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Citations for ChromoTek :
501 - 517 of 517 citations for Anti Neurogenin 1 Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Cell Biology 2022Quote: ... EGFP-INPP5E or its mutants were then immunoprecipitated from 1 mg of cell lysate by overnight rotation at 4°C with GFP-Trap_MA beads (Chromotek). Beads were then washed thrice in buffer containing 50mM Tris-HCl pH=7.5 and 150mM NaCl buffer (no protease inhibitors or detergent) ...
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bioRxiv - Cell Biology 2021Quote: ... 1 mg of lysate was incubated with 25 μL of equilibrated GFP-trap magnetic agarose beads (Chromotek, gtma-20) for 1 h with end-over-end rotation at 4 °C ...
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bioRxiv - Cell Biology 2020Quote: ... one step of O/N incubation at 4ºC with GFP booster (1:250, Alexa Fluor ® 488 Chromotek #gb2AF488), Phalloidin-647 (1:250 ...
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bioRxiv - Immunology 2021Quote: ... GFP-tagged PD-1 variants or BTLA variants were IP’ed from the lysate using GFP-Trap (Chromotek, #gta-20). Equal fractions of the IP samples were subjected to SDS-PAGE and blotted with indicated antibodies.
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bioRxiv - Cell Biology 2022Quote: ... MEFs were washed extensively and GFP-booster (tagged with Alexa488, ChromoTek, gb2AF488-50, 1:500 in 3%BSA/PBS) and anti-rabbit-Alexa568 (Invitrogen ...
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bioRxiv - Biophysics 2023Quote: ... 0.25 mM PMSF) and eluted with 4 × 1 mL 0.15 mg/mL (50 µM) 3 x FLAG peptide (Chromotek). The elutant was concentrated with Amico-4 (50k MWCO ...
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bioRxiv - Microbiology 2020Quote: ... The supernatant was then transferred in 900 μl aliquots to fresh Eppendorf tubes and incubated with gentle head-over-tail agitation for 2 h at 4°C with 30 μl of anti-RFP or control beads (Chromotek rtma-2 and bmab-20, respectively) that had been washed in 1x lysis buffer.
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bioRxiv - Biochemistry 2021Quote: ... Cells were blocked in 3% BSA in PBS-T for 30 min before incubation with GFP-Booster _Atto488 (1:300; Chromotek), or mouse anti-G3BP1 in 3% BSA in PBS-T for 1 h at room temperature ...
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bioRxiv - Evolutionary Biology 2022Quote: ... resuspended in 1 ml ice cold IPP150 buffer and subsequently processed using similar protocol as above with the following exceptions: 1/ supernatant was incubated with 50 μl of V5-Trap magnetic Particles M-270 (Chromotek, v5td-20 ...
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bioRxiv - Molecular Biology 2022Quote: ... on a rotating wheel at 4° C for 1 h in triplicates with GFP-Trap agarose beads (#gta-200, Chromotek) or control agarose beads (Chromotek) ...
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bioRxiv - Plant Biology 2023Quote: ... 1 mL of the protein supernatant was incubated with 10 μL of magnetic GFP-Trap beads (Chromotek, Cat. No. gtma) or magnetic Myc-Trap beads (Chromotek ...
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bioRxiv - Plant Biology 2024Quote: ... 1 mL of supernatant was incubated at 4°C for 2 h with GFP-Trap_A beads (Chromotek, Planegg-Martinsried, Germany). The beads were collected by centrifugation at 800 × g and washed four times in 1 mL washing buffer (25 mM Tris pH=7.5 ...
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bioRxiv - Cancer Biology 2024Quote: ... 1 mg of total lysate (in triplicate) was incubated with 35 µl of GFP-Trap_A agarose beads slurry (ChromoTek GmbH) for 2 h at 4°C with end-to-end rotation ...
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bioRxiv - Systems Biology 2021Quote: ... Protein concentration was evaluated with a BCA dosage and 1 mg of total protein was incubated at 4 °C for 4 hours with agarose GFP beads (ChromoTek, Germany) for PHB-GFP or with magnetic FLAG beads (Sigma ...
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bioRxiv - Plant Biology 2024Quote: Immunoprecipitation was performed by adding 1 g of homogenized leaf material 50 µL of GFP-Trap® coupled to magnetic beads (ChromoTek). Samples were processed as described (Raffeiner et al. ...
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bioRxiv - Plant Biology 2023Quote: ... Lysates were precleared with 50 µL of sepharose beads for 1 h at 4°C with constant rotation and subjected to immunoprecipitation with 25 µL GFP Trap agarose beads (Chromotek, gta-20) during 1 h at 4°C with constant rotation ...
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bioRxiv - Plant Biology 2024Quote: Co-immunoprecipitations of the GFP-tagged FtsZ2-1 line was performed in biological triplicates using GFP-Trap Magnetic Particles M-270 (Chromotek, Planegg-Martinsried, Germany). In brief ...