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Citations for Molecular Cloning Laboratory :
1 - 9 of 9 citations for Prestained Protein Standards since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Microbiology 2020Quote: ... in the presence of Red DNA Size Standard (Molecular Cloning Laboratories, USA). The set of fluorescent dyes used in this work appeared to be suboptimal because of the need to check data for issues of spectral overlapping between TAMRA and ROX channels.
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bioRxiv - Bioengineering 2022Quote: ... LwaCas13a proteins were purchased from MCLAB (cat# CAS13a-100). Cas13a and crRNA were mixed in 1×PBS to form the non-activated Cas13a/crRNA at room temperature for 20 min and stored at -80°C ...
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bioRxiv - Molecular Biology 2020Quote: ... The protein biosensors were purified by Ni-NTA agarose (MCLAB) and the TBS buffer was exchanged into MOPS buffer using 10 kDa ultrafiltration tubes (Amicon).
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bioRxiv - Biochemistry 2020Quote: ... the protein complex was purified by affinity chromatography (Ni-NTA Agarose, MCLAB), anion-exchange (Source Q ...
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bioRxiv - Biochemistry 2020Quote: ... the proteins were purified using immobilized metal affinity chromatography (Ni-NTA agarose, MCLAB) and then anion-exchange chromatography (Source Q ...
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Impact of DNA sequences in the DNA duplex opening by the Rad4/XPC nucleotide excision repair complexbioRxiv - Biochemistry 2020Quote: ... the proteins were purified using immobilized metal affinity chromatography (Ni-NTA agarose, MCLAB) and then anion-exchange chromatography (Source Q ...
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bioRxiv - Microbiology 2022Quote: ... Fractions containing the desired protein were pooled and mixed with SUMO Protease (MCLAB, CA, USA) with the provided SUMO buffer (salt-free) ...
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bioRxiv - Biophysics 2021Quote: ... The fusion protein was subsequently digested with His-tagged SUMO protease (McLab, South San Francisco, CA) at 4 °C for 1–2 h to remove the SUMO tag and the resulting cleavage mixture was then passed through Ni-NTA resin column ...
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bioRxiv - Synthetic Biology 2023Quote: ... All sensor and ligand proteins except for SH2 were purified by nickel-nitrilotriacetate chromatography according to the manufacturer’s instructions (Molecular Cloning Laboratories). SH2 did not have a His-Tag and was purified using an SP Sepharose column as described37 ...