Sheep Steroidogenic acute regulatory protein ELISA, StAR
- Known as:
- Sheep Steroidogenic acute regulatory protein Enzyme-linked immunosorbent assay test, StAR
- Catalog number:
- E14S0208
- Product Quantity:
- 96 Tests/kit
- Category:
- -
- Supplier:
- BGene
- Gene target:
- Sheep Steroidogenic acute regulatory protein ELISA StAR
Related genes to: Sheep Steroidogenic acute regulatory protein ELISA, StAR
- Gene:
- STAR NIH gene
- Name:
- steroidogenic acute regulatory protein
- Previous symbol:
- -
- Synonyms:
- StAR, STARD1
- Chromosome:
- 8p11.23
- Locus Type:
- gene with protein product
- Date approved:
- 1996-04-24
- Date modifiied:
- 2016-10-05
Related products to: Sheep Steroidogenic acute regulatory protein ELISA, StAR
Related articles to: Sheep Steroidogenic acute regulatory protein ELISA, StAR
- Advancements in additive manufacturing (AM) have created a strong demand for the qualification of metal alloys used in critical structural components. Ultrasound offers a promising non-destructive technique for analyzing mechanical properties from the complex and diverse microstructural features of AM materials. Targeting the physical mechanism from ultrasound to mechanical properties, we introduce a quantitative measure of microstructural inhomogeneity derived from parameterizing microstructural features. This inhomogeneity by inducing strain localization and the subsequent accumulation of geometrically necessary dislocations (GNDs), governs the material deformation. We demonstrate that this same inhomogeneity parameter also indicates the degree of ultrasonic attenuation. This establishes a direct, physical link between the elastodynamic response (attenuation) and the core plastic mechanism (GND accumulation), which ultimately determines material strength. Furthermore, we show numerically that the same inhomogeneity descriptor governs ultrasonic attenuation across materials belonging to different crystal systems, and we validate experimentally its effectiveness in predicting the relative strength of LPBF-fabricated SS316L, SS17-4PH and pure titanium. The full mechanistic chain linking attenuation to GND accumulation is established experimentally for LPBF SS316L, while its extension to other crystal systems is supported by simulation and requires material-specific calibration. These findings reveal the physical mechanism underlying the experimentally observed correlation between ultrasonic attenuation and mechanical strength in AM materials, enabling new framework for ultrasonic applications and enhancing the safety and reliability of AM alloys in critical structural components. - Source: PubMed
Publication date: 2026/09/25
Tai JunfeiHu DaijunHu ZhihengSaini AbhishekZuo PengChia Hou YiPeng GuochenYeong Wai YeeYan WentaoFan Zheng - Everolimus (EVE) is a key treatment for advanced clear cell renal cell carcinoma (ccRCC), mainly targeting AKT/mTOR signaling. However, developed resistance remains a major challenge for EVE treatment. Aberrant alternative splicing, particularly regulated by PTBP1, may represent a critical mechanism enabling the activation of these resistance-associated pathways. - Source: PubMed
Publication date: 2026/09/27
Pan Xiu-WuZheng Hong-FengLi Mu-ChenZhou Jia-LinZhang Hang-BiaoLyu Dong-HaoTang Yi-FanYang Tian-YueLiu Yi-FanLiu Zi-ChangMa Wen-JieZong Yuan-BoLiu Jian-GuiGong Zi-XuanZhang HaoDong Ke-QinZhou WangYe Jian-QinCui Xin-Gang - Stereotactic arrhythmia radioablation (STAR) is a promising noninvasive therapy for refractory ventricular tachycardia. Using scanned proton beams for STAR enables precisely focused, high doses of ionizing radiation. Effective mitigation of target motion is critical for safety but remains challenging due to the complex interplay between beam scanning and cardiorespiratory motion. We evaluated the safety and feasibility of accurately delivering gated scanned proton beams to a ventricular myocardial target and compared lesion outcomes of respiratory (single)- and cardiorespiratory (dual)-gated proton beams. - Source: PubMed
Publication date: 2026/09/27
Kang JagdipBijari Felicitas JChemli YanisChen Yen-LinDeng HelenDepauw NicolasDhaynaut MaevaGaronna AdrianoKim HyeongseokMacdonald-Soccorso MarinaMoon Sung-HyunNormandin Marc DWoodcock RebeccaMoshe Yaghoubian KFakhri Georges ElLevine RobertJee Kyung-WookImmo Lehmann H - Malignant cells under chemotherapy stress alter protein translation, necessitating sensitive methods to profile rare, surviving populations in vivo. We present a protocol for profiling low-input acute myeloid leukemia samples using an optimized ribosome profiling approach. We describe steps for lysing cell inputs, digesting unshielded RNA, enriching ribosome footprints, and gel-based size selection. We then detail procedures for constructing sequencing-ready libraries and using a computational pipeline to align and quantify both protected fragments and matching transcriptomes for reproducible translation analysis. For complete details on the use and execution of this protocol, please refer to Mayerhofer et al.. - Source: PubMed
Publication date: 2026/09/26
Mayerhofer ChristinaMayerhofer ErnstLi DanKristiansen TrineFeuchtinger TobiasScadden David T - The testicular functions of neuropeptide Y are largely unexplored in non-mammalian vertebrates as the few reports available remain restricted to fishes. Current research work reveals the testicular presence of npy and npyr in Hemidactylus flaviviridis and its variation in expression depending upon reproductive phases, marking the first documentation of such findings in reptilian species. Expression analysis of npy/npyr across different reproductive phases showed peak levels of both ligand and receptor during the recrudescent period, while the lowest expression occurred in regression. The investigation also examined the influence of NPY on markers of testicular spermatogenesis and steroidogenesis in H. flaviviridis. The in vitro exposure of wall lizard testes to NPY during recrudescent phase stimulated bcl 2, while simultaneously reduced caspase 3. NPY treatment also stimulated testicular expression of scf, c-kit, pcna, bmp-15 and gdf-9, along with gonadotropin receptor (fshr), and sex-steroid receptors (er-α, er-β, and ar). Further, NPY elevated star expression and promoted testosterone synthesis in wall lizard. Regarding the regulation of testicular npy and its receptor, npyr the expression of both ligand and its receptor was upregulated by the neuropeptide, kisspeptin, adipokines like leptin and nesfatin-1, and sex steroids such as DHT, and E, while they were suppressed by the gonadotropin, FSH and the neuropeptide, substance P. Overall, this investigation provides a detailed documentation of the presence, phase-specific pattern of expression, role, and hormonal regulation of NPY and its receptor in wall lizard testes. - Source: PubMed
Publication date: 2026/09/26
Chauhan VisheshRai UmeshTripathy MamtaKumar Sunil