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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
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cLS-F2 Resource Report Resource Website |
RRID:Addgene_32617 | rGH-PAL | Gallus gallus | Ampicillin | PMID:21060789 | Backbone Marker:Mark Emerson; Backbone Size:6610; Vector Backbone:Stagia3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 0 | ||
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pLKO.DEST.YFP Resource Report Resource Website |
RRID:Addgene_32683 | Chloramphenicol and Ampicillin | PMID:21418658 | The full plasmid sequence was assembled and may contain minor discrepancies that should not effect the function of the plasmid. | Backbone Size:7032; Vector Backbone:pLKO.1 puro; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Chloramphenicol and Ampicillin | 2026-09-19 02:17:10 | 0 | |||
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pCMV myc DAF-12(P687S) Resource Report Resource Website |
RRID:Addgene_32567 | DAF-12(P687S) | Caenorhabditis elegans | Ampicillin | PMID:21814518 | Vector Backbone:pCMV myc; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Proline 687 to Serine | 2026-09-19 02:17:09 | 0 | |
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pCAG:mRFP1 Resource Report Resource Website 1+ mentions |
RRID:Addgene_32600 | mRFP1 | Ampicillin | PMID:15996270 | The mRFP1 coding sequence was amplified by PCR using primers 5'RFP (5'-cgtagaattcgccaccaatggctagcatgactgg) and 3'RFP (5'-gcacgaattcgggcgccggtggagtggcggcc) using Pfx Polymerase (Invitrogen). The resulting product was cloned into the EcoRI site of pCAGGS to generate pCXmRFP1. Transient transfection of Cos-7 cells using Fugene 6 Transfection Reagent as per manufacturer's recommendations (Roche) was used to evaluate pCX-mRFP1, and verify that it produced robust red fluorescence More Information: https://www.ncbi.nlm.nih.gov/pubmed/12060735 A monomeric red fluorescent protein. Campbell et al (PNAS. 2002 Jun 11; 99:12) | Backbone Size:4700; Vector Backbone:pCAGGS; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 4 | ||
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pENTR.hU6hH1 Resource Report Resource Website |
RRID:Addgene_32686 | Kanamycin | PMID:21418658 | Backbone Marker:Invitrogen; Backbone Size:2720; Vector Backbone:pENTR4; Vector Types:Mammalian Expression, RNAi; Bacterial Resistance:Kanamycin | 2026-09-19 02:17:10 | 0 | ||||
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pCAG:GPI-GFP Resource Report Resource Website 10+ mentions |
RRID:Addgene_32601 | GPI-GFP | Ampicillin | PMID:16604528 | Backbone Size:4700; Vector Backbone:pCAGGS; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 13 | |||
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pTYF-G4BS-2TPH-EGFP-IRES-GAL4p65 Resource Report Resource Website |
RRID:Addgene_32569 | EGFP | Ampicillin | PMID:19212426 | This plasmid grows quite slowly. Please allow up to two days for growth. | Backbone Size:7469; Vector Backbone:pTYF; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 0 | ||
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pCAG:myr-Venus Resource Report Resource Website 1+ mentions |
RRID:Addgene_32602 | myr-Venus | Ampicillin | PMID:16604528 | To generate myristoylated fluorescent fusion proteins, an N-terminal myristoylation tag derived from Src was generated by adding the sequences MGSSKSKPK to the N-terminus of any given fluorescent protein. This was achieved by using the following oligonucleotide: 5′ GFP-MYR-Eco (5′-CTT GAA TTC GCC ACC ATG GGA AGC AGC AAG AGC AAG CCA AAG GTG AGC AAG GGC GAG GAG CTG). The GFP and Venus coding sequences were amplified from pEGFP-N1 (BD Biosciences, San Jose, CA) and pCS2-Venus (Nagai et al., 2002) to generate myr-GFP and myr-Venus, respectively, by high-fidelity polymerase chain reaction (PCR) using Pfx Polymerase (Invitrogen, La Jolla, CA) with the 5′ myristoylation primer combined with a 3′-GFP primer (5′-GTC ATG AAT TCT TAC TTG TAC AGC TCG TCC) primer, respectively. The resulting product was cloned into the EcoRI site of pCAGGS to generate pCX::myr-EGFP and pCX::myr-Venus | Backbone Size:4700; Vector Backbone:pCAGGS; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 5 | ||
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pISce1-D2EGFP Resource Report Resource Website |
RRID:Addgene_32674 | Ampicillin | Backbone Size:3500; Vector Backbone:pISce1; Vector Types:Zebrafish Transgenesis; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 0 | |||||
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pENTR-L5-Kir2.1-mCherry-L2 Resource Report Resource Website 1+ mentions |
RRID:Addgene_32669 | Kir2.1-mCherry | Mus musculus | Kanamycin | PMID:21772812 | Backbone Marker:Invitrogen; Vector Backbone:pDONR221 P5-P2; Vector Types:Gateway Cloning; Bacterial Resistance:Kanamycin | 2026-09-19 02:17:10 | 4 | ||
