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人 HLTF 抗体对
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人 HLTF 抗体对

01AB03186

Helicase-like transcription factor (HLTF) is a multifunctional DNA translocase of the SWI/SNF family, possessing ATP-dependent helicase and E3 ubiquitin ligase activities. It contains a HIRAN domain for recognizing DNA structures, a SWI/SNF-type ATPase domain, and a RING finger domain. HLTF is critical for genome stability, functioning as the human homolog of yeast RAD5 in error-free post-replication repair. It is recruited to stalled replication forks, where it polyubiquitinates PCNA and promotes fork reversal, facilitating DNA damage tolerance. In oncology, HLTF acts as a tumor suppressor; its promoter is frequently hypermethylated in colorectal and gastric cancers, and its inactivation leads to genomic instability and altered sensitivity to DNA-damaging agents.

Human
规格起售价
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技术参数

靶点基因名
HLTF
基因别名
HIP116A; RNF80; SMARCA3; SNF2L3; ZBU1
蛋白别名
helicase like transcription factor; HLTF
UniProt
Q14527
物种
Human

产品详情

靶点名称
HLTF
蛋白名称
helicase like transcription factor
蛋白别名
Helicase-like transcription factor; DNA-binding protein/plasminogen activator inhibitor 1 regulator; HIP116; RING finger protein 80; RING-type E3 ubiquitin transferase HLTF; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 3; Sucrose nonfermenting protein 2-like 3
靶点基因名
HLTF
基因别名
HIP116A; RNF80; SMARCA3; SNF2L3; ZBU1
UniProt
Q14527
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Helicase-like transcription factor (HLTF) is a multifunctional DNA translocase of the SWI/SNF family, possessing ATP-dependent helicase and E3 ubiquitin ligase activities. It contains a HIRAN domain for recognizing DNA structures, a SWI/SNF-type ATPase domain, and a RING finger domain. HLTF is critical for genome stability, functioning as the human homolog of yeast RAD5 in error-free post-replication repair. It is recruited to stalled replication forks, where it polyubiquitinates PCNA and promotes fork reversal, facilitating DNA damage tolerance. In oncology, HLTF acts as a tumor suppressor; its promoter is frequently hypermethylated in colorectal and gastric cancers, and its inactivation leads to genomic instability and altered sensitivity to DNA-damaging agents.