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golden gate assembly kit  (New England Biolabs)


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    New England Biolabs golden gate assembly kit
    Golden Gate Assembly Kit, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 324 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/golden+gate+assembly+kit/NEBridge+Golden+Gate+Assembly+Kit/pm42754924-51-28-27
    Average 99 stars, based on 324 article reviews
    golden gate assembly kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Amplification:

    Article Title: β-Carbonic anhydrases integrate CO 2 and light cues to coordinate photosynthesis in tomato.
    Article Snippet: Optimization of photosynthesis requires precise coordination between electron transport and CO2 assimilation, but how plants maintain this coordination under suboptimal CO2 and light conditions remains poorly understood.. Here, we identify two tomato (Solanum lycopersicum) b-carbonic anhydrases (bCAs) responsive to deficient CO2.. Although both are required for biomass accumulation and efficient photosynthesis, the chloroplast bCA1 does not directly participate in carbon assimilation but instead specifically coordinates photosystem performance and leaf internal structure.

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISPRn library was cloned into lentiGuide-Puro (Addgene, cat. no. 52963) using NEBuilder HiFi DNA Assembly Master Mix (New England Biolabs, cat. no. E2621L) according to manufacturer specifications. .. The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2).

    Clone Assay:

    Article Title: β-Carbonic anhydrases integrate CO 2 and light cues to coordinate photosynthesis in tomato.
    Article Snippet: Optimization of photosynthesis requires precise coordination between electron transport and CO2 assimilation, but how plants maintain this coordination under suboptimal CO2 and light conditions remains poorly understood.. Here, we identify two tomato (Solanum lycopersicum) b-carbonic anhydrases (bCAs) responsive to deficient CO2.. Although both are required for biomass accumulation and efficient photosynthesis, the chloroplast bCA1 does not directly participate in carbon assimilation but instead specifically coordinates photosystem performance and leaf internal structure.

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISPRn library was cloned into lentiGuide-Puro (Addgene, cat. no. 52963) using NEBuilder HiFi DNA Assembly Master Mix (New England Biolabs, cat. no. E2621L) according to manufacturer specifications. .. The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2).

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2). .. Single gRNAs for arrayed CRISPRn validations were ordered as crRNAs (Horizon Discovery) for CRISPR RNP-based nucleofection.

    Plasmid Preparation:

    Article Title: β-Carbonic anhydrases integrate CO 2 and light cues to coordinate photosynthesis in tomato.
    Article Snippet: Optimization of photosynthesis requires precise coordination between electron transport and CO2 assimilation, but how plants maintain this coordination under suboptimal CO2 and light conditions remains poorly understood.. Here, we identify two tomato (Solanum lycopersicum) b-carbonic anhydrases (bCAs) responsive to deficient CO2.. Although both are required for biomass accumulation and efficient photosynthesis, the chloroplast bCA1 does not directly participate in carbon assimilation but instead specifically coordinates photosystem performance and leaf internal structure.

    Article Title: Parallel CLE peptide signaling pathways control nodulation in pea
    Article Snippet: .. PsCLE12 and PsCLE13 under the control of a CAMV35S promoter were inserted in the pCAMBIA_CR1 (pCR1) vector that contains the DsRED transformation marker (Sevin-Pujol et al., 2017) using the Golden Gate Assembly Kit (New England Biolabs, Ipswich, MA, USA). .. PCR fragments for these genes were generated from pea root cDNA using primers containing the BsaI recognition site and matching overhangs (Table S1), following the manufacturer’s instructions and transferred into ARqua1 Agrobacterium rhizogenes. pCR1::CAMV35S::GUS plasmid or pCR1:: CASP ::GUS was used as a control.

    Article Title: Techno-economic assessment-guided biofoundry for microbial strain development.
    Article Snippet: Yu Been Heo, Sung Cheon Ko, Jay D. Keasling, Han Min Woo hmwoo@skku.edu (H.M.. Woo).. Trends in Biotechnology, Month 2025, Vol. xx, No. xx https://doi.org/10.1016/j.tibtech.2025.11.002 TIBTEC 2849 No. of Pages 24 Trends in Biotechnology

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2). .. Single gRNAs for arrayed CRISPRn validations were ordered as crRNAs (Horizon Discovery) for CRISPR RNP-based nucleofection.

    Polymerase Chain Reaction:

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISPRn library was cloned into lentiGuide-Puro (Addgene, cat. no. 52963) using NEBuilder HiFi DNA Assembly Master Mix (New England Biolabs, cat. no. E2621L) according to manufacturer specifications. .. The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2).

