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alicator ligation independent cloning (lic) and expression kit  (Thermo Fisher)


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    Thermo Fisher alicator ligation independent cloning (lic) and expression kit
    Alicator Ligation Independent Cloning (Lic) And Expression Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alicator+ligation+independent+cloning+and+expression+system/alicator+ligation+independent+cloning+and+expression+system/pm40181138-38-7-9
    Average 90 stars, based on 1 article reviews
    alicator ligation independent cloning (lic) and expression kit - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Polymerase Chain Reaction:

    Article Title: Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment.
    Article Snippet: .. Obtained PCR products were cloned into pLate52 and pLate31 vectors, respectively for the NH-his-tagged and CH-his-tagged variants, using an aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, MA, USA). ..

    Article Title: Enzymatic Synthesis of a Polyketide/Nonribosomal Peptide Hybrid Antibiotic, Salivabactin.
    Article Snippet: Salivabactin is a newly identified polyketide/nonribosomal peptide (PK/NRP) from a human oral probiotic, possessing a unique chemical structure and outstanding antibiotic activities.. Although the biosynthetic gene cluster for salivabactin is known, the enzymatic logic that governs the synthesis of salivabactin has not yet been fully studied.. In this work, we dissected the biosynthetic pathway for salivabactin using biochemical analysis.

    Clone Assay:

    Article Title: Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment.
    Article Snippet: .. Obtained PCR products were cloned into pLate52 and pLate31 vectors, respectively for the NH-his-tagged and CH-his-tagged variants, using an aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, MA, USA). ..

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Article Title: Genome Sequencing and Assembly of Enterotoxigenic Escherichia coli E9034A: Role of LngA, CstH, and FliC in Intestinal Cell Colonization and the Release of the Proinflammatory Cytokine IL-8
    Article Snippet: .. The lngA , cstH , and fliC genes were cloned and inserted into the pLATE31 plasmid according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, Santa Clara, CA, USA). ..

    Ligation:

    Article Title: Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment.
    Article Snippet: .. Obtained PCR products were cloned into pLate52 and pLate31 vectors, respectively for the NH-his-tagged and CH-his-tagged variants, using an aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, MA, USA). ..

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Article Title: Enzymatic Synthesis of a Polyketide/Nonribosomal Peptide Hybrid Antibiotic, Salivabactin.
    Article Snippet: Salivabactin is a newly identified polyketide/nonribosomal peptide (PK/NRP) from a human oral probiotic, possessing a unique chemical structure and outstanding antibiotic activities.. Although the biosynthetic gene cluster for salivabactin is known, the enzymatic logic that governs the synthesis of salivabactin has not yet been fully studied.. In this work, we dissected the biosynthetic pathway for salivabactin using biochemical analysis.

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Article Title: The incC Sequence Is Required for R27 Plasmid Stability
    Article Snippet: .. The recombinant plasmid for C-terminal His-tagged R27-encoded E protein overexpression was obtained following the instructions of ALICator Ligation Independent Cloning and Expression System (Thermo Scientific) using primers RepECtermFor and RepECtermRev ( Supplementary Table ). ..

    Article Title: Characterization of Enzymatic Activity of MlrB and MlrC Proteins Involved in Bacterial Degradation of Cyanotoxins Microcystins
    Article Snippet: .. After amplification with mlrBF and mlrBR primers , mlrB was inserted into pLATE31 vector using an aLICator Ligation Independent Cloning and Expression System (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instruction. ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Article Title: Genome Sequencing and Assembly of Enterotoxigenic Escherichia coli E9034A: Role of LngA, CstH, and FliC in Intestinal Cell Colonization and the Release of the Proinflammatory Cytokine IL-8
    Article Snippet: .. The lngA , cstH , and fliC genes were cloned and inserted into the pLATE31 plasmid according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, Santa Clara, CA, USA). ..

    Cloning:

    Article Title: Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment.
    Article Snippet: .. Obtained PCR products were cloned into pLate52 and pLate31 vectors, respectively for the NH-his-tagged and CH-his-tagged variants, using an aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, MA, USA). ..

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Article Title: Enzymatic Synthesis of a Polyketide/Nonribosomal Peptide Hybrid Antibiotic, Salivabactin.
    Article Snippet: Salivabactin is a newly identified polyketide/nonribosomal peptide (PK/NRP) from a human oral probiotic, possessing a unique chemical structure and outstanding antibiotic activities.. Although the biosynthetic gene cluster for salivabactin is known, the enzymatic logic that governs the synthesis of salivabactin has not yet been fully studied.. In this work, we dissected the biosynthetic pathway for salivabactin using biochemical analysis.

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Article Title: The incC Sequence Is Required for R27 Plasmid Stability
    Article Snippet: .. The recombinant plasmid for C-terminal His-tagged R27-encoded E protein overexpression was obtained following the instructions of ALICator Ligation Independent Cloning and Expression System (Thermo Scientific) using primers RepECtermFor and RepECtermRev ( Supplementary Table ). ..

