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penta mutant sortase a esrta  (Addgene inc)


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    Structured Review

    Addgene inc penta mutant sortase a esrta
    Penta Mutant Sortase A Esrta, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 69 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sortase+a/sortase+A+pentamutant+(eSrtA)+in+pET29+(Plasmid+%2375144)/bio_rxiv__64898__2026__03__09__710718-213-2-11
    Average 94 stars, based on 69 article reviews
    penta mutant sortase a esrta - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Generated:

    Article Title: A Conditionally Activated Cytosol-Penetrating Antibody for TME-Dependent Intracellular Cargo Delivery
    Article Snippet: Excess fluorescent dye was removed using ZebaTM Spin Desalting Columns, 7K MWCO (Thermo Fisher Science). .. Antibody toxin conjugates were generated by an enzyme-mediated coupling reaction using a penta-mutated variant of sortase A [ ] [eSrtA in pET29 (Addgene plasmid: # 75144)] [ ]. ..

    Variant Assay:

    Article Title: A Conditionally Activated Cytosol-Penetrating Antibody for TME-Dependent Intracellular Cargo Delivery
    Article Snippet: Excess fluorescent dye was removed using ZebaTM Spin Desalting Columns, 7K MWCO (Thermo Fisher Science). .. Antibody toxin conjugates were generated by an enzyme-mediated coupling reaction using a penta-mutated variant of sortase A [ ] [eSrtA in pET29 (Addgene plasmid: # 75144)] [ ]. ..

    Article Title: Tumor-specific Cytosol-Penetrating Antibodies for Antigen- and TME-Dependent Intracellular Cargo Delivery
    Article Snippet: .. 545 Jo urn al Pr e-p roo f 22 Protein Coupling 546 In order to facilitate protein-protein coupling utilizing sortase A, a penta-mutant variant of 547 sortase A 66 [eSrtA in pET29 (Addgene plasmid: # 75144)] 67 was employed. ..

    Article Title: Tumor-specific cytosol-penetrating antibodies for antigen- and TME-dependent intracellular cargo delivery
    Article Snippet: .. In order to facilitate protein-protein coupling utilizing sortase A, a penta-mutant variant of sortase A (eSrtA in pET29 [Addgene plasmid: # 75144]) was employed. ..

    Plasmid Preparation:

    Article Title: A Conditionally Activated Cytosol-Penetrating Antibody for TME-Dependent Intracellular Cargo Delivery
    Article Snippet: Excess fluorescent dye was removed using ZebaTM Spin Desalting Columns, 7K MWCO (Thermo Fisher Science). .. Antibody toxin conjugates were generated by an enzyme-mediated coupling reaction using a penta-mutated variant of sortase A [ ] [eSrtA in pET29 (Addgene plasmid: # 75144)] [ ]. ..

    Article Title: Deep mutational scanning highlights a role for cytosolic regions in Hrd1 function
    Article Snippet: TEV, purified in house , This paper , Addgene plasmid # 8827 ; http://n2t.net/addgene:8827 ; RRID:Addgene_8827. .. Sortase A, purified in house , This paper , Addgene plasmid # 75144 ; http://n2t.net/addgene:75144 ; RRID:Addgene_75144. .. BeadBeater , BioSpec , Cat#1107900-105.

    Article Title: Morphodynamics of human early brain organoid development.
    Article Snippet: .. Sortase A (SrtA; plasmid #75144, Addgene) with a 6×-His tag was expressed in E. coli BL21(DE3) following a published protocol61. ..

    Article Title: Morphodynamics of human early brain organoid development
    Article Snippet: .. Sortase A (SrtA; plasmid #75144, Addgene) with a 6×-His tag was expressed in E. coli BL21(DE3) following a published protocol . ..

    Article Title: Tumor-specific Cytosol-Penetrating Antibodies for Antigen- and TME-Dependent Intracellular Cargo Delivery
    Article Snippet: .. 545 Jo urn al Pr e-p roo f 22 Protein Coupling 546 In order to facilitate protein-protein coupling utilizing sortase A, a penta-mutant variant of 547 sortase A 66 [eSrtA in pET29 (Addgene plasmid: # 75144)] 67 was employed. ..

    Article Title: Tumor-specific cytosol-penetrating antibodies for antigen- and TME-dependent intracellular cargo delivery
    Article Snippet: .. In order to facilitate protein-protein coupling utilizing sortase A, a penta-mutant variant of sortase A (eSrtA in pET29 [Addgene plasmid: # 75144]) was employed. ..

