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pegfp c1 vector  (TaKaRa)


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    TaKaRa pegfp c1 vector
    Pegfp C1 Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 3285 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pegfp+c1+vector/pmCherry-C1+Vector/bio_rxiv__2025__11__26__690680-258-17-19
    Average 96 stars, based on 3285 article reviews
    pegfp c1 vector - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1
    Article Snippet: .. Resistant EGFP-SHKBP1 or 2xUBA-3xFLAG-SHKBP1 (2US) or GFP-SHKBP1 (F44A) were subcloned into the pCDH-CMV-MCS vector to yield the lentiviral plasmid. p62-related constructs were amplified from HA-p62, Addgene (28027), which was subcloned into pEGFP-C1 vector (Clontech) using EcoRI and KpnI to generate GFP-p62. ..

    Article Title: Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis.
    Article Snippet: Plasmids pGEX4T1/SRs3-11, pGEX4T1/SRs21-30, pGEX4T1/SRs3137, pGEX4T1/SRs38-47 and pGEX4T1/SRs48-54 coding, respectively, for spectrin repeats 3–11, 21–30, 31–37, 38–47 and 48–54 of human Nesprin-2 fused to GST were generated by PCR-amplifying the respective sequences from cDNA derived from human BE cells and inserting them into the pGEX4T1 vector (GE Healthcare) as XhoINotI fragments. .. Plasmids GFP:PDZdom, GFP:PDZ(RH), GFP:PDZ(DH/PH) and GFP:PDZ(C-term) coding, respectively, for amino acid sequences 1–219, 220–701, 702–1152 or 1168–1522 of human PDZ RhoGEF fused to GFP were generated by PCRamplifying the respective sequences from mCitrine-YFP-ARHGEF11 plasmid and inserting them into the pEGFP-C1 vector (Clontech) as EcoRI-XhoI fragments. .. Plasmid pGEX4T1/SRs12-20 coding for spectrin repeats 12–20 of human Nesprin-2 fused to GST was generated by amplifying the respective sequence by PCR from cDNA derived from human BE cells and inserting it into the pGEX4T1 vector (GE Healthcare) as a SalI-NotI fragment.

    Article Title: Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1
    Article Snippet: Reagents were obtained from the following sources: DSP (Dithiobis(succinimidyl propionate)), TCI America (TCD2473); MLN4924, Cayman (15217); MG-132, Selleckchem (S2619); GFP-Trap magnetic agarose, ChromoTek (gtma-20); Protein G Sepharose, BioVision (6511); Ni-NTA agarose, QIAGEN (133203974); Anti-HA magnetic beads, Thermo Scientific (88836); Anti-FLAG magnetic beads, made in-house from NHS magnetic beads, Nacalai USA (TAS8848N1141-10MG) and Anti DYKDDDDK tag, Fujifilm (012-22383); Lipofectamine 2000, Invitrogen (11668019); RNase A, Research Products International (R21750); Puromycin dihydrochloride, Sigma-Aldrich (P8833); Blasticidin S hydrochloride, 10 mg/ml in HEPES buffer, Alfa Aesar (J67216); cOmplete Protease Inhibitor Cocktail, Roche (5056489001); ProLong Diamond Antifade Mountant with DAPI, Thermo Fisher (P36971); Clarity Western ECL Substrate, Bio-Rad (1705061). .. The SHKBP1 cDNA (Gene ID: 92799, a gift from Haiyuan Yu, Cornell University) was cloned into the pEGFP-C1 vector (Clontech) using EcoRI and KpnI to generate EGFP-SHKBP1, and into the p3xFLAG-CMV-10 vector (Sigma-Aldrich) using HindIII and KpnI to generate FLAG-SHKBP1. ..

    Article Title: Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis
    Article Snippet: Plasmids pGEX4T1/SRs3-11, pGEX4T1/SRs21-30, pGEX4T1/SRs31-37, pGEX4T1/SRs38-47 and pGEX4T1/SRs48-54 coding, respectively, for spectrin repeats 3–11, 21–30, 31–37, 38–47 and 48–54 of human Nesprin-2 fused to GST were generated by PCR-amplifying the respective sequences from cDNA derived from human BE cells and inserting them into the pGEX4T1 vector (GE Healthcare) as XhoI-NotI fragments. .. Plasmids GFP:PDZ dom , GFP:PDZ(RH), GFP:PDZ(DH/PH) and GFP:PDZ(C-term) coding, respectively, for amino acid sequences 1–219, 220–701, 702–1152 or 1168–1522 of human PDZ RhoGEF fused to GFP were generated by PCR-amplifying the respective sequences from mCitrine-YFP-ARHGEF11 plasmid and inserting them into the pEGFP-C1 vector (Clontech) as EcoRI-XhoI fragments. .. Plasmid pGEX4T1/SRs12-20 coding for spectrin repeats 12–20 of human Nesprin-2 fused to GST was generated by amplifying the respective sequence by PCR from cDNA derived from human BE cells and inserting it into the pGEX4T1 vector (GE Healthcare) as a SalI-NotI fragment.

