BMP2 ELISA kit
- Known as:
- BMP2 Enzyme-linked immunosorbent assay test reagent
- Catalog number:
- DL-BMP2-CH
- Product Quantity:
- 96T
- Category:
- Elisa Kits
- Supplier:
- WDSTD
- Gene target:
- BMP2 ELISA kit
Related genes to: BMP2 ELISA kit
- Gene:
- BMP2 NIH gene
- Name:
- bone morphogenetic protein 2
- Previous symbol:
- BMP2A
- Synonyms:
- -
- Chromosome:
- 20p12.3
- Locus Type:
- gene with protein product
- Date approved:
- 1990-06-11
- Date modifiied:
- 2016-10-05
- Gene:
- BMP4 NIH gene
- Name:
- bone morphogenetic protein 4
- Previous symbol:
- BMP2B
- Synonyms:
- -
- Chromosome:
- 14q22.2
- Locus Type:
- gene with protein product
- Date approved:
- 1990-06-11
- Date modifiied:
- 2016-10-05
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- To map and categorize the existing literature on the use of bone morphogenetic proteins (BMPs) in dentinogenesis and pulp tissue regeneration, identifying research trends, experimental approaches, and knowledge gaps to inform future studies and potential clinical translation. - Source: PubMed
Publication date: 2026/05/18
Portes-Zeno Ana PaulaDos Santos Alexandre GuimarãesSipert Carla RenataFonseca-Gonçalves AndréaRisso Patrícia AndradeMaia Lucianne Cople - Laryngotracheal fibrosis is a rare but severe complication of prolonged intubation, leading to airway narrowing, respiratory distress, dysphonia, and, in advanced cases, life-threatening airway obstruction. Current treatments are primarily surgical, while pharmacologic approaches such as mitomycin C, corticosteroids, or 5-fluorouracil show inconsistent efficacy and potential toxicity. Thus, there remains a critical need for safe and effective antifibrotic therapies. Transforming growth factor-beta (TGF-β) is a key mediator of fibrosis, promoting fibroblast activation, migration, and expression of profibrotic markers such as alpha-smooth muscle actin (α-SMA). - Source: PubMed
Publication date: 2026/05/09
Toth EnikoSzabo KittiVegh Attila GergelyZvara AgnesPuskas Laszlo GBach AdamMigh EdeHorvath PeterTiszlavicz LaszloRovo LaszloKeller-Pinter Aniko - Chronic rhinosinusitis (CRS) comprises distinct phenotypes with divergent inflammatory and tissue remodeling patterns. Bone morphogenetic proteins (BMPs) are key regulators of airway repair; however, it remains unclear whether phenotypic differences between CRS with nasal polyps (CRSwNP) and without nasal polyps (CRSsNP) are associated with BMP ligand abundance or downstream pathway activity. We investigated phenotype-specific BMP/Smad pathway patterns and their potential relevance to airway remodeling. - Source: PubMed
Publication date: 2026/04/22
Eyibilen AhmetHira Serdar - The early gonads of mammals contain primordial germ cells (PGCs) and gonadal somatic cells. In females, the gonadal somatic cells promote the specification of PGCs into oogonia and their entry into meiosis, which is crucial for oogenesis. Although single-cell transcriptome sequencing technology holds significant advantages in cell type identification, its inability to resolve spatial positional information substantially hampers research on communication mechanisms between germ cells and adjacent somatic cells. Here, we utilized high-resolution spatial transcriptomic technology to dissect the spatial dynamics of various cell types during the specification of PGCs into oogonia and their entry into meiosis in porcine gonads. We clarified the spatial localization of two waves of granulosa cells in the supporting cell lineage and their roles in regulating germ cell development. Furthermore, we found that interstitial and endothelial cells were predominantly located in the medullary region of the early gonads. Notably, cell-cell communication analysis revealed the critical role of BMP signaling (BMP2, BMP4 and GDF5) in driving the specification of PGCs into oogonia and their subsequent entry into meiosis. Our study provides a spatially resolved understanding of the PGC-to-oogonia specification in vivo and offers critical resources for reconstituting oogenesis in vitro. - Source: PubMed
Publication date: 2026/03/30
He PengchengXia WenzheChen TianzhiYan YaxuanGao DengfengTeng YadiZhao TingChen XinzeFeng ZhiqiangLi RunboWang MengKe YuwenHan Jianyong - Osteokines, primarily secreted by bone, have been implicated in brain function and Parkinson's disease (PD) pathogenesis, yet their circulating levels in PD and potential role in the relationship between bone mineral density (BMD) and PD remain unclear. 80 participants (40 PD patients and 40 controls) were enrolled to measure plasma levels of eight osteokines (GPNMB, OPN, SOST, DKK1, RANKL, FGF23, BMP2, and BMP4) and assess their associations with clinical scales. Mendelian randomization (MR), SMR, and colocalization analyses were performed to evaluate causal relationships between osteokines and PD. Restricted cubic spline (RCS) models were applied to explore nonlinear associations between BMD, osteokines, and PD. GPNMB levels were significantly elevated in PD patients and showed a linear association with PD risk. Higher GPNMB levels were associated with worse cognitive performance and clinical severity, while higher SOST levels correlated with milder symptoms. Genetic analyses consistently supported a causal and colocalized relationship between GPNMB and PD. Total coxa BMD and T-score were lower in PD, but not statistically significant. RCS analysis revealed an "n-shaped" association between total coxa T-score and both PD and GPNMB levels. Overall, GPNMB appears causally linked to PD risk and may mediate the bone-brain axis connecting BMD with PD susceptibility. - Source: PubMed
Publication date: 2026/03/18
Guo XingzhiWei PeiyaoShi WenzhiZhou RongLi Rui