    Ligation:

    Article Title: BrainBike peptidomimetic enables efficient transport of proteins across brain endothelium
    Article Snippet: .. Sortase A ligation of the BCN linker to the scFv Once the antibody was produced, the reaction with Sortase A (SrtA, BPS Bioscience Catalog #71046, or in-house produced from Addgene Catalog #75144) to remove the His-tag and incorporate the BCN linker (Gly-PEG3-endo-BCN, BroadPharm, Catalog #BP-24232) was performed. ..

    Produced:

    Article Title: BrainBike peptidomimetic enables efficient transport of proteins across brain endothelium
    Article Snippet: .. Sortase A ligation of the BCN linker to the scFv Once the antibody was produced, the reaction with Sortase A (SrtA, BPS Bioscience Catalog #71046, or in-house produced from Addgene Catalog #75144) to remove the His-tag and incorporate the BCN linker (Gly-PEG3-endo-BCN, BroadPharm, Catalog #BP-24232) was performed. ..

    Purification:

    Article Title: Deep mutational scanning highlights a role for cytosolic regions in Hrd1 function
    Article Snippet: TEV, purified in house , This paper , Addgene plasmid # 8827 ; http://n2t.net/addgene:8827 ; RRID:Addgene_8827. .. Sortase A, purified in house , This paper , Addgene plasmid # 75144 ; http://n2t.net/addgene:75144 ; RRID:Addgene_75144. .. BeadBeater , BioSpec , Cat#1107900-105.



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    Image Search Results


    Hyperin reduces biofilm formation, adhesion and cytotoxicity. ( a ) The absorbance at 600 nm of S. aureus USA300 when it was cocultured with various concentrations of hyperin. ( b ) Biofilm formation of S. aureus USA300 after treatment with different concentrations of hyperin. S. aureus USA300 was cultured with different concentrations of hyperin for 24 h, the samples were stained with 0.2% crystal violet, and the absorbance at 570 nm was measured after treatment with 35% glacial acetic acid. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( c ) Adhesion of S. aureus USA300 to lung epithelial cells when different concentrations of hyperin were added. A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 1.5 h, after which the cells were washed, harvested, plated onto LB agar medium and cultured. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( d ) Survival rate of A549 cells treated with hyperin. The data are shown as the mean and SD. ( e ) LDH levels in A549 cells and the survival of cells determined by live/dead staining ( f ). A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 6 h. The LDH levels in the supernatant were measured with an LDH kit, and the cells were stained with live/dead reagents. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. The bar represents 50 μm. ( g ) The expression levels of SrtA and ClfA in S. aureus USA300 treated with different concentrations of hyperin. S. aureus USA300 was cocultured with different concentrations of hyperin, after which the bacteria were harvested by centrifugation and treated with SDS-PAGE loading buffer. The proteins were separated on a 10% gel and identified by specific antibodies. ( h ) Quantitative analysis of the expression levels of SrtA and ClfA ( i ). The analysis was performed with Image J 1.54 g. The data are shown as the mean and SD.** indicates p ≤ 0.01.

    Journal: Scientific Reports

    Article Title: inhibitory effect of hyperin on Staphylococcus aureus pathogenicity though interactions with sortase A and sortase B

    doi: 10.1038/s41598-025-23458-1

    Figure Lengend Snippet: Hyperin reduces biofilm formation, adhesion and cytotoxicity. ( a ) The absorbance at 600 nm of S. aureus USA300 when it was cocultured with various concentrations of hyperin. ( b ) Biofilm formation of S. aureus USA300 after treatment with different concentrations of hyperin. S. aureus USA300 was cultured with different concentrations of hyperin for 24 h, the samples were stained with 0.2% crystal violet, and the absorbance at 570 nm was measured after treatment with 35% glacial acetic acid. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( c ) Adhesion of S. aureus USA300 to lung epithelial cells when different concentrations of hyperin were added. A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 1.5 h, after which the cells were washed, harvested, plated onto LB agar medium and cultured. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( d ) Survival rate of A549 cells treated with hyperin. The data are shown as the mean and SD. ( e ) LDH levels in A549 cells and the survival of cells determined by live/dead staining ( f ). A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 6 h. The LDH levels in the supernatant were measured with an LDH kit, and the cells were stained with live/dead reagents. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. The bar represents 50 μm. ( g ) The expression levels of SrtA and ClfA in S. aureus USA300 treated with different concentrations of hyperin. S. aureus USA300 was cocultured with different concentrations of hyperin, after which the bacteria were harvested by centrifugation and treated with SDS-PAGE loading buffer. The proteins were separated on a 10% gel and identified by specific antibodies. ( h ) Quantitative analysis of the expression levels of SrtA and ClfA ( i ). The analysis was performed with Image J 1.54 g. The data are shown as the mean and SD.** indicates p ≤ 0.01.

