- Peptide Substrates
- Binding Proteins
- Secondary Antibodies
- Regulatory proteins
- 脂类激酶
- 双加氧酶与蛋白质
- 脂质底物
- E2
- Assay Buffer and Co-factors
- Methyltransferases
- Acetyltransferases
- Transcription Proteins
- COVID-19 ELISA Kits
- Tau Proteins
- Microtubule & Actin Associated Proteins
- Carbohydrate Substrates
- COVID-19 Proteins
- Chemokines
- 标记抗体
- 授予称号
- E3
Overview:
The transcription factor Aryl hydrocarbon receptor nuclear translocator (ARNT), alternatively named Hypoxia-inducible factor (HIF)-1β, is part of the Hypoxia-inducible factor (HIF) pathway which mediates cellular adaptations to hypoxia and promotes tumour progression. Unlike HIF-1α that is regulated in an oxygen-dependent manner, HIF-1β is constitutively expressed. It has been shown that some tumour cells are capable to elevate HIF-1β in response to hypoxia to for a clonal advantage. HIF-1β binds HIF-1α, and forms the transcriptional active HIF-1 complex in the nucleus.
Gene Aliases:
ARNT; bHLHe2; HIF-1-beta; HIF-1beta; HIF1-beta; HIF1BETA; TANGO
Genbank Number:
NM_001668
References:
1. Mandl M, et al: (2015). The expression level of the transcription factor Aryl hydrocarbon receptor nuclear translocator (ARNT) determines cellular survival after radiation treatment. Radiat Oncol. 16;10:229.2. Mandl M, et al (2013): Hypoxia-inducible factor-1β (HIF-1β) is upregulated in a HIF-1α-dependent manner in 518A2 human melanoma cells under hypoxic conditions. Biochem Biophys Res Commun. 26;434(1):166-72.