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bsmbidigested plenticrispr v2 vector backbone  (Addgene inc)


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    Structured Review

    Addgene inc bsmbidigested plenticrispr v2 vector backbone
    Bsmbidigested Plenticrispr V2 Vector Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 6234 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/backbone+vector/lentiCRISPR+v2+(Plasmid+%2352961)/pm42880285-1487-34-38
    Average 96 stars, based on 6234 article reviews
    bsmbidigested plenticrispr v2 vector backbone - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Expressing:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Plasmid Preparation:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Article Title: The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis.
    Article Snippet: The LYN-EGFP overexpression plasmid (mEGFP-N1-LYN) and ACAT1-EGFP overexpression plasmid (mEGFP-N1-ACAT1) were constructed by cloning the corresponding coding sequences into the mEGFP-N1 vector from Addgene (#54767); the ACAT1mCherry overexpression plasmid (pmCherry-C1-ACAT1) were constructed by cloning the corresponding coding sequences into the pmCherry-C1 vector; the LYN Y397D-EGFP overexpression plasmid (mEGFP-N1-LYN Y397D), ACAT1 Y214D, Y219D, Y407D-EGFP overexpression plasmid (mEGFP-N1-ACAT1-M), and ACAT1 Y214D, Y219D, Y407D-EGFP overexpression plasmid (pmCherry-C1-ACAT1-M) were constructed using the Fast SiteDirected Mutagenesis Kit (Tiangen, KM101). .. For gene knockout, Cas-Designer (http://www.rgenome.net/casdesigner/) was used to design the sgRNAs (sgRNA1: TCTATTCCAACAGGAAATAT; sgRNA2: CCAGTAAGTAGACTAGTCTC; sgRNA3: GTGGCCTTATACCCTTATGA; sgRNA4: GCTGGG ACCTACTTGCTGCT); sgRNAs were inserted into the backbone vector from Addgene (#51133). ..

    Article Title: CRISPR-based screening identifies the role of KRAB-containing transcription factors ZIM3 and ZNF394 in human major zygotic genome activation.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Bowtie2 v2.5.4 Langmead et al.59 https://bowtie-bio.sourceforge.net/bowtie2/ index.shtml MAC2 v2.1.4 Zhang et al.60 https://github.com/jdavisturak/MACS2-2.1.1.20160309 Deeptools v3.3.0 Ramı́rez et al.61 https://test-argparse-readoc.readthedocs.io/ en/latest/content/installation.html CHIPseeker v1.30.3 Wang et al.62 https://bioconductor.org/packages/release/ bioc/html/ChIPseeker.html DiffBind v3.4.11 Cancer Research UK’s Cambridge Research Institute https://bioconductor.org/packages/release/ bioc/html/DiffBind.html MEME-suite v5.5.7 Timothy et al.63 https://meme-suite.org Graphpad Prism v9.0 Dotmatics https://www.graphpad.com/scientific-software/ prism/www.graphpad.com/scientific-software/ prism/ Other GTRD database Yevshin et al.49 http://gtrd.biouml.org DAVID database for GO and KEGG analysis Sherman et al.64 https://davidbioinformatics.nih.gov/ STRING database for PPI analysis Szklarczyk et al.65 N/A hORFeome Broad Institute N/A Cell Reports 44, 116015, August 26, 2025 23 .. For plasmid PB-idCas9-VPR-NeoR, the backbone vector was originated from PB-TRE-dCas9-VPR (addgene#63800), while the HygR sequence was replaced by NeoR sequence. .. For plasmid PB-DUXA-pMaxGFP-NLS-PGK-HygR, the regulatory sequence started from − 2 kb to transcription start site (TSS) of human DUXA gene was synthesized by Genscript.

    Article Title: The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis.
    Article Snippet: N2a and stable RhoBS73F/S73F cells were cultured in DMEM (Gibco, 11965092) containing 10% fetal bovine serum (FBS, Clark Bioscience). .. To construct the RhoBS73F/S73F mutant N2a cell line, sgRNA targeting the murine-derived locus was inserted into the backbone vector from Addgene (#51133). ..

    Article Title: LIPA , a risk locus for coronary artery disease: decoding the variant-to-function relationship
    Article Snippet: .. Specifically, mouse Lipa open reading frame ( NM_001111100 ) was cloned into the backbone vector (Addgene, 74285) 28 with a final construct (left homologous arm-CAG-loxP-STOP-loxP-Lipa-IRES-eGFP-right homologous arm) for the knock-in (KI) of the insert into the Rosa26 locus ( Lipa KI/WT ) and was bred to obtain ( Lipa KI/KI ). ..

