Polyclonal ABHD12B antibody
- Known as:
- Polyclonal ABHD12B (anti-)
- Catalog number:
- stj91421
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- St Johns Labs
- Gene target:
- Polyclonal ABHD12B antibody
Related genes to: Polyclonal ABHD12B antibody
- Gene:
- ABHD12B NIH gene
- Name:
- abhydrolase domain containing 12B
- Previous symbol:
- C14orf29
- Synonyms:
- BEM46L3
- Chromosome:
- 14q22.1
- Locus Type:
- gene with protein product
- Date approved:
- 2002-11-27
- Date modifiied:
- 2018-05-03
Related products to: Polyclonal ABHD12B antibody
Related articles to: Polyclonal ABHD12B antibody
- Lung adenocarcinoma cells exhibit a marked propensity for brain metastasis, in which they face unique metabolic challenges imposed by the microenvironment. The mechanisms that enable lung adenocarcinoma cells to adapt to these constraints represent potential therapeutic targets. In this study, we identified the neuropeptide VGF as a clinically relevant driver of brain metastatic progression. VGF expression was markedly upregulated in lung adenocarcinoma brain metastases, and elevated VGF expression was associated with an increased risk of brain metastasis and poor survival outcomes. Moreover, brain-derived signals induced VGF expression in lung adenocarcinoma cells, promoting cell survival and proliferation through enhanced mitochondrial oxidative phosphorylation and ATP production. Mechanistically, the N-terminal domain of VGF-a nonclassically secreted peptide-interacted with the hydrolase domain of ABHD12B to suppress cardiolipin degradation, leading to increased cardiolipin levels, stabilization of mitochondrial membranes, and a shift toward mitochondrial fusion over excessive fission. These changes helped meet the heightened energetic demands of metastatic cells in the brain. Genetic deletion of the VGF N-terminal domain disrupted mitochondrial fusion, impaired oxidative metabolism, and significantly reduced brain colonization in mouse models of brain metastasis. Together, these findings uncover a role for VGF and establish the VGF-ABHD12B-cardiolipin axis as a critical mechanism underlying metabolic adaptation in lung adenocarcinoma brain metastases, highlighting the potential of this pathway as a therapeutic target for intervention. - Source: PubMed
Wang YibeiSheng XinyueYang YiLiu ChenWang ShubaoGuo RuixiGu YueChen MingZhang HongyanDu JingjingQin XiaoxueMiao ZiweiWu PengfeiQu XiujuanLi Bo - The effects of low-sodium salt mixture substitution on the sensory quality, protein oxidation, and hydrolysis of air-dried chicken and its molecular mechanisms were investigated based on tandem mass tagging (TMT) quantitative proteomics. The composite salt formulated with 1.6% KCl, 0.8% MgCl, and 5.6% NaCl was found to improve the freshness and texture quality scores. Low-sodium salt mixture substitution significantly decreased the carbonyl content (1.52 nmol/mg), surface hydrophobicity (102.58 μg), and dimeric tyrosine content (2.69 A.U.), and significantly increased the sulfhydryl content (74.46 nmol/mg) and tryptophan fluorescence intensity, suggesting that protein oxidation was inhibited. Furthermore, low-sodium salt mixture substitution significantly increased the protein hydrolysis index (0.067), and cathepsin B and L activities (102.13 U/g and 349.25 U/g), suggesting that protein hydrolysis was facilitated. The correlation results showed that changes in the degree of protein hydrolysis and protein oxidation were closely related to sensory quality. TMT quantitative proteomics indicated that the degradation of myosin and titin as well as changes in the activities of the enzymes, CNDP2, DPP7, ABHD12B, FADH2A, and AASS, were responsible for the changes in the taste quality. In addition, CNDP2, ALDH1A1, and NMNAT1 are key enzymes that reduce protein oxidation. Overall, KCl and MgCl composite salt substitution is an effective method for producing low-sodium air-dried chicken. - Source: PubMed
Publication date: 2024/02/28
Li JianhaoShi ZihangFan XiankangDu LihuiXia QiangZhou ChangyuSun YangyingXu BaocaiPan Daodong - Asthma is characterized by airway hyperresponsiveness, reversible airway obstruction, and chronic airway inflammation. It is the most common chronic disease in childhood. However, the diagnosis of childhood asthma remains challenging, and there is an urgent need to develop new diagnostic methods. - Source: PubMed
Publication date: 2024/01/24
Ding HuiShi ZhaolingLin HaiboSun YuanZhang LuLiu FeiyanWang XuelinZhang ZhihongZhang Guocheng - Genome-wide association studies showed the relationship of , , , , and with chronic periodontitis. The study's objective was to investigate different molecular patterns and evolutionary forces acting on the mentioned genes. The investigation of molecular patterns encompasses the study of compositional parameters, expression profile, physical properties of genes, codon preferences, degree of codon bias, determination of the most influential codons, and assessment of actions of evolutionary forces, such as mutations and natural selection. The overall compositional analysis revealed the dominance of A and G nucleotides compared to T and C. A relatively low codon usage bias is observed. The CTG codon is the most overused codon, followed by TCC. The genes, and , preferred GC-ending codons, while , , and preferred AT-ending codons. The presence of directional mutational force and natural selection was found to operate codon usage in genes envisaged, and selective forces were dominant over mutational forces. Apart from mutation and selection forces, compositional constraints also played imperative roles. The study enriched our knowledge of specific molecular patterns associated with the set of genes significantly associated with chronic periodontitis. Further studies are warranted to identify more genetic signatures associated with the disease. - Source: PubMed
Publication date: 2022/10/24
Khandia RekhaPandey MeghaRzhepakovsky Igor VladimirovichKhan Azmat AliLegaz Isabel - We sought to replicate findings from published genome-wide association studies (GWAS), linking specific candidate gene loci with periodontitis-related clinical/microbial traits. - Source: PubMed
Publication date: 2022/03/16
Yang TeresaCheng BinNoble James MReitz ChristianePapapanou Panos N