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UFD1 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN1480
产品名称
UFD1 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
UFD1L
蛋白名称
Ubiquitin fusion degradation protein 1 homolog (UB fusion protein 1)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
7353
Human Swissprot No.
Q92890
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q92890/entry
Mouse Swissprot No.
P70362
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P70362
Rat Swissprot No.
Q9ES53
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941Q9ES53
免疫原
Synthesized peptide derived from part region of human protein
特异性
UFD1 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
33kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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],
组织表达
Found in adult heart, skeletal muscle and pancreas, and in fetal liver and kidney.
细胞定位
Nucleus . Cytoplasm, cytosol .
功能
caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:UFD1L gene hemizygosity is the cause of some of the catch 22-associated developmental defects whose notable examples are the DiGeorge syndrome (DGS), the velo-cardio-facial syndrome (VCFS) and the Opitz G/BBB syndrome.,function:Essential component of the ubiquitin-dependent proteolytic pathway which degrades ubiquitin fusion proteins. The ternary complex containing UFD1L, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope. It may be involved in the development of some ectoderm-derived structures.,pathway:Protein degradation; proteasomal ubiquitin-dependent pathway.,similarity:Belongs to the UFD1 family.,subunit:Heterodimer with NPLOC4, this heterodimer binds VCP and inhibits Golgi membrane fusion.,tissue specificity:Found in adult heart, skeletal muscle and pancreas, and in fetal liver and kidney.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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