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Cambridge Isotope Laboratories c8 atp
C8 Atp, supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/c8+atp/pmc10462655-230-10-35
Average 93 stars, based on 1 article reviews
c8 atp - by Bioz Stars, 2026-09
93/100 stars

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Synthesized:

Article Title: Dynamically regulated two-site interaction of viral RNA to capture host translation initiation factor
Article Snippet: .. The [{1′, 2′, 3′, 4′, 5′, 5′′}- 2 H, 13 C8] ATP was enzymatically synthesized by using D-[1, 2, 3, 4, 5, 5′- 2 H 6 ] ribose (Omicron Biochemicals RIB-040) and 13 C8 adenine (Cambridge Isotope Laboratories CLM-1654-PK) as substrates, with the dATP regeneration system . .. In the reaction, in-house purified RK, PRPPS, and APRT were used, in addition to creatine kinase from rabbit muscle (CK, Roche 10127566001), myokinase from rabbit muscle (MK, Sigma-Aldrich M3003), and thermostable inorganic pyrophosphatase (TIPP, New England Biolabs M0296L).



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A Coomassie Brilliant Blue-stained SDS-PAGE of <t>purified</t> <t>BSEP</t> solubilized in Fos-choline-16 or in β-DDM and Cymal5, which were exchanged after solubilization. Molecular weight markers are indicated on the left. B Purified BSEP in all three detergents was incubated with <t>ATP-agarose</t> and bound protein was eluted in SDS sample buffer and examined with immunoblotting with a monoclonal antibody (F-6). BSEP signals could be detected in β-DDM and Cymal5, but not in Fos-Choline-16, indicating only binding to ATP in maltosides.
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A Coomassie Brilliant Blue-stained SDS-PAGE of <t>purified</t> <t>BSEP</t> solubilized in Fos-choline-16 or in β-DDM and Cymal5, which were exchanged after solubilization. Molecular weight markers are indicated on the left. B Purified BSEP in all three detergents was incubated with <t>ATP-agarose</t> and bound protein was eluted in SDS sample buffer and examined with immunoblotting with a monoclonal antibody (F-6). BSEP signals could be detected in β-DDM and Cymal5, but not in Fos-Choline-16, indicating only binding to ATP in maltosides.
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A Coomassie Brilliant Blue-stained SDS-PAGE of <t>purified</t> <t>BSEP</t> solubilized in Fos-choline-16 or in β-DDM and Cymal5, which were exchanged after solubilization. Molecular weight markers are indicated on the left. B Purified BSEP in all three detergents was incubated with <t>ATP-agarose</t> and bound protein was eluted in SDS sample buffer and examined with immunoblotting with a monoclonal antibody (F-6). BSEP signals could be detected in β-DDM and Cymal5, but not in Fos-Choline-16, indicating only binding to ATP in maltosides.
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A Coomassie Brilliant Blue-stained SDS-PAGE of purified BSEP solubilized in Fos-choline-16 or in β-DDM and Cymal5, which were exchanged after solubilization. Molecular weight markers are indicated on the left. B Purified BSEP in all three detergents was incubated with ATP-agarose and bound protein was eluted in SDS sample buffer and examined with immunoblotting with a monoclonal antibody (F-6). BSEP signals could be detected in β-DDM and Cymal5, but not in Fos-Choline-16, indicating only binding to ATP in maltosides.

Journal: PLoS ONE

Article Title: Detergent Screening and Purification of the Human Liver ABC Transporters BSEP (ABCB11) and MDR3 (ABCB4) Expressed in the Yeast Pichia pastoris

doi: 10.1371/journal.pone.0060620

Figure Lengend Snippet: A Coomassie Brilliant Blue-stained SDS-PAGE of purified BSEP solubilized in Fos-choline-16 or in β-DDM and Cymal5, which were exchanged after solubilization. Molecular weight markers are indicated on the left. B Purified BSEP in all three detergents was incubated with ATP-agarose and bound protein was eluted in SDS sample buffer and examined with immunoblotting with a monoclonal antibody (F-6). BSEP signals could be detected in β-DDM and Cymal5, but not in Fos-Choline-16, indicating only binding to ATP in maltosides.

Article Snippet: To test the ability of detergent solubilized BSEP to bind ATP, 25 µl of a 1∶1 slurry of C8-linked ATP-agarose resin (Sigma) equilibrated in buffer A was added to 20 µg of purified BSEP in the detergent to be examined and incubated at 4°C on a rotator.

Techniques: Staining, SDS Page, Purification, Molecular Weight, Incubation, Western Blot, Binding Assay