    Article Title: Characterization of Enzymatic Activity of MlrB and MlrC Proteins Involved in Bacterial Degradation of Cyanotoxins Microcystins
    Article Snippet: .. After amplification with mlrBF and mlrBR primers , mlrB was inserted into pLATE31 vector using an aLICator Ligation Independent Cloning and Expression System (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instruction. ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Article Title: Genome Sequencing and Assembly of Enterotoxigenic Escherichia coli E9034A: Role of LngA, CstH, and FliC in Intestinal Cell Colonization and the Release of the Proinflammatory Cytokine IL-8
    Article Snippet: .. The lngA , cstH , and fliC genes were cloned and inserted into the pLATE31 plasmid according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, Santa Clara, CA, USA). ..

    Binding Assay:

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Amplification:

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Article Title: Characterization of Enzymatic Activity of MlrB and MlrC Proteins Involved in Bacterial Degradation of Cyanotoxins Microcystins
    Article Snippet: .. After amplification with mlrBF and mlrBR primers , mlrB was inserted into pLATE31 vector using an aLICator Ligation Independent Cloning and Expression System (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instruction. ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Derivative Assay:

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Isolation:

    Article Title: Utility of in silico-identified-peptides in spike-S1 domain and nucleocapsid of SARS-CoV-2 for antibody detection in COVID-19 patients and antibody production.
    Article Snippet: .. The SARS-CoV-2 receptor binding domain (RBD) was amplified from a template of cDNA derived from a clinical isolation of SARS-CoV-2 and cloned into pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Cat# K1261 Thermo Scientific). .. The cDNA of SARS-CoV-2 protein N was also obtained from clinical isolation and cloned into pLATE-51 (Cat# K1251 Thermo Scientific). pLATE-RBD with C-terminal hexahistadine (or 6xHIS) tags and pLATE-51-N with six N-terminal histidine tags were used for the transformation of the Rosetta strain of E. coli, and IMAC purification was performed under native conditions.

    Plasmid Preparation:

    Article Title: Enzymatic Synthesis of a Polyketide/Nonribosomal Peptide Hybrid Antibiotic, Salivabactin.
    Article Snippet: Salivabactin is a newly identified polyketide/nonribosomal peptide (PK/NRP) from a human oral probiotic, possessing a unique chemical structure and outstanding antibiotic activities.. Although the biosynthetic gene cluster for salivabactin is known, the enzymatic logic that governs the synthesis of salivabactin has not yet been fully studied.. In this work, we dissected the biosynthetic pathway for salivabactin using biochemical analysis.

    Article Title: The incC Sequence Is Required for R27 Plasmid Stability
    Article Snippet: .. The recombinant plasmid for C-terminal His-tagged R27-encoded E protein overexpression was obtained following the instructions of ALICator Ligation Independent Cloning and Expression System (Thermo Scientific) using primers RepECtermFor and RepECtermRev ( Supplementary Table ). ..

    Article Title: Characterization of Enzymatic Activity of MlrB and MlrC Proteins Involved in Bacterial Degradation of Cyanotoxins Microcystins
    Article Snippet: .. After amplification with mlrBF and mlrBR primers , mlrB was inserted into pLATE31 vector using an aLICator Ligation Independent Cloning and Expression System (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instruction. ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Article Title: Genome Sequencing and Assembly of Enterotoxigenic Escherichia coli E9034A: Role of LngA, CstH, and FliC in Intestinal Cell Colonization and the Release of the Proinflammatory Cytokine IL-8
    Article Snippet: .. The lngA , cstH , and fliC genes were cloned and inserted into the pLATE31 plasmid according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, Santa Clara, CA, USA). ..

    Transformation Assay:

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Purification:

    Article Title: Clinical features and severe acute respiratory syndrome-coronavirus-2 structural protein-based serology of Mexican children and adolescents with coronavirus disease 2019
    Article Snippet: .. The SARS-CoV-2 receptor-binding domain (RBD) was amplified from the cDNA of a SARS-CoV-2 clinical isolate and cloned in pLATE-31 according to the protocol of the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific). pLATE-RBD with a C-terminal six histidine tag was transformed into Escherichia coli strain Rosetta and purified using IMAC in native conditions. ..

    Recombinant:

    Article Title: The incC Sequence Is Required for R27 Plasmid Stability
    Article Snippet: .. The recombinant plasmid for C-terminal His-tagged R27-encoded E protein overexpression was obtained following the instructions of ALICator Ligation Independent Cloning and Expression System (Thermo Scientific) using primers RepECtermFor and RepECtermRev ( Supplementary Table ). ..

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..

    Over Expression:

    Article Title: The incC Sequence Is Required for R27 Plasmid Stability
    Article Snippet: .. The recombinant plasmid for C-terminal His-tagged R27-encoded E protein overexpression was obtained following the instructions of ALICator Ligation Independent Cloning and Expression System (Thermo Scientific) using primers RepECtermFor and RepECtermRev ( Supplementary Table ). ..

    Expressing:

    Article Title: Effects of lng Mutations on LngA Expression, Processing, and CS21 Assembly in Enterotoxigenic Escherichia coli E9034A
    Article Snippet: Restriction enzymes were purchased from Promega (Promega Corporation, WI, USA) and were used according to the manufacturer's recommendations. .. Primer design, amplification, cloning and expression of lngB and lng genes in the pLATE31 plasmid were conducted according to the aLICator Ligation Independent Cloning and Expression System (Thermo Scientific, CA, USA). pLATE31 and the recombinant expression plasmid pLATE31-lngB and pLATE31-lngC were transformed into E. coli BL21 (DE3). ..



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