人 NSFL1C (NM_018839) cDNA克隆

基本信息

Accession: NM_018839
基因名称: NSFL1C
基因别名: P47; UBX1; UBXD10; UBXN2C; dJ776F14.1
基因描述: Homo sapiens NSFL1 (p97) cofactor (p47) (NSFL1C), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1020 (查看编码区序列)
翻译后氨基酸长度: 339 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate in-frame exon in the central coding region, compared to variant 1, resulting in an isoform (b) that is shorter than isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G110353 人 NSFL1C (NM_018839) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 NSFL1C (NM_016143) cDNA克隆 transcript variant 1
人 NSFL1C (NM_018839) cDNA克隆 transcript variant 2
人 NSFL1C (NM_001206736) cDNA克隆 transcript variant 4

基因简介

N-ethylmaleimide-sensitive factor (NSF) and valosin-containing protein (p97) are two ATPases known to be involved in transport vesicle/target membrane fusion and fusions between membrane compartments. A trimer of the protein encoded by this gene binds a hexamer of cytosolic p97 and is required for p97-mediated regrowth of Golgi cisternae from mitotic Golgi fragments. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, May 2011]

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