Anti-Thyroid Hormone Receptor beta antibody - N-terminal
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Rabbit Polyclonal Thyroid Hormone Receptor beta antibody. N-terminal. Suitable for WB and reacts with Human, Mouse samples. Immunogen corresponding to Recombinant Fragment Protein within Human THRB.
View Alternative Names
ERBA2, NR1A2, THR1, THRB, Thyroid hormone receptor beta, Nuclear receptor subfamily 1 group A member 2, c-erbA-2, c-erbA-beta
- WB
Supplier Data
Western blot - Anti-Thyroid Hormone Receptor beta antibody - N-terminal (AB196484)
All lanes:
Western blot - Anti-Thyroid Hormone Receptor beta antibody - N-terminal (ab196484) at 1/500 dilution
Lane 1:
K562 cell extract
Lane 2:
PC3 cell extract
Lane 3:
HepG2 cell extract
Lane 4:
U251 cell extract
Lane 5:
Mouse liver tissue extract
Lane 6:
Mouse craniofacial tissue extract
Predicted band size: 52 kDa
false
Reactivity data
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Shipped at conditions
Appropriate short-term storage duration
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This receptor regulates critical metabolic processes and plays a role in development. THRB functions as part of a larger receptor complex partnering with retinoid X receptor (RXR) to form a heterodimer. This dimer binds to thyroid hormone response elements (TREs) on DNA modulating the expression of genes involved in metabolism thermogenesis and development of the central nervous system. The receptor's activity impacts many key physiological functions ensuring proper growth and metabolic balance.
Pathways
THRB engages significantly in the thyroid hormone signaling pathway and the lipid degradation pathway. It interacts with proteins like the aforementioned RXR in promoting transcriptional activities. In its regulatory capacity THRB helps facilitate lipid metabolism cholesterol homeostasis and energy management. As part of the thyroid hormone signaling pathway it controls numerous genes aligning with proteins like thyroid peroxidase (TPO) which in turn affect hormone synthesis.
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