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USP1 encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. Zusätzlich bieten wir Ihnen USP1 Antikörper (95) und viele weitere Produktgruppen zu diesem Protein an.
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These results outline a novel mechanism for the control of TBK1 (zeige TBK1 Proteine) activity and suggest USP1-UAF1 (zeige WDR48 Proteine) complex as a potential target for the prevention of viral diseases.
USP1 is a key senescence regulator controlling genomic integrity.
High USP1 expression is associated with glioma.
USP1-UAF1 (zeige WDR48 Proteine) complex promotes homologous recombination repair via multiple mechanisms: through FANCD2 deubiquitination, as well as by interacting with RAD51AP1 (zeige RAD51AP1 Proteine).
The results suggest that silencing USP1 inhibits cell proliferation and invasion in U2OS cells. Therefore, USP1 may provide a novel therapeutic target for the treatment of osteosarcoma.
Translational regulation of the mRNA encoding USP1 is involved in the DNA damage response as a determinant of cisplatin resistance.
Ubiquitination-specific proteases 1 (USP1)-mediated protein stabilization promotes glioblastoma (GBM) stem-like cells maintenance and treatment resistance, thereby providing a rationale for USP1 inhibition as a potential therapeutic approach against GBM.
analysis of the function and regulation of the USP1-UAF1 (zeige WDR48 Proteine) complex
USP1, p21 and Spartan are translesion DNA synthesis regulators. (Review)
No correlation was observed between the protein level of ubiquitin-specific protease 1 (USP1) and ubiquitinated PCNA (zeige PCNA Proteine) in BAF180 (zeige PBRM1 Proteine) expressing cells
our results strongly suggest that Usp1 is involved in the regulation of centrosome duplication, at least in part via ID1 (zeige ID1 Proteine), and Usp1 may exert its oncogenic activity, partially through inducing centrosome abnormality.
Data suggest Usp1 down-regulation by autocleavage is critical for Usp1 to exert role in DNA interstrand crosslink repair; Usp1 role is de-ubiquitination of Fancd2 (Fanconi anemia complementation group D2) and Pcna (proliferating cell nuclear antigen (zeige PCNA Proteine)).
Homozygous Uaf1 (zeige WDR48 Proteine)(-/-) embryos died at embryonic day 7.5 (E7.5). These mutant embryos were small and developmentally retarded.
Autocleaved Usp1 remains a deubiquitylase because its fragments remain associated with Uaf1, an enhancer of Usp1 activity, until the C-terminal fragment is selectively destroyed by the Arg/N-end rule pathway.
Bone marrow from Fancd2-/- mice and Usp1-/- mice exhibited marked hematopoietic defects.
mouse Usp1 functions downstream in the Fanconi anemia pathway, and its deubiquitination is required for Fancd2 nuclear foci assembly
This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. The protein specifically deubiquitinates a protein in the Fanconi anemia (FA) DNA repair pathway. Alternate transcriptional splice variants have been characterized.
ubiquitin carboxyl-terminal hydrolase 1
, ubiquitin specific protease 1
, ubiquitin specific peptidase 1
, ubiquitin carboxyl-terminal hydrolase 1-like
, deubiquitinating enzyme 1
, ubiquitin carboxyl terminal hydrolase 1
, ubiquitin specific processing protease 1
, ubiquitin thioesterase 1
, ubiquitin thiolesterase 1
, ubiquitin-specific-processing protease 1
, ubiquitin specific peptdiase 1