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UFD1L 产品

(Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

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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].

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Featured UFD1L Categories

UFD1L 抗体

High quality antibodies with extensive validation data.

UFD1L 蛋白

Proteins for various applications incl. WB, ELISA, IF etc.

Recommended UFD1L 抗体

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Cat. No. ABIN2856688
Quantity 100 μL
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Application WB, IHC, ELISA, ICC, FACS
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Cat. No. ABIN5542401
Quantity 100 μL
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Application WB, IHC, ELISA, ICC, FACS
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Cat. No. ABIN5542400
Quantity 100 μL
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Recommended UFD1L 蛋白

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Cat. No. ABIN7125585
Quantity 50 μg
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Source Wheat germ
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Cat. No. ABIN1324547
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Cat. No. ABIN1324549
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Latest Publications for our UFD1L Products

Guo, Qi: "VCP cooperates with UBXD1 to degrade mitochondrial outer membrane protein MCL1 in model of Huntington's disease." in: Biochimica et biophysica acta, Vol. 1863, Issue 2, pp. 552-559, (2016) (PubMed).

Nagahama, Suzuki, Hamada, Hatsuzawa, Tani, Yamamoto, Tagaya: "SVIP is a novel VCP/p97-interacting protein whose expression causes cell vacuolation." in: Molecular biology of the cell, Vol. 14, Issue 1, pp. 262-73, (2003) (PubMed).

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, Vol. 19, Issue 10, pp. 2181-92, (2000) (PubMed).

Yamagishi, Garg, Matsuoka, Thomas, Srivastava: "A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects." in: Science (New York, N.Y.), Vol. 283, Issue 5405, pp. 1158-61, (1999) (PubMed).

Pizzuti, Novelli, Ratti, Amati, Mari, Calabrese, Nicolis, Silani, Marino, Scarlato, Ottolenghi, Dallapiccola: "UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome." in: Human molecular genetics, Vol. 6, Issue 2, pp. 259-65, (1997) (PubMed).

Synonyms and alternative names related to UFD1L

ubiquitin recognition factor in ER associated degradation 1 (UFD1), ubiquitin recognition factor in ER-associated degradation 1 (Ufd1), ubiquitin recognition factor in ER associated degradation 1 (Ufd1), ubiquitin fusion degradation 1 like (yeast) (UFD1L), ubiquitin recognition factor in ER associated degradation 1 S homeolog (ufd1.S), ubiquitin recognition factor in ER associated degradation 1 (ufd1l), ubiquitin recognition factor in ER associated degradation 1 (ufd1), ubiquitin fusion degradation protein 1 homolog (EHI_125920), ubiquitin fusion degradation protein 1 homolog (LOC100166745), ubiquitin fusion degradation protein 1 homolog (LOC100635687), ubiquitin fusion degradation protein 1 homolog (LOC100648660), Ubiquitin Fusion Degradation (yeast UFD homolog) (ufd-1), UFD1, Ufd1, ufd1, Ufd1l, wu:fc55f04, zgc:92341

Protein level used designations for UFD1L

  • UB fusion protein 1
  • ubiquitin fusion degradation protein 1 homolog
  • ubiquitin fusion degradation 1-like protein
  • fc55f04
  • ubiquitin fusion degradation 1-like
  • ubiquitin fusion degradation 1 like (yeast)
  • ubiquitin fusion degradation 1 like
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