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pmscarlet i c1  (Addgene inc)


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    Structured Review

    Addgene inc pmscarlet i c1
    Pmscarlet I C1, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 103 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pmscarlet+c1/pmScarlet-i_C1+(Plasmid+%2385044)/pmc12992094-493-6-7
    Average 95 stars, based on 103 article reviews
    pmscarlet i c1 - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Cloning:

    Article Title: Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophy
    Article Snippet: .. USER cloning technology (NEB, Hitchin, UK) was used according to the manufacturer’s instructions to insert the EFEMP1 open reading frame excluding the stop codon into the mammalian expression vector p3xFLAG-CMV-14 (E7908) from Merck (Sigma-Aldrich, Gillingham, UK) and pmScarlet_C1 (Addgene, plasmid #85042), resulting in in-frame fusion of EFEMP1 with a C-terminal 3xFLAG tag (pEFEMP1-3xFLAG) and C-terminal mScarlet tag (pEFEMP1-mScarlet) respectively. .. The EFEMP1 c.1033C>T, p.Arg345Trp variant and a Kozak sequence upstream of the EFEMP1 open reading frame were introduced into pEFEMP1-mScarlet by site directed mutagenesis using the Q5 Site Directed Mutagenesis Kit (NEB) to generate pEFEMP1(R345W)-mScarlet.

    Expressing:

    Article Title: Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophy
    Article Snippet: .. USER cloning technology (NEB, Hitchin, UK) was used according to the manufacturer’s instructions to insert the EFEMP1 open reading frame excluding the stop codon into the mammalian expression vector p3xFLAG-CMV-14 (E7908) from Merck (Sigma-Aldrich, Gillingham, UK) and pmScarlet_C1 (Addgene, plasmid #85042), resulting in in-frame fusion of EFEMP1 with a C-terminal 3xFLAG tag (pEFEMP1-3xFLAG) and C-terminal mScarlet tag (pEFEMP1-mScarlet) respectively. .. The EFEMP1 c.1033C>T, p.Arg345Trp variant and a Kozak sequence upstream of the EFEMP1 open reading frame were introduced into pEFEMP1-mScarlet by site directed mutagenesis using the Q5 Site Directed Mutagenesis Kit (NEB) to generate pEFEMP1(R345W)-mScarlet.

    Plasmid Preparation:

    Article Title: Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophy
    Article Snippet: .. USER cloning technology (NEB, Hitchin, UK) was used according to the manufacturer’s instructions to insert the EFEMP1 open reading frame excluding the stop codon into the mammalian expression vector p3xFLAG-CMV-14 (E7908) from Merck (Sigma-Aldrich, Gillingham, UK) and pmScarlet_C1 (Addgene, plasmid #85042), resulting in in-frame fusion of EFEMP1 with a C-terminal 3xFLAG tag (pEFEMP1-3xFLAG) and C-terminal mScarlet tag (pEFEMP1-mScarlet) respectively. .. The EFEMP1 c.1033C>T, p.Arg345Trp variant and a Kozak sequence upstream of the EFEMP1 open reading frame were introduced into pEFEMP1-mScarlet by site directed mutagenesis using the Q5 Site Directed Mutagenesis Kit (NEB) to generate pEFEMP1(R345W)-mScarlet.

    Transfection:

    Article Title: Cyclin-dependent kinase-like 5 (CDKL5) binds to talin and is anchored at the postsynaptic density via direct interaction with PDZ domains
    Article Snippet: At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations. .. The plasmids used for transfections were as follows: PSD-95-pTagRFP (Addgene, #52671), pmScarlet_C1 (Addgene, #85042), pEGFP-N1 (a gift from Pirta Hotulainen, University of Helsinki), and the CDKL5 cloned constructs GFP-CDKL5, GFP-CDKL5 L960D, or CDKL5-GFP. .. At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations.

    Clone Assay:

    Article Title: Cyclin-dependent kinase-like 5 (CDKL5) binds to talin and is anchored at the postsynaptic density via direct interaction with PDZ domains
    Article Snippet: At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations. .. The plasmids used for transfections were as follows: PSD-95-pTagRFP (Addgene, #52671), pmScarlet_C1 (Addgene, #85042), pEGFP-N1 (a gift from Pirta Hotulainen, University of Helsinki), and the CDKL5 cloned constructs GFP-CDKL5, GFP-CDKL5 L960D, or CDKL5-GFP. .. At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations.

    Construct:

    Article Title: Cyclin-dependent kinase-like 5 (CDKL5) binds to talin and is anchored at the postsynaptic density via direct interaction with PDZ domains
    Article Snippet: At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations. .. The plasmids used for transfections were as follows: PSD-95-pTagRFP (Addgene, #52671), pmScarlet_C1 (Addgene, #85042), pEGFP-N1 (a gift from Pirta Hotulainen, University of Helsinki), and the CDKL5 cloned constructs GFP-CDKL5, GFP-CDKL5 L960D, or CDKL5-GFP. .. At DIV14, 100,000 cortical neurons per coverslip were transfected with 2 μL of Lipofectamine 2000 (ThermoFisher) and 1.2 μg of DNA following the manufacturer’s recommendations.

