用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Positive WB detected in | Human peripheral blood platelets |
| Positive IHC detected in | human spleen tissue, human liver tissue, human heart tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
推荐稀释说明
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. Sample-dependent, Check data in validation data gallery.
详细信息
背景信息
Function CD36, also known as platelet glycoprotein 4, is an integral membrane glycoprotein that acts as a scavenger receptor. CD36 can bind to multiple ligands, including thrombospondin-1, collagen, oxidized phospholipids, oxidized low-density lipoprotein, and long-chain fatty acids. CD36 can also bind to erythrocytes parasitized by Plasmodium falciparum and apoptotic cells. CD36 mediates different biological processes, acting as a signaling hub in angiogenesis, inflammatory response, and fatty acid metabolism. Tissue specificity CD36 is present on the surface of various cells types, such as adipocytes, monocytes, macrophages, platelets, microvascular endothelial cells, dendritic cells, and hematopoietic precursors of red cells. Involvement in disease Mutations in CD36 can give rise to platelet glycoprotein IV deficiency, a type of macrothrombocytopenia. Polymorphisms in CD36 can increase susceptibility to malaria. AAGIC haplotype at the CD36 locus increases the risk of coronary heart disease. Disruption of CD36-dependent pathways and certain SNPs in the CD36 gene are attributed to impaired fatty acid metabolism, glucose intolerance, Alzheimer's disease, atherosclerosis, arterial hypertension, diabetes, and cardiomyopathy. Isoforms Apart from the full-length protein (isoform 1), one additional shorter isoform has been reported (PMID: 7509795). Other alternative isoforms have also been detected on the mRNA level (PMID: 17673938). Post-translational modifications The extracellular domain of CD36 is extensively glycosylated. Glycosylation is needed for the transport of CD36 to the plasma membrane, as well as mediating recognition and binding to ligands. Cytoplasmic tails of transmembrane domains can be phosphorylated and play a role in signal transduction. Intracellular domains can be additionally acetylated, ubiquitinated, and palmitoylated (PMID: 28919632). Cellular localization CD36 is present on the cell surface.
文献引用 (75)
Early-life exercise extends healthspan but not lifespan in mice.
早期运动可以延长小鼠的健康寿命,但不能延长其寿命
Engineered Spirulina platensis for treating rheumatoid arthritis and restoring bone homeostasis.
工程化螺旋藻用于治疗类风湿性关节炎和恢复骨骼稳态
S100P is a ferroptosis suppressor to facilitate hepatocellular carcinoma development by rewiring lipid metabolism
S100P 是一种铁死亡抑制剂,通过重新连接脂质代谢来促进肝细胞癌的发展
Pyruvate Carboxylase in Macrophages Aggravates Atherosclerosis by Regulating Metabolism Reprogramming to Promote Inflammatory Responses Through the Hypoxia-Inducible Factor-1 Signaling Pathway.
巨噬细胞中的丙酮酸羧化酶通过调节代谢重编程,经由缺氧诱导因子-1信号通路促进炎症反应,从而加剧动脉粥样硬化
Conjugated Lithocholic Acid Activates Hepatic TGR5 to Promote Lipotoxicity and MASLD-MASH Transition by Disrupting Carnitine Biosynthesis.
共轭石胆酸激活肝脏TGR5,通过破坏肉碱生物合成促进脂毒性和MASLD-MASH转变
IGF2BP3/ESM1/KLF10/BECN1 positive feedback loop: a novel therapeutic target in ovarian cancer via lipid metabolism reprogramming.
IGF2BP3/ESM1/KLF10/BECN1 正反馈环路:通过脂质代谢重编程治疗卵巢癌的新靶点
Remdesivir inhibits endothelial activation and atherosclerosis by coupling TAL1 to TRAF6.
瑞德西韦通过将 TAL1 与 TRAF6 连接起来抑制内皮细胞活化和动脉粥样硬化
Porcine jejunal-derived extracellular vesicles participate in the regulation of lipid metabolism.
猪空肠来源的细胞外囊泡参与脂质代谢的调节
Macrophage EP4 Deficiency Drives Atherosclerosis Progression via CD36-Mediated Lipid Uptake and M1 Polarization
巨噬细胞EP4缺陷通过CD36介导的脂质摄取和M1极化驱动动脉粥样硬化进展
HKDC1 promotes ovarian cancer progression through boosting lipid metabolism and immune escape by stabilizing G6PC/G6PC2.
HKDC1 通过稳定 G6PC/G6PC2 来促进脂质代谢和免疫逃逸,从而促进卵巢癌的进展
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