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atp sulfurylase  (R&D Systems)


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    Structured Review

    R&D Systems atp sulfurylase
    Atp Sulfurylase, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/atp+sulfurylase/Recombinant+S%2E+cerevisiae+ATP+Sulfurylase%2FMET3+Protein%2C+CF/pmc13017612-109-31-36
    Average 94 stars, based on 3 article reviews
    atp sulfurylase - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: ENPP1 enzyme replacement therapy improves ectopic calcification but does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia
    Article Snippet: .. A standard curve was created by spiking with known concentrations of PPi (Santa Cruz Biotechnology, Dallas, TX) in water, and 15 μL of filtered plasma samples were mixed with 5 μL of assay buffer (40 mM HEPES pH 7.4, 8 mM CaCl 2 , 2 mM MgSO 4 ) containing 16 μM adenosine 5 ́-phosphosulfate (Sigma-Aldrich, St. Louis, MO), 0.1 U/mL ATP sulfurylase (R&D Systems, Minneapolis, MN). ..

    Concentration Assay:

    Article Title: Highly Ordered DNA Framework Interface Enables Efficient Enzymatic Oligonucleotide Synthesis.
    Article Snippet: .. The reaction buffer (100 mm Tris acetate, 0.5 mm EDTA, 5 mmmagnesium acetate, and 0.01% v/v Tween 20, pH 7.6) was prepared at a 2× concentration, including 2 ng μL−1 ATP sulfurylase (7175-AS, R&D Systems), 10 μm adenosine phosphosulfate (APS, A5508, Sigma–Aldrich), 0.24 μg/μL firefly luciferase (FL0001, MCLAB), and 1.2 μg μL−1 D-luciferin (L9504, Sigma–Aldrich). ..

    Article Title: Supporting Information for DNA-DISK: automated end-to-end data storage via enzymatic single- nucleotide DNA synthesis and sequencing on digital microfluidics
    Article Snippet: SSB binding buffer was composed of pyrosequencing washing buffer with 0.48 μg/μL SSB (ESSB, MCLAB). .. Substrate-enzymatic reaction buffer was prepared at a 2× concentration and contained washing buffer with 1 U/μL Klenow fragment of DNA polymerase (M0210, NEB), 2 ng/μL ATP sulfurylase (7175-AS, R&D Systems), 10 μM adenosine phosphosulfate (APS, A5508, Sigma-Aldrich), 2 mM dithiothreitol (DTT), 0.24 μg/μL SSB and 20 μM of one of the four nucleotides, dATP-α-S (orb64011, Biorbyt), dTTP, dCTP or dGTP (P035-37, Vazyme). .. Chemiluminescence reaction buffer was prepared at a 2× concentration as well and contained washing buffer with 0.24 μg/μL firefly luciferase (FL0001, MCLAB) and 1.2 μg/μL Dluciferin (L9504, Sigma-Aldrich).

    Article Title: Supporting Information for DNA-DISK: automated end-to-end data storage via enzymatic single- nucleotide DNA synthesis and sequencing on digital microfluidics
    Article Snippet: Apyrasewashing buffer was made by mixing the aforementioned washing buffer with 20 mU/mL apyrase (M0398, NEB). .. Substrate-enzymatic reaction buffer at a 2× concentration and was prepared by mixing washing buffer with 1 U/μL Klenow fragment of DNA polymerase (M0210, NEB), 2 ng/μL ATP sulfurylase (7175-AS, R&D Systems), 10 μM adenosine phosphosulfate (APS, A5508, SigmaAldrich), 2 mM dithiothreitol (DTT), 0.24 μg/μL SSB and 20 μM of one of the four nucleotides, dATPα-S (orb64011, Biorbyt), dTTP, dCTP or dGTP (P035-37, Vazyme). .. Chemiluminescence reaction buffer was prepared at a 2× concentration as well and was made by mixing washing buffer with 0.24 μg/μL firefly luciferase (FL0001, MCLAB) and 1.2 μg/μL D-luciferin (L9504, Sigma-Aldrich).

    Article Title: Highly Ordered DNA Framework Interface Enables Efficient Enzymatic Oligonucleotide Synthesis
    Article Snippet: .. The reaction buffer (100 m m Tris acetate, 0.5 m m EDTA, 5 m m magnesium acetate, and 0.01% v/v Tween 20, pH 7.6) was prepared at a 2× concentration, including 2 ng μL −1 ATP sulfurylase (7175‐AS, R&D Systems), 10 μ m adenosine phosphosulfate (APS, A5508, Sigma–Aldrich), 0.24 μg/μL firefly luciferase (FL0001, MCLAB), and 1.2 μg μL −1 D‐luciferin (L9504, Sigma–Aldrich). ..

    Luciferase:

    Article Title: Highly Ordered DNA Framework Interface Enables Efficient Enzymatic Oligonucleotide Synthesis.
    Article Snippet: .. The reaction buffer (100 mm Tris acetate, 0.5 mm EDTA, 5 mmmagnesium acetate, and 0.01% v/v Tween 20, pH 7.6) was prepared at a 2× concentration, including 2 ng μL−1 ATP sulfurylase (7175-AS, R&D Systems), 10 μm adenosine phosphosulfate (APS, A5508, Sigma–Aldrich), 0.24 μg/μL firefly luciferase (FL0001, MCLAB), and 1.2 μg μL−1 D-luciferin (L9504, Sigma–Aldrich). ..

    Article Title: Highly Ordered DNA Framework Interface Enables Efficient Enzymatic Oligonucleotide Synthesis
    Article Snippet: .. The reaction buffer (100 m m Tris acetate, 0.5 m m EDTA, 5 m m magnesium acetate, and 0.01% v/v Tween 20, pH 7.6) was prepared at a 2× concentration, including 2 ng μL −1 ATP sulfurylase (7175‐AS, R&D Systems), 10 μ m adenosine phosphosulfate (APS, A5508, Sigma–Aldrich), 0.24 μg/μL firefly luciferase (FL0001, MCLAB), and 1.2 μg μL −1 D‐luciferin (L9504, Sigma–Aldrich). ..



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