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pSADdeltaG-FLPo-DsRedX Resource Report Resource Website 1+ mentions |
RRID:Addgene_32650 | FLPo | Ampicillin | PMID:21867879 | Backbone Marker:Addgene plasmid 32634; Backbone Size:15428; Vector Backbone:pSADdeltaG; Vector Types:Mammalian Expression, Rabies virus; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 1 | |||
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pGEMTEZ-Kir2.1 Resource Report Resource Website 1+ mentions |
RRID:Addgene_32641 | Kir2.1 | Mus musculus | Ampicillin | PMID:15157418 | Addgene's sequencing results identified a single nucleotide insertion at bp#60/61 when compared to the author's sequence. The insert is upstream of the coding region and should not be a concern for the intended purpose of the plasmid. Silent mutations in Kir2.1 that do not affect the amino acid sequence were also found in Addgene's sequencing results. | Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 3 | |
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pTetO-Kir2.1-IRES-TLZ Resource Report Resource Website 1+ mentions |
RRID:Addgene_32642 | tetO-Kir2.1-IRES-TLZ | Mus musculus | Ampicillin | PMID:15157418 | Addgene's sequencing results identified a single nucleotide a single nucleotide deletion at bp#1135 when compared to the author's sequence. The insert is upstream of the coding region and should not be a concern for the intended purpose of the plasmid. Silent mutations in Kir2.1 that do not affect the amino acid sequence were also found in Addgene's sequencing results. | Backbone Marker:Stratagene; Vector Backbone:pBlueScript; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 1 | |
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pSADdeltaG-GFP-rtTA Resource Report Resource Website |
RRID:Addgene_32648 | GFP | Ampicillin | PMID:21867879 | Backbone Marker:Addgene plasmid 32634; Backbone Size:15428; Vector Backbone:pSADdeltaG; Vector Types:Mammalian Expression, Rabies virus; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 0 | |||
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pSADdeltaG-ChR2-mCherry Resource Report Resource Website 1+ mentions |
RRID:Addgene_32646 | ChR2 | Ampicillin | PMID:21867879 | Backbone Marker:Addgene plasmid 32634; Backbone Size:15428; Vector Backbone:pSADdeltaG; Vector Types:Mammalian Expression, Rabies virus; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 1 | |||
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pSADdeltaG-GFP-ER(T2)CreER(T2) Resource Report Resource Website 1+ mentions |
RRID:Addgene_32649 | GFP | Ampicillin | PMID:21867879 | Backbone Marker:Addgene plasmid 32634; Backbone Size:15428; Vector Backbone:pSADdeltaG; Vector Types:Mammalian Expression, Rabies virus; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 1 | |||
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pENTR-R4r-ECFP-R3r Resource Report Resource Website |
RRID:Addgene_32594 | ECFP | Kanamycin | PMID:21772812 | Backbone Marker:Invitrogen; Vector Backbone:pDONR221 P4r-P3r; Vector Types:Gateway Cloning; Bacterial Resistance:Kanamycin | 2026-09-19 02:17:09 | 0 | |||
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pCAG:H2B-EGFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_32599 | H2B-EGFP | Ampicillin | PMID:15619330 | Please note that the plasmid contains a duplication of the H2B-EGFP region as compared to the original depositor sequence. The depositor has confirmed that the plasmid functions as described in the associated publication. The coding sequence for the human histone H2B gene (X57127) was amplified from genomic DNA by PCR using Pfx Polymerase (Invitrogen). The resulting product was cloned into pCR4 TOPO (Invitrogen) to generate pH2B. The H2B fragment was then cloned into plasmids pEGFP-N1, pDsRed2-N1 pDsRedExpress-N1 (BD Biosciences, Inc) in order to generate plasmids pH2B-EGFP, pH2B-DsRed2 and pH2B-DsRedExpress (oligonucleotide sequences are available upon request). The resulting fusions were then re-amplified by PCR and cloned into the XhoI site of pCAGGS [19] to generate pCX-H2B-EGFP, pCX-H2B-DsRed2 and pCX-H2B-DsRedExpress. | Vector Backbone:pCAGGS; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 2 | ||
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pCAG:ECFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_32597 | ECFP | Ampicillin | PMID:12079497 | Backbone Size:4700; Vector Backbone:pCAGGS; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:09 | 1 | |||
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pcDNA-SADB19P Resource Report Resource Website 10+ mentions |
RRID:Addgene_32631 | SADB19P | Rabies virus | Ampicillin | PMID:21867879 | Backbone Marker:Invitrogen; Backbone Size:5428; Vector Backbone:pcDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-19 02:17:10 | 15 |
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