CTU2 (formerly known as C16orf84) is a human gene located on chromosome 16.[5] The mRNA encodes the longer isoform. The gene encodes a cytoplasmic protein that plays a probable role in tRNA modification.
Background References
1. Shaheen R et al. Biallelic variants in CTU2 cause DREAM-PL syndrome and impair thiolation of tRNA wobble U34. Hum Mutat. 2019 Nov
cytosolic thiouridylase subunit 2 homolog (S. pombe) antibody
NCS2 antibody
PF0432 antibody
Images
Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-CTU2 antibody (HA722086) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA722086) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Western blot analysis of CTU2 on different lysates with Rabbit anti-CTU2 antibody (HA722086) at 1/2,000 dilution.
Lane 1: HeLa cell lysate Lane 2: HT-29 cell lysate Lane 3: 293T cell lysate Lane 4: K-562 cell lysate Lane 5: Raji cell lysate Lane 6: HepG2 cell lysate Lane 7: COS-1 cell lysate Lane 8: NIH/3T3 cell lysate Lane 9: Mouse spleen tissue lysate
Lysates/proteins at 30 µg/Lane. Exposure time: 24 seconds; ECL: K1801
Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: HA722086, 1/2,000 in 5% NFDM/TBST, overnight at 4 ℃ Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature
Predicted band size: 56 kDa Observed band size: 56 kDa
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