    Article Title: A high affinity Sybody blocks Cofilin-1 binding to F-actin in vitro and in cancer cells.
    Article Snippet: .. For the construction of the pET AviTag-His6-Cofilin-1 vector (Plasmid 1), Cofilin1 cDNA was amplified using Primer 1 and Primer 2, while the backbone vector (pET Biotin His6 FlAsH LIC cloning vector, Addgene Plasmid #30184, Addgene, Massachusetts, USA) was amplified with Primer 3 and Primer 4. .. Similarly, for the pSF 10His-GFP-TEV-Cofilin-1 (Plasmid 2) vector, the Cofilin-1 cDNA was amplified from the pET AviTag-His6-Cofilin-1 vector (Plasmid 1) using Primer 5 and Primer 6, while the backbone (pSF 10His-GFP-TEV-ITPKA vector, Plasmid 11 see [36] was amplified using Primer 7 and Primer 8.

    Bioprocessing:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Modification:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Generated:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Sequencing:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Article Title: CRISPR-based screening identifies the role of KRAB-containing transcription factors ZIM3 and ZNF394 in human major zygotic genome activation.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Bowtie2 v2.5.4 Langmead et al.59 https://bowtie-bio.sourceforge.net/bowtie2/ index.shtml MAC2 v2.1.4 Zhang et al.60 https://github.com/jdavisturak/MACS2-2.1.1.20160309 Deeptools v3.3.0 Ramı́rez et al.61 https://test-argparse-readoc.readthedocs.io/ en/latest/content/installation.html CHIPseeker v1.30.3 Wang et al.62 https://bioconductor.org/packages/release/ bioc/html/ChIPseeker.html DiffBind v3.4.11 Cancer Research UK’s Cambridge Research Institute https://bioconductor.org/packages/release/ bioc/html/DiffBind.html MEME-suite v5.5.7 Timothy et al.63 https://meme-suite.org Graphpad Prism v9.0 Dotmatics https://www.graphpad.com/scientific-software/ prism/www.graphpad.com/scientific-software/ prism/ Other GTRD database Yevshin et al.49 http://gtrd.biouml.org DAVID database for GO and KEGG analysis Sherman et al.64 https://davidbioinformatics.nih.gov/ STRING database for PPI analysis Szklarczyk et al.65 N/A hORFeome Broad Institute N/A Cell Reports 44, 116015, August 26, 2025 23 .. For plasmid PB-idCas9-VPR-NeoR, the backbone vector was originated from PB-TRE-dCas9-VPR (addgene#63800), while the HygR sequence was replaced by NeoR sequence. .. For plasmid PB-DUXA-pMaxGFP-NLS-PGK-HygR, the regulatory sequence started from − 2 kb to transcription start site (TSS) of human DUXA gene was synthesized by Genscript.

    Polymerase Chain Reaction:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Amplification:

    Article Title: In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.
    Article Snippet: 1Department of Pharmacology, Yonsei University College ofMedicine, Seoul 03722, Republic of Korea; 2Brain Korea 21 Plus Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 3ConveRgence mEDIcine research cenTer (CREDIT), ASAN Institute for Life Sciences, ASAN Medical Center, Seoul 05505, Republic of Korea; 4Department of Cell and Genetic Engineering, ASAN Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea; 5JES Clinic, Incheon 21550, Republic of Korea; 6Department of PrecisionMedicine, SungkyunkwanUniversity School of Medicine, Suwon 16419, Republic of Korea; 7Center for Nanomedicine, Institute for Basic Science, Seoul 03722, Republic of Korea; 8Graduate Program of Nano Biomedical Engineering, Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea; 9Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 10Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; 11Woo Choo Lee Institute for Precision Drug

    Article Title: SWI/SNF ATPase silenced HLF potentiates lung metastasis in solid cancers.
    Article Snippet: Virus Infection For lentiviral plasmids, 293 T cells were used for virus production by co-transfection of the psPAX2 (Addgene, 12260) and pMD2.G (Addgene, 12259) in Opti-MEM with the addition of Lipofectamine 3000. .. The pFETCh_Donor (EMM0021, Addgene #63934) backbone vector was digested using BsaI and BbsI, followed by single step gibson assembly reaction with amplified gBlocks. ..

    Article Title: A high affinity Sybody blocks Cofilin-1 binding to F-actin in vitro and in cancer cells.
    Article Snippet: .. For the construction of the pET AviTag-His6-Cofilin-1 vector (Plasmid 1), Cofilin1 cDNA was amplified using Primer 1 and Primer 2, while the backbone vector (pET Biotin His6 FlAsH LIC cloning vector, Addgene Plasmid #30184, Addgene, Massachusetts, USA) was amplified with Primer 3 and Primer 4. .. Similarly, for the pSF 10His-GFP-TEV-Cofilin-1 (Plasmid 2) vector, the Cofilin-1 cDNA was amplified from the pET AviTag-His6-Cofilin-1 vector (Plasmid 1) using Primer 5 and Primer 6, while the backbone (pSF 10His-GFP-TEV-ITPKA vector, Plasmid 11 see [36] was amplified using Primer 7 and Primer 8.

