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david chan  (Addgene inc)


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    Structured Review

    Addgene inc david chan
    David Chan, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pet28+mff+1+61+pp+gst/pET28-Mff(1-61)-PP-GST+(Plasmid+%2373042)/pmc12817251-589-7-9
    Average 94 stars, based on 4 article reviews
    david chan - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Construct:

    Article Title: Systematic histone H4 replacement in Arabidopsis thaliana reveals a role for H4R17 in regulating flowering time.
    Article Snippet: .. Constructs for the production of recombinant protein were generated as follows: Using the NdeI and BamHI restriction sites, the coding sequences of H4 (aa 1–30) were cloned into pET28-Mff(1-61)-PP-GST (Addgene plasmid #73042; provided by D. Chan) and fused with a C-terminal glutathione-S-transferase (GST) tag (Davarinejad et al., 2022). .. Site-directed mutagenesis was used to create the H4R17A mutation (QuikChange II XL, Agilent Technologies).

    Recombinant:

    Article Title: Systematic histone H4 replacement in Arabidopsis thaliana reveals a role for H4R17 in regulating flowering time.
    Article Snippet: .. Constructs for the production of recombinant protein were generated as follows: Using the NdeI and BamHI restriction sites, the coding sequences of H4 (aa 1–30) were cloned into pET28-Mff(1-61)-PP-GST (Addgene plasmid #73042; provided by D. Chan) and fused with a C-terminal glutathione-S-transferase (GST) tag (Davarinejad et al., 2022). .. Site-directed mutagenesis was used to create the H4R17A mutation (QuikChange II XL, Agilent Technologies).

    Generated:

    Article Title: Systematic histone H4 replacement in Arabidopsis thaliana reveals a role for H4R17 in regulating flowering time.
    Article Snippet: .. Constructs for the production of recombinant protein were generated as follows: Using the NdeI and BamHI restriction sites, the coding sequences of H4 (aa 1–30) were cloned into pET28-Mff(1-61)-PP-GST (Addgene plasmid #73042; provided by D. Chan) and fused with a C-terminal glutathione-S-transferase (GST) tag (Davarinejad et al., 2022). .. Site-directed mutagenesis was used to create the H4R17A mutation (QuikChange II XL, Agilent Technologies).

    Clone Assay:

    Article Title: Systematic histone H4 replacement in Arabidopsis thaliana reveals a role for H4R17 in regulating flowering time.
    Article Snippet: .. Constructs for the production of recombinant protein were generated as follows: Using the NdeI and BamHI restriction sites, the coding sequences of H4 (aa 1–30) were cloned into pET28-Mff(1-61)-PP-GST (Addgene plasmid #73042; provided by D. Chan) and fused with a C-terminal glutathione-S-transferase (GST) tag (Davarinejad et al., 2022). .. Site-directed mutagenesis was used to create the H4R17A mutation (QuikChange II XL, Agilent Technologies).

    Plasmid Preparation:

    Article Title: Systematic histone H4 replacement in Arabidopsis thaliana reveals a role for H4R17 in regulating flowering time.
    Article Snippet: .. Constructs for the production of recombinant protein were generated as follows: Using the NdeI and BamHI restriction sites, the coding sequences of H4 (aa 1–30) were cloned into pET28-Mff(1-61)-PP-GST (Addgene plasmid #73042; provided by D. Chan) and fused with a C-terminal glutathione-S-transferase (GST) tag (Davarinejad et al., 2022). .. Site-directed mutagenesis was used to create the H4R17A mutation (QuikChange II XL, Agilent Technologies).



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    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: SAYSD1 senses UFMylated ribosome to safeguard co-translational protein translocation at the endoplasmic reticulum

    doi: 10.1016/j.celrep.2023.112028

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: To generate GST-fusion proteins, the corresponding DNA fragments encoding different domains of SAYSD1 were either inserted into the pET41a vector to construct N-terminal GST fusion proteins or used to replace Mff(1–61) in the pET28-Mff(1–61)-PP-GST vector (Addgene #73042) to generate C-terminal GST-fusion proteins.

    Techniques: Virus, Recombinant, Ubiquitin Proteomics, Enzyme-linked Immunosorbent Assay, Negative Control, Software