    Article Title: Selective induction by statins of FAM134B-mediated sarcoplasmic reticulum (SR)-phagy degrades the SR calcium pump SERCA1 and contributes to myopathy
    Article Snippet: The coding sequence of mouse SERCA1 was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the NotI/XbaI site to generate pFLAG-SERCA1. .. To generate EGFP-SERCA1 and pmCherry-EGFP-SERCA1 expression plasmids, coding region of mouse SERCA1 was first cloned into the pEGFP-C1 vector (Clonetech) at the XhoI/SacII sites, and then EGFP-SERCA1 was subcloned into pmCherry-C1 vector (Clonetech) at SacII/XmaI sites. .. The coding sequence of mouse FAM134B-S cDNA was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the HindIII/EcoRI site to generate pFLAG-FAM134B-S, or cloned into pmCherry-C1 vector at the HindIII/EcoRI site to generate pmCherry-FAM134B-S.

    Article Title: Spuriously transcribed RNAs from CRISPR-sgRNA expression plasmids scaffold biomolecular condensate formation and hamper accurate genomic imaging
    Article Snippet: To generate the Streptococcus pyogenes dCas9 expression plasmid pdCas9, the coding region of dCas9 was first PCR amplified from pSLQ1658-dCas9-EGFP, a gift from Dr. Bo Huang and Dr. Stanley Qi (Addgene plasmid #51023) [ ], using forward primer 5′- ACTGCTGCTAGCGCTACCGGTCGCCACCATGGTGCCCAAAAAGAAGAGG-3′ and reverse primer 5′-ACCTGCGAATTCTTAGAACAGCTCCTCGCCC-3′. .. The PCR product was then inserted into the pEGFP-C1 vector (Clontech) digested with NheI and EcoRI to excise out EGFP. .. The MS2_EGFP and PP7_mCherry plasmids that encode MCP-EGFP and PCP-mCherry, respectively, were gifts form Dr. Daniel Larson (Addgene plasmids #61764 and #61763) [ ].

    Construct:

    Article Title: Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1
    Article Snippet: .. Resistant EGFP-SHKBP1 or 2xUBA-3xFLAG-SHKBP1 (2US) or GFP-SHKBP1 (F44A) were subcloned into the pCDH-CMV-MCS vector to yield the lentiviral plasmid. p62-related constructs were amplified from HA-p62, Addgene (28027), which was subcloned into pEGFP-C1 vector (Clontech) using EcoRI and KpnI to generate GFP-p62. ..

    Amplification:

    Article Title: Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1
    Article Snippet: .. Resistant EGFP-SHKBP1 or 2xUBA-3xFLAG-SHKBP1 (2US) or GFP-SHKBP1 (F44A) were subcloned into the pCDH-CMV-MCS vector to yield the lentiviral plasmid. p62-related constructs were amplified from HA-p62, Addgene (28027), which was subcloned into pEGFP-C1 vector (Clontech) using EcoRI and KpnI to generate GFP-p62. ..

    Article Title: Expression Analysis of Heavy-Chain-Only Antibodies in Cloudy Catshark and Japanese Bullhead Shark
    Article Snippet: .. The amplified PCR fragments were digested with EcoRI (Cat. No.: 1040A, Takara Bio Inc., Kusatsu, Shiga, Japan) and XhoI (Cat. No.: 1094A, Takara Bio Inc.) and then cloned into the pEGFP-C1 vector (Cat. No.: 632470, Takara Bio Inc.). ..

    Polymerase Chain Reaction:

    Article Title: UCHL1-Mediated Spastin Degradation Regulates Microtubule Severing and Hippocampal Neurite Outgrowth.
    Article Snippet: As a key component of the cytoskeleton, microtubule dynamic provides structural support for neurite outgrowth.. Spastin, a microtubule severing enzyme associated with hereditary spastic paraplegia (HSP), is crucial for the growth and branching of neuronal processes.. Thus, the activity and function of spastin need to be strictly regulated.

    Article Title: Expression Analysis of Heavy-Chain-Only Antibodies in Cloudy Catshark and Japanese Bullhead Shark
    Article Snippet: .. The amplified PCR fragments were digested with EcoRI (Cat. No.: 1040A, Takara Bio Inc., Kusatsu, Shiga, Japan) and XhoI (Cat. No.: 1094A, Takara Bio Inc.) and then cloned into the pEGFP-C1 vector (Cat. No.: 632470, Takara Bio Inc.). ..

