6300; Vector Backbone:p3xFlag-CMV-13; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30761385
Proper citation: RRID:Addgene_110105 Copy
Species: Homo sapiens
Genetic Insert: fibroblast growth factor receptor 2
Vector Backbone Description: Backbone Marker:Sigma; Backbone Size:6300; Vector Backbone:p3xFlag-CMV-13; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_110106 Copy
Species: Other
Genetic Insert: scaffold Sybody of the convex library
Vector Backbone Description: Vector Backbone:pBXPHM3; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:29792401
Proper citation: RRID:Addgene_110104 Copy
Species: Homo sapiens
Genetic Insert: fibroblast growth factor receptor 2
Vector Backbone Description: Backbone Marker:Sigma; Backbone Size:6300; Vector Backbone:p3xFlag-CMV-13; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_110107 Copy
Species: Homo sapiens
Genetic Insert: fibroblast growth factor receptor 2
Vector Backbone Description: Backbone Marker:Sigma; Backbone Size:6300; Vector Backbone:p3xFlag-CMV-13; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_110108 Copy
Species: Clostridium difficile 70-100-2010
Genetic Insert: Pyrroline-5-carboxylate Reductase
Vector Backbone Description: Backbone Marker:EMD Biosciences; Backbone Size:5292; Vector Backbone:pET-28 a (+); Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:28183913
Proper citation: RRID:Addgene_110295 Copy
Species: Mus musculus
Genetic Insert: mcry1 K31R
Vector Backbone Description: Backbone Marker:genscript; Vector Backbone:pCDNA 3.1 HA tag; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:23452855
Proper citation: RRID:Addgene_110297 Copy
Species: A. victoria
Genetic Insert: eGFPemerald
Vector Backbone Description: Backbone Marker:Unknown; Backbone Size:2700; Vector Backbone:pUC18; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:11771662
Comments: GFPemerald purchased from Packard.
Proper citation: RRID:Addgene_110210 Copy
Species: Homo sapiens
Genetic Insert: SPRTN
Vector Backbone Description: Backbone Marker:Invitrogen; Vector Backbone:pCDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:25261934
Comments: According to the large datasets deposited in various databses like: dbSNP, 1000 Genomes, the ExAC and the gnomAD browser, the variant c.887C>T, p.Pro296Leu is found roughly in 50% of general world population. Moreover, according to the large-scale sequencing studies involving more than 135 000 healthy individuals deposited in The Genome Aggregation Database (gnomAD), it is more prevalent than the previously assigned reference allele in the European population, with a minor allele frequency of 0.69: http://gnomad.broadinstitute.org/variant/1-231488524-C-T
Taken this into account, this variant (P296L) is s actually the accurate reference (wild-type) allele, and thus this variant can not be the cause of any Mendelian disease. This is the reason why all our vectors bear this variant.
Proper citation: RRID:Addgene_110215 Copy
Species: Homo sapiens
Genetic Insert: SPRTN
Vector Backbone Description: Backbone Marker:Invitrogen; Vector Backbone:pCDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:27871366
Comments: According to the large datasets deposited in various databses like: dbSNP, 1000 Genomes, the ExAC and the gnomAD browser, the variant c.887C>T, p.Pro296Leu is found roughly in 50% of general world population. Moreover, according to the large-scale sequencing studies involving more than 135 000 healthy individuals deposited in The Genome Aggregation Database (gnomAD), it is more prevalent than the previously assigned reference allele in the European population, with a minor allele frequency of 0.69: http://gnomad.broadinstitute.org/variant/1-231488524-C-T
Taken this into account, this variant (P296L) is s actually the accurate reference (wild-type) allele, and thus this variant can not be the cause of any Mendelian disease. This is the reason why all our vectors bear this variant.
Proper citation: RRID:Addgene_110216 Copy
Species: Homo sapiens
Genetic Insert: SPRTN
Vector Backbone Description: Backbone Marker:Invitrogen; Vector Backbone:pCDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:25261934
Comments: According to the large datasets deposited in various databses like: dbSNP, 1000 Genomes, the ExAC and the gnomAD browser, the variant c.887C>T, p.Pro296Leu is found roughly in 50% of general world population. Moreover, according to the large-scale sequencing studies involving more than 135 000 healthy individuals deposited in The Genome Aggregation Database (gnomAD), it is more prevalent than the previously assigned reference allele in the European population, with a minor allele frequency of 0.69: http://gnomad.broadinstitute.org/variant/1-231488524-C-T
Taken this into account, this variant (P296L) is s actually the accurate reference (wild-type) allele, and thus this variant can not be the cause of any Mendelian disease. This is the reason why all our vectors bear this variant.
Proper citation: RRID:Addgene_110214 Copy
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