APOH Antibody (monoclonal) (M01)
- Known as:
- APOH Antibody (mab) (M01)
- Catalog number:
- AT1169a
- Product Quantity:
- 200 uL mg
- Category:
- -
- Supplier:
- Abgen
- Gene target:
- APOH Antibody (monoclonal) (M01)
Related genes to: APOH Antibody (monoclonal) (M01)
- Gene:
- APOH NIH gene
- Name:
- apolipoprotein H
- Previous symbol:
- B2G1
- Synonyms:
- BG
- Chromosome:
- 17q24.2
- Locus Type:
- gene with protein product
- Date approved:
- 1987-09-11
- Date modifiied:
- 2015-12-17
- Gene:
- GTF2H2B NIH gene
- Name:
- general transcription factor IIH subunit 2B (pseudogene)
- Previous symbol:
- -
- Synonyms:
- DKFZP686M0199
- Chromosome:
- 5q13.2
- Locus Type:
- pseudogene
- Date approved:
- 2008-07-04
- Date modifiied:
- 2015-11-09
- Gene:
- POLR1A NIH gene
- Name:
- RNA polymerase I subunit A
- Previous symbol:
- -
- Synonyms:
- DKFZP586M0122, FLJ21915, RPO1-4, RPA1
- Chromosome:
- 2p11.2
- Locus Type:
- gene with protein product
- Date approved:
- 2003-04-01
- Date modifiied:
- 2017-06-28
- Gene:
- TDRP NIH gene
- Name:
- testis development related protein
- Previous symbol:
- C8orf42
- Synonyms:
- INM01, TDRP1, TDRP2
- Chromosome:
- 8p23.3
- Locus Type:
- gene with protein product
- Date approved:
- 2005-07-28
- Date modifiied:
- 2015-08-26
Related products to: APOH Antibody (monoclonal) (M01)
Related articles to: APOH Antibody (monoclonal) (M01)
- Acute liver failure (ALF) is a serious clinical disease. Immune infiltration and oxidative stress (OS) play an important role in ALF, but the combination of oxidative stress and immune infiltration in ALF has not been explored. - Source: PubMed
Publication date: 2026/09/09
Dai LuTan JungangZhou ZhiminChen ChengcongHu GuoxinGuo Ling - Anti-β2-glycoprotein I (anti-β2GPI) antibodies are central to antiphospholipid syndrome. The APOH locus has been associated with anti-β2GPI, but the causal variant and thrombotic risk implications remain unclear. - Source: PubMed
Publication date: 2026/09/07
Lalaurie ChristopheLiu LiliKhan AtlasWang ChenRich Stephen SBarr R GrahamBernstein Elana JKiryluk KrzysztofMcDonnell ThomasLuo Yiming - Lipoproteins are molecules composed of phospholipids and apolipoproteins that transport triacylglycerol and cholesterol in blood and are implicated in the development of many diseases. - Source: PubMed
Publication date: 2026/07/14
Łukaszuk BartłomiejChabowski AdrianZiemba AndrzejChoromańska BarbaraMyśliwiec PiotrSupruniuk KatarzynaMikłosz Agnieszka - Chronic kidney disease (CKD) is a major health burden, yet its underlying mechanisms and early predictors remain poorly understood. - Source: PubMed
Publication date: 2026/07/09
Ru DongmeiWang XinyueXiao CongmeiCheng ManjingZhou FuxianMamuti ReziwanguliXi YueDeng KuiWang JiaoXu LinZheng Ju-ShengChen Yu-Ming - Cetaceans face the risk of thromboembolism due to diving and decompression responses. However, cetaceans maintain normal blood circulation. This study explores the molecular mechanisms cetaceans use to mitigate diving-associated hemostatic challenges during diving. Forty-six species were analyzed, including 18 cetaceans, 9 artiodactyls, and 19 other terrestrial mammals. Thirty-nine anticoagulant genes and proteins were examined, identifying 6 genes (ANXA2, ANXA5, FGA, FGB, PLAUR, and PLG) with conserved evolution, 4 genes (ANXA2, PDGFB, SH2B3, THBS1) with positive selection, and 12 proteins (APOH, FGA, FGB, FGG, GP1BA, PLAU, PRKCD, PRKG1, SERPINF2, SERPING1, TMPRSS6, and TMX1) with specific amino acid sites in cetaceans. Ancestral state reconstruction revealed independent evolution of deep diving behavior in different cetacean lineages, particularly within Odontoceti. Correlation analysis linked the evolution of the APOE gene with diving depth, suggesting its role in diving adaptation. These analyses suggest that cetaceans may help reduce the risk of thrombosis during diving by lowering platelet activity, enhancing fibrinolysis, and modulating the coagulation cascade. These analyses suggest that cetaceans may mitigate diving-associated thrombotic risk by modulating platelet activity, fibrinolysis, and the coagulation cascade. Overall, this study identifies candidate anticoagulant-related genes and amino acid substitutions for future functional validation of hemostatic adaptation in cetaceans. - Source: PubMed
Publication date: 2026/07/06
Lv WenjunCao LiZhang YaXu ShixiaRen Wenhua