人 USF1 (NM_207005) cDNA克隆

基本信息

Accession: NM_207005
基因名称: USF1
基因别名: UEF; FCHL; MLTF; FCHL1; MLTFI; HYPLIP1; bHLHb11
基因描述: Homo sapiens upstream transcription factor 1 (USF1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 756 (查看编码区序列)
翻译后氨基酸长度: 251 (查看氨基酸序列)
Transcript Variant: This variant (2, also known as USF1/BD) uses an alternate splice site in its 5' UTR, and uses a downstream in-frame start codon, compared to variant 1. The encoded isoform (2) is shorter at the N-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G117748 人 USF1 (NM_207005) 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 USF1 (NM_007122) cDNA克隆 transcript variant 1
人 USF1 (NM_207005) cDNA克隆 transcript variant 2
人 USF1 (NM_001276373) cDNA克隆 transcript variant 3

基因简介

This gene encodes a member of the basic helix-loop-helix leucine zipper family, and can function as a cellular transcription factor. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs. This gene has been linked to familial combined hyperlipidemia (FCHL). Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been defined on chromosome 21. [provided by RefSeq, Feb 2013]

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