Gast (Rat) ELISA Kit
- Known as:
- Gast (Rat) Enzyme-linked immunosorbent assay test Kit
- Catalog number:
- KA0319
- Product Quantity:
- 1 Kit
- Category:
- Peptides
- Supplier:
- Abno
- Gene target:
- Gast (Rat) ELISA Kit
Related genes to: Gast (Rat) ELISA Kit
- Gene:
- GAST NIH gene
- Name:
- gastrin
- Previous symbol:
- GAS
- Synonyms:
- -
- Chromosome:
- 17q21.2
- Locus Type:
- gene with protein product
- Date approved:
- 2001-06-22
- Date modifiied:
- 2015-08-25
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- Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) is a UVA filter widely used in cosmetic formulations. The present study evaluated the toxicological profile and conducted a human health risk assessment of DHHB based on available toxicological and exposure data. Overall, the available studies indicate low acute toxicity, no evidence of genotoxicity, and minimal skin irritation or sensitization potential. For risk characterization, the maternal no-observed-adverse-effect level (NOAEL) of 200 mg/kg bw/day derived from a reproductive and developmental toxicity study in rats was selected as the point of departure because it represents the most relevant endpoint for systemic exposure. Human exposure was estimated using the cosmetic exposure assessment approach recommended by the Ministry of Food and Drug Safety (MFDS). The systemic exposure dose (SED) was calculated assuming daily use of sunscreen products (17 g/day), a maximum DHHB concentration of 10%, and a dermal absorption rate of 0.15%. Based on these parameters, the SED was estimated to be 0.0425 mg/kg bw/day. Comparison of the SED with the selected NOAEL yielded a margin of safety (MoS) of 4,705, which exceeds the safety threshold of 100 typically applied in cosmetic risk assessments. These results indicate that DHHB presents a low risk to human health when used as a UV filter in cosmetic products at concentrations up to 10%. - Source: PubMed
Publication date: 2026/05/16
Lee Jung DaeKim Hyang YeonLee Joo YoungSung Chi RimKwack Seung JunYoon TaehyungKim Kyu-Bong - Matrix stiffness increases during fibrosis and drives hepatic stellate cell (HSC) activation through YAP-dependent mechanotransduction. Although recent studies have revealed HSC heterogeneity beyond classical quiescent and fully activated states, how physiological-range stiffness influences activation trajectories underlying this heterogeneity remains unclear. This study aimed to determine how substrate stiffness shapes the transcriptomic profiles and biases activation trajectories. - Source: PubMed
Publication date: 2026/09/01
Inada KentoMiyoshi MasatoKakinuma SeiWatakabe KeiyaMochida TomohiroShimizu TaroTsuchiya JunNobusawa TsubasaKaneko ShunKawai-Kitahata FukikoMurakawa MiyakoNitta SayuriNakagawa MinaAsahina YasuhiroOkamoto Ryuichi - While most sodium (Na) MRI studies focus on apparent tissue sodium concentration (aTSC), longitudinal (T₁) and transverse (T₂*) relaxation times may provide additional microstructural and physiological information. This study aimed to establish reference values for Na T₁ and bi-exponential T₂* in human lower-leg muscle at 3 T and 7 T, evaluate methodological factors influencing T₂* quantification, and assess the reproducibility of aTSC. - Source: PubMed
Publication date: 2026/08/21
Zeitouni NourRuck LaurentGast Lena VUder MichaelDörfler ArndNagel Armin MGerhalter Teresa - Impact of prior inactivated poliovirus vaccine (IPV) doses on nasal and pharyngeal viral replication following subsequent poliovirus exposure remains unclear. Circulating vaccine-derived poliovirus detection in IPV-only countries necessitates better understanding of IPV's role in inducing nasal and pharyngeal mucosal immunity. - Source: PubMed
Publication date: 2026/08/18
Zaman KhalequBandyopadhyay Ananda SGast ChrisGoswami Doli RHoque MasumaRaqib RubhanaHossain LokmanHaque WardaIslam ArifaRashid Harun-Or-Rahman MustafizurAguirre GabrielaBrickley Elizabeth BGodin AudreyWeiner Joshua ABurke Rachel MAckerman Margaret ESifontes GiovannaMainou Bernardo AWright Peter FRüttimann Ricardo - Following bereavement, a minority experiences severe, persistent, and disabling grief, termed prolonged grief disorder (PGD). Establishing individual differences in how grief develops over time can guide clinical decision-making, yet has only recently received empirical scrutiny. The present review synthesizes results from grief trajectory studies. - Source: PubMed
Publication date: 2026/08/16
Eisma Maarten Cvan Rhee LiseGast Julia ALenferink Lonneke I M