    Control:

    Article Title: Parallel CLE peptide signaling pathways control nodulation in pea
    Article Snippet: .. PsCLE12 and PsCLE13 under the control of a CAMV35S promoter were inserted in the pCAMBIA_CR1 (pCR1) vector that contains the DsRED transformation marker (Sevin-Pujol et al., 2017) using the Golden Gate Assembly Kit (New England Biolabs, Ipswich, MA, USA). .. PCR fragments for these genes were generated from pea root cDNA using primers containing the BsaI recognition site and matching overhangs (Table S1), following the manufacturer’s instructions and transferred into ARqua1 Agrobacterium rhizogenes. pCR1::CAMV35S::GUS plasmid or pCR1:: CASP ::GUS was used as a control.

    Transformation Assay:

    Article Title: Parallel CLE peptide signaling pathways control nodulation in pea
    Article Snippet: .. PsCLE12 and PsCLE13 under the control of a CAMV35S promoter were inserted in the pCAMBIA_CR1 (pCR1) vector that contains the DsRED transformation marker (Sevin-Pujol et al., 2017) using the Golden Gate Assembly Kit (New England Biolabs, Ipswich, MA, USA). .. PCR fragments for these genes were generated from pea root cDNA using primers containing the BsaI recognition site and matching overhangs (Table S1), following the manufacturer’s instructions and transferred into ARqua1 Agrobacterium rhizogenes. pCR1::CAMV35S::GUS plasmid or pCR1:: CASP ::GUS was used as a control.

    Marker:

    Article Title: Parallel CLE peptide signaling pathways control nodulation in pea
    Article Snippet: .. PsCLE12 and PsCLE13 under the control of a CAMV35S promoter were inserted in the pCAMBIA_CR1 (pCR1) vector that contains the DsRED transformation marker (Sevin-Pujol et al., 2017) using the Golden Gate Assembly Kit (New England Biolabs, Ipswich, MA, USA). .. PCR fragments for these genes were generated from pea root cDNA using primers containing the BsaI recognition site and matching overhangs (Table S1), following the manufacturer’s instructions and transferred into ARqua1 Agrobacterium rhizogenes. pCR1::CAMV35S::GUS plasmid or pCR1:: CASP ::GUS was used as a control.

    Construct:

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2). .. Single gRNAs for arrayed CRISPRn validations were ordered as crRNAs (Horizon Discovery) for CRISPR RNP-based nucleofection.

    Article Title: Assessment of the phi6 lysis system using genetic complementation and heterologous expression in Escherichia coli and Pseudomonas syringae
    Article Snippet: .. The pJLC140 shuttle vector was constructed using the Golden Gate assembly kit (BsaI, NEB #E1601L) following the manufacturer’s recommended protocols. .. Assembly involved combining three synthetic DNA gBlocks with an amplicon generated from the pJH1 vector ( ) (Addgene #154204) using primers 653 and 652.

    Cloning:

    Article Title: Systematic discovery of pro- and anti-HIV host factors in primary human CD4+ T cells.
    Article Snippet: The secondary CRISRPa library was amplified by PCR (15 cycles) with golden gate compatible primers and cloned into pXPR_502 (Addgene, cat. no. 96923) using NEB Golden Gate Assembly Kit (BsmBI-v2, New England Biolabs, cat. no. E1602L) following the manufacturer’s protocol. .. Individual sgRNAs for arrayed CRISPRa validations were constructed by Golden Gate Cloning as described in.86 Briefly, DNA oligomers with Golden Gate overhangs were annealed and cloned into a non-digested target plasmid, pXPR_502, using the NEB Golden Gate Assembly Kit (BsmBI-v2). .. Single gRNAs for arrayed CRISPRn validations were ordered as crRNAs (Horizon Discovery) for CRISPR RNP-based nucleofection.

    Concentration Assay:

    Article Title: Systematic genome-wide mapping of host determinants of bacteriophage infectivity
    Article Snippet: PCR was performed using KAPA HiFi (Roche KK2101) for all experiments, except for colony PCR, where KAPA2G Robust (Roche KK5005) was utilized. .. The New England Biosciences (NEB) Golden Gate Assembly Kit (BsaI-HF v2, E1601L) and the Gibson Assembly Protocol (NEB E5510) were employed, utilizing our in-house-prepared Gibson Assembly Master Mix (final concentration 100mM Tris-HCl pH 7.5, 20mM MgCl2, 0.2mM dATP/dCTP/dGTP/dTTP, 10mM DTT, 5% PEG-8000, 1mM NAD+, 4U/ml T5 exonuclease, 4U/μl Taq DNA ligase, 25U/ml Phusion polymerase). .. PCR was performed using KAPA HiFi (Roche KK2101) for all experiments, except for colony PCR, where KAPA2G Robust (Roche KK5005) was utilized.



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