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人 KDM3A 抗体对
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人 KDM3A 抗体对

01AB04071

Lysine demethylase 3A (KDM3A), also known as JMJD1A, is a histone demethylase that specifically targets mono- and dimethylated lysine 9 on histone H3, playing a crucial role in gene expression regulation and transcriptional activation, particularly in hormone-dependent pathways. KDM3A is implicated in various biological processes, including spermatogenesis and metabolic regulation, contributing to obesity resistance by modulating genes such as PPARα and UCP1. Dysregulation of KDM3A has been associated with several diseases, notably cancer; it facilitates chemoresistance and cancer stemness by demethylating key proteins like p53, thereby inhibiting apoptotic pathways. Additionally, KDM3A's overexpression is linked to prostate cancer progression through its interaction with androgen receptors and hypoxia-inducible factors, making it a potential therapeutic target for cancer treatment.

Human
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技术参数

靶点基因名
KDM3A
基因别名
JHDM2A; JMJD1; JMJD1A; KIAA0742; TSGA
蛋白别名
lysine demethylase 3A; KDM3A
UniProt
Q9Y4C1
物种
Human

产品详情

靶点名称
KDM3A
蛋白名称
lysine demethylase 3A
蛋白别名
Lysine-specific demethylase 3A; JmjC domain-containing histone demethylation protein 2A; Jumonji domain-containing protein 1A; [histone H3]-dimethyl-L-lysine(9) demethylase 3A
靶点基因名
KDM3A
基因别名
JHDM2A; JMJD1; JMJD1A; KIAA0742; TSGA
UniProt
Q9Y4C1
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Lysine demethylase 3A (KDM3A), also known as JMJD1A, is a histone demethylase that specifically targets mono- and dimethylated lysine 9 on histone H3, playing a crucial role in gene expression regulation and transcriptional activation, particularly in hormone-dependent pathways. KDM3A is implicated in various biological processes, including spermatogenesis and metabolic regulation, contributing to obesity resistance by modulating genes such as PPARα and UCP1. Dysregulation of KDM3A has been associated with several diseases, notably cancer; it facilitates chemoresistance and cancer stemness by demethylating key proteins like p53, thereby inhibiting apoptotic pathways. Additionally, KDM3A's overexpression is linked to prostate cancer progression through its interaction with androgen receptors and hypoxia-inducible factors, making it a potential therapeutic target for cancer treatment.