    Polymerase Chain Reaction:

    Article Title: Synthetic multicolor antigen-stabilizable nanobody platform for intersectional labelling and functional imaging
    Article Snippet: VIS-Fbs to GFP with insertions of mTagBFP2, mTFP1, mWasabi, mNeonGreen, mOrange, LSSmOrange, CyOFP1, mScarlet-I, mScarlet, LSSmScarlet, mNeptune2, mCardinal, PAmCherry or mEos4a were designed by swapping miRFP670nano3 gene with FPs genes in the NIR-Fb plasmid (Addgene no.184675) by NEBuilder HiFi DNA Assembly Kit. .. All oligonucleotide primers for PCR amplification were purchased from Thermo Fisher Scientific ( Supplementary Table 1 ). mTagBFP2, mTFP1, mWasabi, mNeonGreen, mOrange, LSSmOrange, CyOFP1, mScarlet-I, mScarlet, LSSmScarlet, mNeptune2, mCardinal, PAmCherry, and mEos4a were amplified from pBAD-mTagBFP2 (Addgene no.34632), pBAD-mTFP1 (Addgene no.54553), pmWasabi-FAK-5 (Addgene no.56502), pmOrange-N1 (Addgene no.54499), pBAD-LSSmOrange (Addgene no.37129), pKK-CyOFP1-TEV (Addgene no.105782), pmScarlet-I-C1 (Addgene no.85044), pmScarlet-C1 (Addgene no.85042), pcDNA3-mNeptune2 (Addgene no.51309), pcDNA3-mCardinal (Addgene no.51311), PAmCherry1-C1 (Addgene no.54495) and mEoa4a-N1 (Addgene no.54811) plasmids, respectively. .. To generate the NES-mTagBFP2-Fb plasmid, the mTagBFP2-Fb GFP gene was swapped with DEVD-mCardinal-3xNLS construct in the pcDNA-NES-DEVD-mCardinal-3xNLS plasmid (Addgene no.164052) at the BamHI/XhoI sites.

    Amplification:

    Article Title: Synthetic multicolor antigen-stabilizable nanobody platform for intersectional labelling and functional imaging
    Article Snippet: VIS-Fbs to GFP with insertions of mTagBFP2, mTFP1, mWasabi, mNeonGreen, mOrange, LSSmOrange, CyOFP1, mScarlet-I, mScarlet, LSSmScarlet, mNeptune2, mCardinal, PAmCherry or mEos4a were designed by swapping miRFP670nano3 gene with FPs genes in the NIR-Fb plasmid (Addgene no.184675) by NEBuilder HiFi DNA Assembly Kit. .. All oligonucleotide primers for PCR amplification were purchased from Thermo Fisher Scientific ( Supplementary Table 1 ). mTagBFP2, mTFP1, mWasabi, mNeonGreen, mOrange, LSSmOrange, CyOFP1, mScarlet-I, mScarlet, LSSmScarlet, mNeptune2, mCardinal, PAmCherry, and mEos4a were amplified from pBAD-mTagBFP2 (Addgene no.34632), pBAD-mTFP1 (Addgene no.54553), pmWasabi-FAK-5 (Addgene no.56502), pmOrange-N1 (Addgene no.54499), pBAD-LSSmOrange (Addgene no.37129), pKK-CyOFP1-TEV (Addgene no.105782), pmScarlet-I-C1 (Addgene no.85044), pmScarlet-C1 (Addgene no.85042), pcDNA3-mNeptune2 (Addgene no.51309), pcDNA3-mCardinal (Addgene no.51311), PAmCherry1-C1 (Addgene no.54495) and mEoa4a-N1 (Addgene no.54811) plasmids, respectively. .. To generate the NES-mTagBFP2-Fb plasmid, the mTagBFP2-Fb GFP gene was swapped with DEVD-mCardinal-3xNLS construct in the pcDNA-NES-DEVD-mCardinal-3xNLS plasmid (Addgene no.164052) at the BamHI/XhoI sites.