    Gene Knockout:

    Article Title: The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis.
    Article Snippet: The LYN-EGFP overexpression plasmid (mEGFP-N1-LYN) and ACAT1-EGFP overexpression plasmid (mEGFP-N1-ACAT1) were constructed by cloning the corresponding coding sequences into the mEGFP-N1 vector from Addgene (#54767); the ACAT1mCherry overexpression plasmid (pmCherry-C1-ACAT1) were constructed by cloning the corresponding coding sequences into the pmCherry-C1 vector; the LYN Y397D-EGFP overexpression plasmid (mEGFP-N1-LYN Y397D), ACAT1 Y214D, Y219D, Y407D-EGFP overexpression plasmid (mEGFP-N1-ACAT1-M), and ACAT1 Y214D, Y219D, Y407D-EGFP overexpression plasmid (pmCherry-C1-ACAT1-M) were constructed using the Fast SiteDirected Mutagenesis Kit (Tiangen, KM101). .. For gene knockout, Cas-Designer (http://www.rgenome.net/casdesigner/) was used to design the sgRNAs (sgRNA1: TCTATTCCAACAGGAAATAT; sgRNA2: CCAGTAAGTAGACTAGTCTC; sgRNA3: GTGGCCTTATACCCTTATGA; sgRNA4: GCTGGG ACCTACTTGCTGCT); sgRNAs were inserted into the backbone vector from Addgene (#51133). ..

    Construct:

    Article Title: The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis.
    Article Snippet: N2a and stable RhoBS73F/S73F cells were cultured in DMEM (Gibco, 11965092) containing 10% fetal bovine serum (FBS, Clark Bioscience). .. To construct the RhoBS73F/S73F mutant N2a cell line, sgRNA targeting the murine-derived locus was inserted into the backbone vector from Addgene (#51133). ..

    Article Title: LIPA , a risk locus for coronary artery disease: decoding the variant-to-function relationship
    Article Snippet: .. Specifically, mouse Lipa open reading frame ( NM_001111100 ) was cloned into the backbone vector (Addgene, 74285) 28 with a final construct (left homologous arm-CAG-loxP-STOP-loxP-Lipa-IRES-eGFP-right homologous arm) for the knock-in (KI) of the insert into the Rosa26 locus ( Lipa KI/WT ) and was bred to obtain ( Lipa KI/KI ). ..

    Mutagenesis:

    Article Title: The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis.
    Article Snippet: N2a and stable RhoBS73F/S73F cells were cultured in DMEM (Gibco, 11965092) containing 10% fetal bovine serum (FBS, Clark Bioscience). .. To construct the RhoBS73F/S73F mutant N2a cell line, sgRNA targeting the murine-derived locus was inserted into the backbone vector from Addgene (#51133). ..

    Clone Assay:

    Article Title: LIPA , a risk locus for coronary artery disease: decoding the variant-to-function relationship
    Article Snippet: .. Specifically, mouse Lipa open reading frame ( NM_001111100 ) was cloned into the backbone vector (Addgene, 74285) 28 with a final construct (left homologous arm-CAG-loxP-STOP-loxP-Lipa-IRES-eGFP-right homologous arm) for the knock-in (KI) of the insert into the Rosa26 locus ( Lipa KI/WT ) and was bred to obtain ( Lipa KI/KI ). ..

    Knock-In:

    Article Title: LIPA , a risk locus for coronary artery disease: decoding the variant-to-function relationship
    Article Snippet: .. Specifically, mouse Lipa open reading frame ( NM_001111100 ) was cloned into the backbone vector (Addgene, 74285) 28 with a final construct (left homologous arm-CAG-loxP-STOP-loxP-Lipa-IRES-eGFP-right homologous arm) for the knock-in (KI) of the insert into the Rosa26 locus ( Lipa KI/WT ) and was bred to obtain ( Lipa KI/KI ). ..

    other:

    Article Title: SWI/SNF ATPase silenced HLF potentiates lung metastasis in solid cancers
    Article Snippet: For pLX304- FOSB / AJAP1 / HTRA1 , pDONR201- FOSB (HsCD00001737)/ pDONR221- AJAP1 (HsCD00877134)/ pDONR221- HTRA1 (HsCD00860462) were acquired from DNASU, and were cloned into pLX304 backbone (Addgene, 25890).

    Cloning:

    Article Title: A high affinity Sybody blocks Cofilin-1 binding to F-actin in vitro and in cancer cells.
    Article Snippet: .. For the construction of the pET AviTag-His6-Cofilin-1 vector (Plasmid 1), Cofilin1 cDNA was amplified using Primer 1 and Primer 2, while the backbone vector (pET Biotin His6 FlAsH LIC cloning vector, Addgene Plasmid #30184, Addgene, Massachusetts, USA) was amplified with Primer 3 and Primer 4. .. Similarly, for the pSF 10His-GFP-TEV-Cofilin-1 (Plasmid 2) vector, the Cofilin-1 cDNA was amplified from the pET AviTag-His6-Cofilin-1 vector (Plasmid 1) using Primer 5 and Primer 6, while the backbone (pSF 10His-GFP-TEV-ITPKA vector, Plasmid 11 see [36] was amplified using Primer 7 and Primer 8.



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