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人 C9orf78 抗体对
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人 C9orf78 抗体对

01AB02130

Chromosome 9 open reading frame 78 (C9orf78) is a human protein involved in the late-stage regulation of pre-mRNA splicing. It functions by interacting with the spliceosome remodeling enzyme SNRNP200 (BRR2), binding to its coiled-coil domain to moderately inhibit helicase activity on U4/U6 di-snRNA. This interaction facilitates spliceosome maturation and influences 3'-splice site selection. C9orf78 also binds to U5 snRNA and displaces WBP4 from the SNRNP200 complex, ensuring proper alternative splicing patterns. Beyond its role in the spliceosome, C9orf78 interacts with FAM50A to upregulate the expression of asparagine synthetase (ASNS). This pathway is clinically significant in oncology, as the FAM50A-C9orf78 axis has been shown to enhance the migration, invasion, and brain metastasis of breast cancer cells. Consequently, C9orf78 is recognized as a key factor in promoting aggressive tumor phenotypes and metastatic progression.

Human
规格起售价
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技术参数

靶点基因名
C9orf78
基因别名
HCA59
蛋白别名
chromosome 9 open reading frame 78; C9orf78
UniProt
Q9NZ63
物种
Human

产品详情

靶点名称
C9orf78
蛋白名称
chromosome 9 open reading frame 78
蛋白别名
Splicing factor C9orf78; Hepatocellular carcinoma-associated antigen 59
靶点基因名
C9orf78
基因别名
HCA59
UniProt
Q9NZ63
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Chromosome 9 open reading frame 78 (C9orf78) is a human protein involved in the late-stage regulation of pre-mRNA splicing. It functions by interacting with the spliceosome remodeling enzyme SNRNP200 (BRR2), binding to its coiled-coil domain to moderately inhibit helicase activity on U4/U6 di-snRNA. This interaction facilitates spliceosome maturation and influences 3'-splice site selection. C9orf78 also binds to U5 snRNA and displaces WBP4 from the SNRNP200 complex, ensuring proper alternative splicing patterns. Beyond its role in the spliceosome, C9orf78 interacts with FAM50A to upregulate the expression of asparagine synthetase (ASNS). This pathway is clinically significant in oncology, as the FAM50A-C9orf78 axis has been shown to enhance the migration, invasion, and brain metastasis of breast cancer cells. Consequently, C9orf78 is recognized as a key factor in promoting aggressive tumor phenotypes and metastatic progression.