    Article Title: Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis
    Article Snippet: Plasmids pGEX4T1/SRs3-11, pGEX4T1/SRs21-30, pGEX4T1/SRs31-37, pGEX4T1/SRs38-47 and pGEX4T1/SRs48-54 coding, respectively, for spectrin repeats 3–11, 21–30, 31–37, 38–47 and 48–54 of human Nesprin-2 fused to GST were generated by PCR-amplifying the respective sequences from cDNA derived from human BE cells and inserting them into the pGEX4T1 vector (GE Healthcare) as XhoI-NotI fragments. .. Plasmids GFP:PDZ dom , GFP:PDZ(RH), GFP:PDZ(DH/PH) and GFP:PDZ(C-term) coding, respectively, for amino acid sequences 1–219, 220–701, 702–1152 or 1168–1522 of human PDZ RhoGEF fused to GFP were generated by PCR-amplifying the respective sequences from mCitrine-YFP-ARHGEF11 plasmid and inserting them into the pEGFP-C1 vector (Clontech) as EcoRI-XhoI fragments. .. Plasmid pGEX4T1/SRs12-20 coding for spectrin repeats 12–20 of human Nesprin-2 fused to GST was generated by amplifying the respective sequence by PCR from cDNA derived from human BE cells and inserting it into the pGEX4T1 vector (GE Healthcare) as a SalI-NotI fragment.

    Article Title: Spuriously transcribed RNAs from CRISPR-sgRNA expression plasmids scaffold biomolecular condensate formation and hamper accurate genomic imaging
    Article Snippet: To generate the Streptococcus pyogenes dCas9 expression plasmid pdCas9, the coding region of dCas9 was first PCR amplified from pSLQ1658-dCas9-EGFP, a gift from Dr. Bo Huang and Dr. Stanley Qi (Addgene plasmid #51023) [ ], using forward primer 5′- ACTGCTGCTAGCGCTACCGGTCGCCACCATGGTGCCCAAAAAGAAGAGG-3′ and reverse primer 5′-ACCTGCGAATTCTTAGAACAGCTCCTCGCCC-3′. .. The PCR product was then inserted into the pEGFP-C1 vector (Clontech) digested with NheI and EcoRI to excise out EGFP. .. The MS2_EGFP and PP7_mCherry plasmids that encode MCP-EGFP and PCP-mCherry, respectively, were gifts form Dr. Daniel Larson (Addgene plasmids #61764 and #61763) [ ].

    Clone Assay:

    Article Title: UCHL1-Mediated Spastin Degradation Regulates Microtubule Severing and Hippocampal Neurite Outgrowth.
    Article Snippet: As a key component of the cytoskeleton, microtubule dynamic provides structural support for neurite outgrowth.. Spastin, a microtubule severing enzyme associated with hereditary spastic paraplegia (HSP), is crucial for the growth and branching of neuronal processes.. Thus, the activity and function of spastin need to be strictly regulated.

    Article Title: Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1
    Article Snippet: Reagents were obtained from the following sources: DSP (Dithiobis(succinimidyl propionate)), TCI America (TCD2473); MLN4924, Cayman (15217); MG-132, Selleckchem (S2619); GFP-Trap magnetic agarose, ChromoTek (gtma-20); Protein G Sepharose, BioVision (6511); Ni-NTA agarose, QIAGEN (133203974); Anti-HA magnetic beads, Thermo Scientific (88836); Anti-FLAG magnetic beads, made in-house from NHS magnetic beads, Nacalai USA (TAS8848N1141-10MG) and Anti DYKDDDDK tag, Fujifilm (012-22383); Lipofectamine 2000, Invitrogen (11668019); RNase A, Research Products International (R21750); Puromycin dihydrochloride, Sigma-Aldrich (P8833); Blasticidin S hydrochloride, 10 mg/ml in HEPES buffer, Alfa Aesar (J67216); cOmplete Protease Inhibitor Cocktail, Roche (5056489001); ProLong Diamond Antifade Mountant with DAPI, Thermo Fisher (P36971); Clarity Western ECL Substrate, Bio-Rad (1705061). .. The SHKBP1 cDNA (Gene ID: 92799, a gift from Haiyuan Yu, Cornell University) was cloned into the pEGFP-C1 vector (Clontech) using EcoRI and KpnI to generate EGFP-SHKBP1, and into the p3xFLAG-CMV-10 vector (Sigma-Aldrich) using HindIII and KpnI to generate FLAG-SHKBP1. ..

    Article Title: Expression Analysis of Heavy-Chain-Only Antibodies in Cloudy Catshark and Japanese Bullhead Shark
    Article Snippet: .. The amplified PCR fragments were digested with EcoRI (Cat. No.: 1040A, Takara Bio Inc., Kusatsu, Shiga, Japan) and XhoI (Cat. No.: 1094A, Takara Bio Inc.) and then cloned into the pEGFP-C1 vector (Cat. No.: 632470, Takara Bio Inc.). ..

