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UFD1
Ubiquitin recognition factor in ER associated degradation 1UFD1L
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. [provided by RefSeq, Jun 2009]
Top validated antibodies |
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| Proteintech Group |  10615-1-AP |
9 references | Polyclonal |
WB
EL
ICC
IP
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| Invitrogen Antibodies | 10615-1-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
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| Novus Biologicals | NBP2-61829 |
Monoclonal |
WB
EL
ICC
IHC
FC
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| antibodies-online | ABIN4881128 |
Monoclonal |
WB
EL
ICC
IHC
FC
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| NovoPro Bioscience Inc. | 116551 |
Polyclonal |
WB
EL
ICC
IP
IHC
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