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bglii sali site  (TaKaRa)


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    Structured Review

    TaKaRa bglii sali site
    Bglii Sali Site, supplied by TaKaRa, used in various techniques. Bioz Stars score: 97/100, based on 3916 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bglii+site/Bgl+II/pm41928225-78-6-12
    Average 97 stars, based on 3916 article reviews
    bglii sali site - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Expressing:

    Article Title: Development of a novel system for the expression and production of recombinant monoclonal antibody, tocilizumab, using Pichia pastoris.
    Article Snippet: The development of anti-interleukin-6-receptor (IL6R) recombinant monoclonal antibody Tocilizumab (TCZ) production in a methylotrophic yeast Pichia pastoris was the focus of this research work.. The molecular weight of full-length TCZ is approximately 148 kDa.. A bicistronic expression vector with both heavy and light chain genes was constructed within individual inducible alcohol oxidase promoters and secretory signal peptides.

    Sequencing:

    Article Title: Development of a novel system for the expression and production of recombinant monoclonal antibody, tocilizumab, using Pichia pastoris.
    Article Snippet: The development of anti-interleukin-6-receptor (IL6R) recombinant monoclonal antibody Tocilizumab (TCZ) production in a methylotrophic yeast Pichia pastoris was the focus of this research work.. The molecular weight of full-length TCZ is approximately 148 kDa.. A bicistronic expression vector with both heavy and light chain genes was constructed within individual inducible alcohol oxidase promoters and secretory signal peptides.

    Article Title: Labyrinthulid microorganism capable of producing microbial oil, microbial oil, methods for producing said microorganism and for producing said microbial oil, and uses of said microorganism and said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: After amplification with E. coli, the sequence was confirmed using a Dye Terminator Cycle Sequencing Kit (available from Beckman Coulter Inc.) (FIG. 58). .. A primer set that was set up in the reverse direction with the objective of deleting a portion of the C20 elongase gene sequence and inserting a BglII site (1939 bp, SEQ ID NO: 170) was prepared using the plasmid illustrated in FIG. 58 as a template, and the set was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Amplification:

    Article Title: Development of a novel system for the expression and production of recombinant monoclonal antibody, tocilizumab, using Pichia pastoris.
    Article Snippet: The development of anti-interleukin-6-receptor (IL6R) recombinant monoclonal antibody Tocilizumab (TCZ) production in a methylotrophic yeast Pichia pastoris was the focus of this research work.. The molecular weight of full-length TCZ is approximately 148 kDa.. A bicistronic expression vector with both heavy and light chain genes was constructed within individual inducible alcohol oxidase promoters and secretory signal peptides.

    Article Title: Labyrinthulid microorganism capable of producing microbial oil, microbial oil, methods for producing said microorganism and for producing said microbial oil, and uses of said microorganism and said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: After amplification with E. coli, the sequence was confirmed using a Dye Terminator Cycle Sequencing Kit (available from Beckman Coulter Inc.) (FIG. 58). .. A primer set that was set up in the reverse direction with the objective of deleting a portion of the C20 elongase gene sequence and inserting a BglII site (1939 bp, SEQ ID NO: 170) was prepared using the plasmid illustrated in FIG. 58 as a template, and the set was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Cloning:

    Article Title: Development of a novel system for the expression and production of recombinant monoclonal antibody, tocilizumab, using Pichia pastoris.
    Article Snippet: The development of anti-interleukin-6-receptor (IL6R) recombinant monoclonal antibody Tocilizumab (TCZ) production in a methylotrophic yeast Pichia pastoris was the focus of this research work.. The molecular weight of full-length TCZ is approximately 148 kDa.. A bicistronic expression vector with both heavy and light chain genes was constructed within individual inducible alcohol oxidase promoters and secretory signal peptides.

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    Clone Assay:

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction
    Article Snippet: .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction.
    Article Snippet: ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    Modification:

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction
    Article Snippet: .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction.
    Article Snippet: ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Polymerase Chain Reaction:

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction
    Article Snippet: .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction.
    Article Snippet: ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    In Vivo:

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction
    Article Snippet: .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Article Title: A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarction.
    Article Snippet: ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. .. ENPP1 (BstYI fragment from pIRES2-EGFP-ENPP1) was cloned into BglII site of pAcGFP-C1 (Clontech), while pIRES2-EGFP-ENPP5 was modified by PCR and subsequent bacterial in vivo assembly to remove ENPP5 stop codon and IRES2. ..

    Produced:

    Article Title: Labyrinthulid microorganism capable of producing microbial oil, microbial oil, methods for producing said microorganism and for producing said microbial oil, and uses of said microorganism and said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: .. A primer set that was set up in the reverse direction so as to insert a BglII site into the core portion of the C20 elongase gene sequence was prepared using pRH80 (FIG. 7) produced in Example 2-4 as a template, and the resultant was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..

    Construct:

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    CRISPR:

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    Synthesized:

    Article Title: Wdr59 promotes or inhibits TORC1 activity depending on cellular context
    Article Snippet: .. Mio3HF-F: TTCTAGGGTTAATACGTACTGTCCGGAGCACCCAC mio3HF-R: CCGGGATCCGATTACGTAATGGAAACCAGAAGCTGAAGC 3xGFP11-5xT7-Nprl2 gRNA construct: CRISPR targeting site: TCGCAGCCGTCTCATTCGTATGG Sense oligo: CTTCGTCGCAGCCGTCTCATTCGTA Antisense oligo: AAACTACGAATGAGACGGCTGCGAC Nprl2 5’ Homologous (HR) fragment cloning: Synthesized 1345 bps fragment containing 5’ Nprl2 homologues sequence and 3XGFP11-5xT7 were cloned into the EcoRV and BglII site of pUC57-3XGFP11piggy-5XGMR-3xp3-DtagRed via In-Fusion cloning (Takara) to obtain 5’ HR3XGFP11-5xT7-piggy-GMR-3xp3-TagRed construct. ..

    Plasmid Preparation:

    Article Title: Method for producing microbial oil from labyrinthulid microorganism capable of producing said microbial oil
    Article Snippet: After amplification with E. coli, the sequence was confirmed using a Dye Terminator Cycle Sequencing Kit (available from Beckman Coulter Inc.) (FIG. 58). .. A primer set that was set up in the reverse direction with the objective of deleting a portion of the C20 elongase gene sequence and inserting a BglII site (1939 bp, SEQ ID NO: 170) was prepared using the plasmid illustrated in FIG. 58 as a template, and the set was amplified with PrimeSTAR Max DNA Polymerase (available from Takara Bio Inc.). ..



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