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Citations for Boston Biochem :
1 - 9 of 9 citations for Angiotensin II receptor AT 2R Rabbit Polyclonal affinity purified since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Microbiology 2022Quote: ... Purified tetra-K63 ubiquitin was purchased from Boston Biochem. The following reagents were added to 20μl reactions where indicated ...
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bioRxiv - Molecular Biology 2019Quote: Purified xlCRL4CSA was neddylated in vitro using the NEDD8 Conjugation Initiation Kit (Boston Biochem) according to the manufacturer’s protocols ...
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bioRxiv - Cell Biology 2019Quote: ... ii) mock or 0.4 mg/ml of one of the following unlabled Ubiqutin variants: WT (Boston Biochem; #U100-H), Lys11 to Arg mutant (Boston Biochem ...
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bioRxiv - Microbiology 2023Quote: ... purified proteasome (1 nM final concentration) was activated with PA28 (12nM final concentration; E380 Boston Biochem) followed by addition of Boc-LRR-AMC (50 µM final concentration ...
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bioRxiv - Synthetic Biology 2021Quote: Ubiquitination assays were performed as previously described 45 in the presence of 0.1 μM purified human UBE1 (Boston Biochem), 4 μM human UbcH5α/UBE2D1 (Boston Biochem) ...
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bioRxiv - Cell Biology 2021Quote: ... the bait GST or GST fusion protein was incubated with purified human 26S proteasome (E365; Boston Biochem, Cambridge, MA, USA) at 4 °C for 2 h in binding buffer (1× PBS ...
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bioRxiv - Genetics 2020Quote: ... equal amounts of wild type OTUD5 or indicated OTUD5 mutants (purified as described above) were incubated with 0.5 μM K48- or K63-tetra ubiquitin chains (Boston Biochem) in cleavage buffer (110 mM potassium acetate ...
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bioRxiv - Immunology 2019Quote: ... coli was added to 2 µg of K48-ubiquitin chains of mixed chain length (Ub2-Ub7) or to purified tetra-ubiquitin (Ub4) (#UC-230, UC-210, Boston Biochem). A20 OTU domains added to mixed-length K48-ubiquitin chains were incubated in 100 µl of deubiquitin buffer (50 mM HEPES pH 8.0 ...
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bioRxiv - Biochemistry 2021Quote: ... Peptidase activities of purified immunoproteasomes were assayed using fluorogenic peptide substrates Ac-ANW-AMC for PSMB8 and Ac-PAL-AMC for PSMB9 (Boston Biochem). The measured activity was normalized against total protein concentration ...