mProX™ Human PRLHR Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 Prlhr localizes to cilia in the hypothalamic third ventricle.
In the adult mouse brain, Prlhr was confined to the ventricular cilium. An anti-Prlhr antibody (green) was used to immunostain frozen slices of the adult mouse brain that included the third ventricle. In cilia sticking out from cells on the third ventricle's surface, the Prlhr signal was seen.
Ref: Omori, Yoshihiro, et al. "Identification of G protein-coupled receptors (GPCRs) in primary cilia and their possible involvement in body weight control." PloS one 10.6 (2015): e0128422.
Pubmed: 26053317
DOI: 10.1371/journal.pone.0128422
Research Highlights
A helpful biomarker for determining the prognosis and effectiveness of immune checkpoint inhibitors (ICIs) is tumor mutation burden (TMB). A novel therapeutic target for the treatment of glioma patients and an increase in their survival rate may be provided by PRLHR, which may act as a tumor suppressor for the growth of the disease.
Liu, Yi, et al. "PRLHR Immune Genes Associated With Tumor Mutation Burden can be Used as Prognostic Markers in Patients With Gliomas." Frontiers in Oncology 12 (2022): 620190.
Pubmed:
35800054
DOI:
10.3389/fonc.2022.620190
The investigation of the spectrum of PRL, PRLR, and PRLHR gene variations in women of reproductive age with nontumor hyperprolactinemia was the main objective of the study. PRL, PRLR, and PRLHR genes underwent targeted high throughput sequencing in women with hyperprolactinemia of nontumor etiology.
Shakhtshneider, E. V., et al. "Results of Targeted Sequencing of PRL, PRLR, and PRLHR Genes in Young Women with Nonneoplastic Hyperprolactinemia." Cell and Tissue Biology 17.3 (2023): 292-298.