    Article Snippet: ClfA antibody (Cusabio, CSB-PA692021ZA01FLB, 1:1000), and SrtA antibody (cusabio, CSB-EP3093FLF, 1:3000).

    Techniques: Cell Culture, Staining, Expressing, Bacteria, Centrifugation, SDS Page

    Hyperin reduces biofilm formation, adhesion and cytotoxicity. ( a ) The absorbance at 600 nm of S. aureus USA300 when it was cocultured with various concentrations of hyperin. ( b ) Biofilm formation of S. aureus USA300 after treatment with different concentrations of hyperin. S. aureus USA300 was cultured with different concentrations of hyperin for 24 h, the samples were stained with 0.2% crystal violet, and the absorbance at 570 nm was measured after treatment with 35% glacial acetic acid. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( c ) Adhesion of S. aureus USA300 to lung epithelial cells when different concentrations of hyperin were added. A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 1.5 h, after which the cells were washed, harvested, plated onto LB agar medium and cultured. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( d ) Survival rate of A549 cells treated with hyperin. The data are shown as the mean and SD. ( e ) LDH levels in A549 cells and the survival of cells determined by live/dead staining ( f ). A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 6 h. The LDH levels in the supernatant were measured with an LDH kit, and the cells were stained with live/dead reagents. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. The bar represents 50 μm. ( g ) The expression levels of SrtA and ClfA in S. aureus USA300 treated with different concentrations of hyperin. S. aureus USA300 was cocultured with different concentrations of hyperin, after which the bacteria were harvested by centrifugation and treated with SDS-PAGE loading buffer. The proteins were separated on a 10% gel and identified by specific antibodies. ( h ) Quantitative analysis of the expression levels of SrtA and ClfA ( i ). The analysis was performed with Image J 1.54 g. The data are shown as the mean and SD.** indicates p ≤ 0.01.

    Journal: Scientific Reports

    Article Title: inhibitory effect of hyperin on Staphylococcus aureus pathogenicity though interactions with sortase A and sortase B

    doi: 10.1038/s41598-025-23458-1

    Figure Lengend Snippet: Hyperin reduces biofilm formation, adhesion and cytotoxicity. ( a ) The absorbance at 600 nm of S. aureus USA300 when it was cocultured with various concentrations of hyperin. ( b ) Biofilm formation of S. aureus USA300 after treatment with different concentrations of hyperin. S. aureus USA300 was cultured with different concentrations of hyperin for 24 h, the samples were stained with 0.2% crystal violet, and the absorbance at 570 nm was measured after treatment with 35% glacial acetic acid. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( c ) Adhesion of S. aureus USA300 to lung epithelial cells when different concentrations of hyperin were added. A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 1.5 h, after which the cells were washed, harvested, plated onto LB agar medium and cultured. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. ( d ) Survival rate of A549 cells treated with hyperin. The data are shown as the mean and SD. ( e ) LDH levels in A549 cells and the survival of cells determined by live/dead staining ( f ). A549 cells were treated with S. aureus USA300 and different concentrations of hyperin for 6 h. The LDH levels in the supernatant were measured with an LDH kit, and the cells were stained with live/dead reagents. Data are shown as the mean with the SD, ** indicates p ≤ 0.01. The bar represents 50 μm. ( g ) The expression levels of SrtA and ClfA in S. aureus USA300 treated with different concentrations of hyperin. S. aureus USA300 was cocultured with different concentrations of hyperin, after which the bacteria were harvested by centrifugation and treated with SDS-PAGE loading buffer. The proteins were separated on a 10% gel and identified by specific antibodies. ( h ) Quantitative analysis of the expression levels of SrtA and ClfA ( i ). The analysis was performed with Image J 1.54 g. The data are shown as the mean and SD.** indicates p ≤ 0.01.

    Article Snippet: ClfA antibody (Cusabio, CSB-PA692021ZA01FLB, 1:1000), and SrtA antibody (cusabio, CSB-EP3093FLF, 1:3000).

    Techniques: Cell Culture, Staining, Expressing, Bacteria, Centrifugation, SDS Page