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    Addgene inc mscarlet
    a Live imaging showing expression of <t>AP2-G.mScarlet</t> (mSc) in a schizont stage parasite from mutated ( 3D7.stk2 Δ //ap2-g.L . mSc : bottom panel) or mutation corrected ( 3D7.stk2 Δ //ap2-g.V . mSc : top panel) lines that were stained with Hoechst to detect DNA. b Live imaging of double reporter lines showing AP2-G and MSRP1 expression in the mutation corrected line ( 3D7.stk2 Δ //ap2-g.V . <t>mSc//msrp1.</t> <t>mNeonGreen</t> (mNG) : top panel), not the mutated line ( 3D7.stk2 Δ //ap2-g.L . mSc//msrp1.mNG : bottom panel). Both parasite lines were stained with Hoechst to detect DNA. The images are representative of the 100 parasite positive red blood cells analyzed. c Quantification of AP2-G.mSc and MSRP1.mNG positive schizonts in the mutated (left panel) and mutation corrected (right panel) lines shown in ( b ). d Retro analysis of flow cytometer data shows AP2.G.mSc positive schizonts (top panel) have less Hoechst staining, consistent with younger schizonts with less DNA, whereas schizonts positive for both AP2.G.mSc and MSRP1.mNG (bottom panel) have higher Hoechst staining suggesting they are older. e Flow cytometric quantification of single positive (AP2-G.mSc + /MSRP1mNG-: dotted line) or double positive (AP2-G.mSc + /MSRP1.mNG + : continuous line) schizonts from 37 to 46 hpi using 3D7.stk2 Δ //ap2-g.V . mSc//msrp1.mNG parasites. Details of flow cytometric quantification are provided as Supplementary Fig. . Source data are provided as a Source Data file.
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    Image Search Results


    a Live imaging showing expression of AP2-G.mScarlet (mSc) in a schizont stage parasite from mutated ( 3D7.stk2 Δ //ap2-g.L . mSc : bottom panel) or mutation corrected ( 3D7.stk2 Δ //ap2-g.V . mSc : top panel) lines that were stained with Hoechst to detect DNA. b Live imaging of double reporter lines showing AP2-G and MSRP1 expression in the mutation corrected line ( 3D7.stk2 Δ //ap2-g.V . mSc//msrp1. mNeonGreen (mNG) : top panel), not the mutated line ( 3D7.stk2 Δ //ap2-g.L . mSc//msrp1.mNG : bottom panel). Both parasite lines were stained with Hoechst to detect DNA. The images are representative of the 100 parasite positive red blood cells analyzed. c Quantification of AP2-G.mSc and MSRP1.mNG positive schizonts in the mutated (left panel) and mutation corrected (right panel) lines shown in ( b ). d Retro analysis of flow cytometer data shows AP2.G.mSc positive schizonts (top panel) have less Hoechst staining, consistent with younger schizonts with less DNA, whereas schizonts positive for both AP2.G.mSc and MSRP1.mNG (bottom panel) have higher Hoechst staining suggesting they are older. e Flow cytometric quantification of single positive (AP2-G.mSc + /MSRP1mNG-: dotted line) or double positive (AP2-G.mSc + /MSRP1.mNG + : continuous line) schizonts from 37 to 46 hpi using 3D7.stk2 Δ //ap2-g.V . mSc//msrp1.mNG parasites. Details of flow cytometric quantification are provided as Supplementary Fig. . Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: A single valine to leucine switch disrupts Plasmodium falciparum AP2-G DNA binding and reveals GDV1’s role in ap2-g activation

    doi: 10.1038/s41467-026-68416-1

    Figure Lengend Snippet: a Live imaging showing expression of AP2-G.mScarlet (mSc) in a schizont stage parasite from mutated ( 3D7.stk2 Δ //ap2-g.L . mSc : bottom panel) or mutation corrected ( 3D7.stk2 Δ //ap2-g.V . mSc : top panel) lines that were stained with Hoechst to detect DNA. b Live imaging of double reporter lines showing AP2-G and MSRP1 expression in the mutation corrected line ( 3D7.stk2 Δ //ap2-g.V . mSc//msrp1. mNeonGreen (mNG) : top panel), not the mutated line ( 3D7.stk2 Δ //ap2-g.L . mSc//msrp1.mNG : bottom panel). Both parasite lines were stained with Hoechst to detect DNA. The images are representative of the 100 parasite positive red blood cells analyzed. c Quantification of AP2-G.mSc and MSRP1.mNG positive schizonts in the mutated (left panel) and mutation corrected (right panel) lines shown in ( b ). d Retro analysis of flow cytometer data shows AP2.G.mSc positive schizonts (top panel) have less Hoechst staining, consistent with younger schizonts with less DNA, whereas schizonts positive for both AP2.G.mSc and MSRP1.mNG (bottom panel) have higher Hoechst staining suggesting they are older. e Flow cytometric quantification of single positive (AP2-G.mSc + /MSRP1mNG-: dotted line) or double positive (AP2-G.mSc + /MSRP1.mNG + : continuous line) schizonts from 37 to 46 hpi using 3D7.stk2 Δ //ap2-g.V . mSc//msrp1.mNG parasites. Details of flow cytometric quantification are provided as Supplementary Fig. . Source data are provided as a Source Data file.

    Article Snippet: Plasmid with tdTomato (pGEMT-PT2A-iRFP670-Tdtomato-GFP: Addgene plasmid # 111817) or mScarlet (pmScarlet_C1: Addgene plasmid # 85042) or mNeonGreen (ER-mNeonGreen: Addgene plasmid # 137804) or NanoLuciferease (pUAS-NanoLuc: Addgene plasmid # 87696) were obtained from Addgene Inc (USA).

    Techniques: Imaging, Expressing, Mutagenesis, Staining, Flow Cytometry