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expression vector plpcx  (TaKaRa)


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    TaKaRa expression vector plpcx
    Expression Vector Plpcx, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 26 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plpcx+expression+vector/LRCX+Retroviral+Vector+Set/pm40890526-204-7-10
    Average 95 stars, based on 26 article reviews
    expression vector plpcx - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Construct:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Sequencing:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression.
    Article Snippet: After reverse transcription with hexamers (Expand RT; Roche), ZNRD1 was amplified using the following primers, which introduced, respectively, EcoRI and ClaI (shown in boldface type): 5′-GAATTCgccaccATGTCTGTCATGGACCTCGCCAATAC-3′ and 5′-ATCGATggctcaAGAGTCTTCCTTCTCCTGGAACTTG-3′. .. PCR products were digested with EcoRI and ClaI, introduced into the pLPCX expression vector (Clontech), and checked by sequencing. ..

    Generated:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366).35 Deletion mutants were generated using the Phusion Site- Directed Mutagenesis Kit (Thermo Fisher Scientific). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. Generation and Expression of Membrane-bound PLA2R1 Deletion Mutants We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366). .. 35 Deletion mutants were generated using the Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific).

    Polymerase Chain Reaction:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366).35 Deletion mutants were generated using the Phusion Site- Directed Mutagenesis Kit (Thermo Fisher Scientific). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. Generation and Expression of Membrane-bound PLA2R1 Deletion Mutants We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366). .. 35 Deletion mutants were generated using the Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific).

    Article Title: ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression.
    Article Snippet: After reverse transcription with hexamers (Expand RT; Roche), ZNRD1 was amplified using the following primers, which introduced, respectively, EcoRI and ClaI (shown in boldface type): 5′-GAATTCgccaccATGTCTGTCATGGACCTCGCCAATAC-3′ and 5′-ATCGATggctcaAGAGTCTTCCTTCTCCTGGAACTTG-3′. .. PCR products were digested with EcoRI and ClaI, introduced into the pLPCX expression vector (Clontech), and checked by sequencing. ..

    Clone Assay:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366).35 Deletion mutants were generated using the Phusion Site- Directed Mutagenesis Kit (Thermo Fisher Scientific). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. Generation and Expression of Membrane-bound PLA2R1 Deletion Mutants We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366). .. 35 Deletion mutants were generated using the Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific).

    Expressing:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366).35 Deletion mutants were generated using the Phusion Site- Directed Mutagenesis Kit (Thermo Fisher Scientific). ..

    Article Title: A proximity ligation assay using transiently transfected, epitope-tagged proteins: application for in situ detection of dimerized receptor tyrosine kinases.
    Article Snippet: Methods and materials Expression constructs Human wild-type EGFR-encoding cDNA (lacking stop codon) was PCR-amplified from the pGEM7zf(-):EGFRwt (Promega, Madison, WI, USA) shuttle vector (primer sequences available in Supplementary Table S1) and cloned into pCR2.1-TOPO using the TOPO-TA system (Invitrogen, Burlington, ON, Canada) for sequence verification. .. EGFRwt-pCR2.1-TOPO was SacII-digested and blunt-end–cloned into the HindIII site of pLPCX expression vector (Clontech, Mountain View, CA, USA) to ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. Generation and Expression of Membrane-bound PLA2R1 Deletion Mutants We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366). .. 35 Deletion mutants were generated using the Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific).

    Article Title: ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression.
    Article Snippet: After reverse transcription with hexamers (Expand RT; Roche), ZNRD1 was amplified using the following primers, which introduced, respectively, EcoRI and ClaI (shown in boldface type): 5′-GAATTCgccaccATGTCTGTCATGGACCTCGCCAATAC-3′ and 5′-ATCGATggctcaAGAGTCTTCCTTCTCCTGGAACTTG-3′. .. PCR products were digested with EcoRI and ClaI, introduced into the pLPCX expression vector (Clontech), and checked by sequencing. ..

    Plasmid Preparation:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: PLA2R1 deletion constructs were designed as previously described.11 As a first step, the wild-type human PLA2R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA2R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Article Title: ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression.
    Article Snippet: After reverse transcription with hexamers (Expand RT; Roche), ZNRD1 was amplified using the following primers, which introduced, respectively, EcoRI and ClaI (shown in boldface type): 5′-GAATTCgccaccATGTCTGTCATGGACCTCGCCAATAC-3′ and 5′-ATCGATggctcaAGAGTCTTCCTTCTCCTGGAACTTG-3′. .. PCR products were digested with EcoRI and ClaI, introduced into the pLPCX expression vector (Clontech), and checked by sequencing. ..

    Mutagenesis:

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366).35 Deletion mutants were generated using the Phusion Site- Directed Mutagenesis Kit (Thermo Fisher Scientific). ..

    Proximity Ligation Assay:

    Article Title: Clinical Relevance of Domain-Specific Phospholipase A 2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy
    Article Snippet: 11 As a first step, the wild-type human PLA 2 R1 cDNA (GenBank NM007366) was cloned into the pGEM-Teasy vector (Promega, Madison, WI). .. The PLA 2 R1 deletion constructs, to which an HA-tag was fused to the C terminus of the coding sequence, were then generated by PCR and cloned into the pLPCX expression vector (#631511; Clontech Laboratories Inc.). ..

    Membrane:

    Article Title: Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy
    Article Snippet: .. Generation and Expression of Membrane-bound PLA2R1 Deletion Mutants We generated the series of human PLA2R1 deletion mutants by PCR and cloned them into the pLPCX expression vector (Clontech), as previously described for wild-type human PLA2R1 (GenBank NM 007366). .. 35 Deletion mutants were generated using the Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific).



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