Review



sapi mediated golden gate assembly  (New England Biolabs)


Bioz Verified Symbol New England Biolabs is a verified supplier
Bioz Manufacturer Symbol New England Biolabs manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 96
      Buy from Supplier

    Structured Review

    New England Biolabs sapi mediated golden gate assembly
    A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using <t>pooled</t> <t>SapI-mediated</t> Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.
    Sapi Mediated Golden Gate Assembly, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 934 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sapi mediated golden gate assembly/product/New England Biolabs
    Average 96 stars, based on 934 article reviews
    sapi mediated golden gate assembly - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "A whole organism screening platform identifies gut microbiome microproteins that modulate host metabolism"

    Article Title: A whole organism screening platform identifies gut microbiome microproteins that modulate host metabolism

    Journal: bioRxiv

    doi: 10.64898/2026.02.11.705328

    A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using pooled SapI-mediated Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.
    Figure Legend Snippet: A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using pooled SapI-mediated Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.

    Techniques Used: Derivative Assay, Clone Assay, Expressing, Plasmid Preparation, Transformation Assay, Positive Control, Mutagenesis, Produced, Bacteria, Control



    Similar Products

    sapi mediated golden gate assembly  (New England Biolabs)
    96
    New England Biolabs sapi mediated golden gate assembly
    A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using <t>pooled</t> <t>SapI-mediated</t> Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.
    Sapi Mediated Golden Gate Assembly, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sapi mediated golden gate assembly/product/New England Biolabs
    Average 96 stars, based on 1 article reviews
    sapi mediated golden gate assembly - by Bioz Stars, 2026-03
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using pooled SapI-mediated Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.

    Journal: bioRxiv

    Article Title: A whole organism screening platform identifies gut microbiome microproteins that modulate host metabolism

    doi: 10.64898/2026.02.11.705328

    Figure Lengend Snippet: A . A diverse 236-member library of gut-derived putative secreted microproteins was shortlisted via bioinformatics. From an existing dataset of microbial smORFs , those derived from gut metagenomic samples and predicted to be secreted were selected. Removal of redundant sequences resulted in a list of 2,412 total proteins. Representatives from each microprotein family were chosen to maximise protein diversity B . The smORF library was synthesised as an oligo pool, cloned into a pET9a expression vector using pooled SapI-mediated Golden Gate Assembly, then transformed into E. coli Lemo21. Positive control strains expressing the nematicidal toxin Cry6A and a reduced-function mutation, Cry6Am, were also produced. The resulting cloned expression library was arrayed into 96-well microplates, which included strains expressing 126 unique microproteins. To screen, bacteria were grown as lawns and Day 1 adult C. elegans N2 worms were allowed to crawl freely across the lawn. After 4 hours of exposure, worm behaviour was recorded for ∼16 minutes and quantified using a semi-automated worm tracking and statistical analysis pipeline. C . Hierarchical clustering of worm behavioural fingerprints in response to control, Cry6A, or Cry6Am exposure. Number of replicate wells screened: Cry6A_a: 43; Cry6A_b: 159; Cry6Am_a: 49; Cry6Am_b: 104; Control_a: 47; Control_b: 264. Each column corresponds to an individual feature from the Tierpsy 48 feature set, and each row shows the average Z-normalised feature value for that feature across all replicate wells of given condition. Rows were clustered using average linkage hierarchical clustering with Euclidian distance computed across all features of the matrix. Columns are coloured based on whether the feature name contains one of the key words listed below the heatmap. Rows are coloured according to the experimental condition.

    Article Snippet: The purified PCR products (Monarch PCR and DNA Cleanup Kit, New England Biolabs) were cloned into pET9a_linker using SapI-mediated Golden Gate Assembly (New England Biolabs), and the resulting plasmids were transformed into E. coli Lemo21 and plated onto chloramphenicol/kanamycin selection plates.

    Techniques: Derivative Assay, Clone Assay, Expressing, Plasmid Preparation, Transformation Assay, Positive Control, Mutagenesis, Produced, Bacteria, Control