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The protein encoded by UFD1L forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. Additionally we are shipping Ubiquitin Fusion Degradation Protein 1 Homolog Proteins (9) and Ubiquitin Fusion Degradation Protein 1 Homolog Kits (1) and many more products for this protein.
Showing 10 out of 94 products:
Human Monoclonal UFD1L Primary Antibody for IF, WB - ABIN968620
Meyer, Shorter, Seemann, Pappin, Warren: A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways. in The EMBO journal 2000
Show all 4 Pubmed References
Human Polyclonal UFD1L Primary Antibody for IP, WB - ABIN315864
Guo, Qi: VCP cooperates with UBXD1 to degrade mitochondrial outer membrane protein MCL1 in model of Huntington's disease. in Biochimica et biophysica acta 2016
These findings identified a role for CDC-48(UFD-1/NPL-4) in DNA replication, which is important for cell cycle progression and genome stability.
The study revealed a regulatory role of the p97 (show EIF4G2 Antibodies)-Npl4-Ufd1 complex in regulating a partial degradation of the NF-kappaB (show NFKB1 Antibodies) subunit p100 (show PATL2 Antibodies).
the p97-Ufd1-Npl4 complex couples ubiquitinated IP(3) receptors to proteasomal degradation and, thus, plays a key role in IP(3) receptor processing
structural analysis of the p97 (show EIF4G2 Antibodies)-Npl4-Ufd1 interface
The study revealed a regulatory role of the p97 (show EIF4G2 Antibodies)-Npl4-Ufd1 complex in regulating a partial degradation of the NF-kappaB (show NFKB1 Antibodies) subunit p100 (show CUX1 Antibodies).
p97-Ufd1-Npl4 is an integral part of G2/M checkpoint signaling and thereby suppresses chromosome instability.
Data indicate that the p97-UFD1L-NPL4 protein complex specifically associates with ubiquitinated IkappaBalpha via the interactions between p97 and the SCF(beta-TRCP) ubiquitin ligase.
This study demonistrated that UFD1L may participate in the core cognitive deficits observed in schizophrenia.
In coordination with the P97 (show EIF4G2 Antibodies)-UFD1-NPL4 complex (P97 (show EIF4G2 Antibodies)(UFD1/NPL4)), NUB1L promotes transfer of NEDD8 (show NEDD8 Antibodies) to proteasome for degradation.
increased corpus callosum volume in children with 22q11DS is associated with UFD1L polymorphism.
Data indicate that Npl4-Ufd1 heterodimer is required for VCP (show vcp Antibodies)-FAF1 (show FAF1 Antibodies) interaction.
Data establish Cdc48/p97 (show vcp Antibodies)-Ufd1-Npl4 as a crucial negative regulator of Aurora B (show AURKB Antibodies) early in mitosis of human somatic cells and suggest that the activity of Aurora B (show AURKB Antibodies) on chromosomes needs to be restrained to ensure faithful chromosome segregation.
Ubiquitin-recognition protein Ufd1 couples the endoplasmic reticulum (ER) stress response to cell cycle control
This study suggested that AA genotype of UFD1L gene, which is involved in neurodevelopmental processes, may contribute to early-onset schizophrenia. Therefore, rs5992403 polymorphism may not be a risk factor for schizophrenia.
The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18.
ubiquitin fusion degradation protein 1 homolog
, ubiquitin fusion degradation 1-like protein
, ubiquitin fusion degradation 1-like
, ubiquitin fusion degradation 1 like (yeast)
, UB fusion protein 1