    Article Title: Selective induction by statins of FAM134B-mediated sarcoplasmic reticulum (SR)-phagy degrades the SR calcium pump SERCA1 and contributes to myopathy
    Article Snippet: The coding sequence of mouse SERCA1 was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the NotI/XbaI site to generate pFLAG-SERCA1. .. To generate EGFP-SERCA1 and pmCherry-EGFP-SERCA1 expression plasmids, coding region of mouse SERCA1 was first cloned into the pEGFP-C1 vector (Clonetech) at the XhoI/SacII sites, and then EGFP-SERCA1 was subcloned into pmCherry-C1 vector (Clonetech) at SacII/XmaI sites. .. The coding sequence of mouse FAM134B-S cDNA was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the HindIII/EcoRI site to generate pFLAG-FAM134B-S, or cloned into pmCherry-C1 vector at the HindIII/EcoRI site to generate pmCherry-FAM134B-S.

    Generated:

    Article Title: Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis.
    Article Snippet: Plasmids pGEX4T1/SRs3-11, pGEX4T1/SRs21-30, pGEX4T1/SRs3137, pGEX4T1/SRs38-47 and pGEX4T1/SRs48-54 coding, respectively, for spectrin repeats 3–11, 21–30, 31–37, 38–47 and 48–54 of human Nesprin-2 fused to GST were generated by PCR-amplifying the respective sequences from cDNA derived from human BE cells and inserting them into the pGEX4T1 vector (GE Healthcare) as XhoINotI fragments. .. Plasmids GFP:PDZdom, GFP:PDZ(RH), GFP:PDZ(DH/PH) and GFP:PDZ(C-term) coding, respectively, for amino acid sequences 1–219, 220–701, 702–1152 or 1168–1522 of human PDZ RhoGEF fused to GFP were generated by PCRamplifying the respective sequences from mCitrine-YFP-ARHGEF11 plasmid and inserting them into the pEGFP-C1 vector (Clontech) as EcoRI-XhoI fragments. .. Plasmid pGEX4T1/SRs12-20 coding for spectrin repeats 12–20 of human Nesprin-2 fused to GST was generated by amplifying the respective sequence by PCR from cDNA derived from human BE cells and inserting it into the pGEX4T1 vector (GE Healthcare) as a SalI-NotI fragment.

    Article Title: Tension-sensitive LINC-RhoA signaling prevents chromatin bridge breakage in cytokinesis
    Article Snippet: Plasmids pGEX4T1/SRs3-11, pGEX4T1/SRs21-30, pGEX4T1/SRs31-37, pGEX4T1/SRs38-47 and pGEX4T1/SRs48-54 coding, respectively, for spectrin repeats 3–11, 21–30, 31–37, 38–47 and 48–54 of human Nesprin-2 fused to GST were generated by PCR-amplifying the respective sequences from cDNA derived from human BE cells and inserting them into the pGEX4T1 vector (GE Healthcare) as XhoI-NotI fragments. .. Plasmids GFP:PDZ dom , GFP:PDZ(RH), GFP:PDZ(DH/PH) and GFP:PDZ(C-term) coding, respectively, for amino acid sequences 1–219, 220–701, 702–1152 or 1168–1522 of human PDZ RhoGEF fused to GFP were generated by PCR-amplifying the respective sequences from mCitrine-YFP-ARHGEF11 plasmid and inserting them into the pEGFP-C1 vector (Clontech) as EcoRI-XhoI fragments. .. Plasmid pGEX4T1/SRs12-20 coding for spectrin repeats 12–20 of human Nesprin-2 fused to GST was generated by amplifying the respective sequence by PCR from cDNA derived from human BE cells and inserting it into the pGEX4T1 vector (GE Healthcare) as a SalI-NotI fragment.

    Expressing:

    Article Title: Selective induction by statins of FAM134B-mediated sarcoplasmic reticulum (SR)-phagy degrades the SR calcium pump SERCA1 and contributes to myopathy
    Article Snippet: The coding sequence of mouse SERCA1 was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the NotI/XbaI site to generate pFLAG-SERCA1. .. To generate EGFP-SERCA1 and pmCherry-EGFP-SERCA1 expression plasmids, coding region of mouse SERCA1 was first cloned into the pEGFP-C1 vector (Clonetech) at the XhoI/SacII sites, and then EGFP-SERCA1 was subcloned into pmCherry-C1 vector (Clonetech) at SacII/XmaI sites. .. The coding sequence of mouse FAM134B-S cDNA was cloned into p3XFlag-CMV-7.1 vector (Sigma) at the HindIII/EcoRI site to generate pFLAG-FAM134B-S, or cloned into pmCherry-C1 vector at the HindIII/EcoRI site to generate pmCherry-FAM134B-S.



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