硕肯生物硕肯生物Soken.bio
查看试用产品 →开放浏览 · 登录后申请
人 CTSV 抗体对
试剂盒

人 CTSV 抗体对

01AB01091

Cathepsin V (CTSV), also known as cathepsin L2 or cathepsin U, is a lysosomal cysteine protease belonging to the papain-like protease family (MEROPS family C1) and exhibits endopeptidase activity, primarily functioning in protein degradation within lysosomes. CTSV is notable for its non-canonical localization to the nucleus, where it regulates cell cycle progression and histone stability by modulating the levels of histones H3 and H4 and their chaperone sNASP, highlighting its roles beyond traditional proteolysis. The protein is expressed in various tissues and is upregulated in certain cancers, such as colorectal and breast carcinomas, but not in corresponding normal tissues, suggesting a role in tumorigenesis. Clinically, CTSV has been implicated in the progression of bladder cancer via activation of the NF-κB pathway and may contribute to the pathogenesis of keratoconus.

Human
规格起售价
登录后可查看

技术参数

靶点基因名
CTSV
基因别名
CATL2; CTSL2; CTSU
蛋白别名
cathepsin V; CTSV
UniProt
O60911
物种
Human

产品详情

靶点名称
CTSV
蛋白名称
cathepsin V
蛋白别名
Cathepsin L2; Cathepsin U; Cathepsin V
靶点基因名
CTSV
基因别名
CATL2; CTSL2; CTSU
UniProt
O60911
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Cathepsin V (CTSV), also known as cathepsin L2 or cathepsin U, is a lysosomal cysteine protease belonging to the papain-like protease family (MEROPS family C1) and exhibits endopeptidase activity, primarily functioning in protein degradation within lysosomes. CTSV is notable for its non-canonical localization to the nucleus, where it regulates cell cycle progression and histone stability by modulating the levels of histones H3 and H4 and their chaperone sNASP, highlighting its roles beyond traditional proteolysis. The protein is expressed in various tissues and is upregulated in certain cancers, such as colorectal and breast carcinomas, but not in corresponding normal tissues, suggesting a role in tumorigenesis. Clinically, CTSV has been implicated in the progression of bladder cancer via activation of the NF-κB pathway and may contribute to the pathogenesis of keratoconus.