SLC37A2 导读 基因简介 中英文全称:溶质载体家族37(甘油3 磷酸转运蛋白), 成员2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 OMIM/位置:11q24.2
Here, the authors identify Slc37a2 as a secretory lysosome sugar transporter that is required for maintenance of skeletal bone mass.doi:10.1038/s41467-023-36484-2P. NgAmy B. P. RibetQ. GuoBenjamin H MullinJ. W. TanE. Landao‐Bassonga...
Here, using organelle-resolution proteomics, we identify member a2 of the solute carrier 37 family (Slc37a2) as a SL sugar transporter. We demonstrate in mice that Slc37a2 localizes to the SL limiting membrane and that these organelles adopt a hitherto unnoticed but dynamic tubular network in...
基因名称: SLC37A2 基因又名: pp11662; SPX2 Gene ID: 219855 种属 Homo sapiens DNA序列编号: NM_198277.3 DNA描述 Homo sapiens solute carrier family 37 member 2 (SLC37A2), transcript variant 1, mRNA DNA大小: 4008 bp DNA编码区: atgcggtcctccctggctccgggagtctggttcttccgggccttctccagggacagctgg ...
英文名称:Rabbit Anti Human,Mouse,Rat SLC37A2 Antibody-Non-conjugated,中文名称:兔抗人、小鼠、大鼠SLC37A2抗体非结合,产品货号:CSB-PA021611GA01HU_50ul,[[长名称:兔抗人、鼠、大鼠SLC37A2,非结合型同义词名称:SLC37A2人、鼠、鼠抗体种反应性:人、
SLC37A2 deletion reprograms macrophages to a hyper-glycolytic process and accelerates LPS-induced inflammatory cytokine production, which partially depends on nicotinamide adenine dinucleotide (NAD+) biosynthesis. Blockade of glycolysis normalizes the differential expression of pro-inflammatory cytokines between...
SLC37A2 antibody 中文别名: SLC37A2兔多克隆抗体 CBNumber: CB35696418 分子式: 分子量: 0 MOL File: Mol file 化学性质安全信息用途供应商32 SLC37A2 antibody化学性质 安全信息 SLC37A2 antibody性质、用途与生产工艺 SLC37A2 antibody上下游产品信息 ...
SLC37A2 deletion reprograms macrophages to a hyper-glycolytic process and accelerates LPS-induced inflammatory cytokine production, which partially depends on nicotinamide adenine dinucleotide (NAD ) biosynthesis. Blockade of glycolysis normalizes the differential expression of pro-inflammatory cytokines between...
SLC37A4/G6PC3, but not SLC37A2, levels were induced in 3D CD133/SOX2-positive U87 neurospheres when compared to 2D monolayers. Silencing of SLC37A4/G6PC3 altered TGF-β-induced EMT biomarker SNAIL and cell chemotaxis. Conclusion: Two members of the G6Pase system, G6PC3 and SLC37A4...
SLC16A2基因变异会导致一种名叫“艾伦-赫恩登-达得利综合征(Allan-Herndon-Dudley syndrome)”的疾病,这个疾病是X连锁隐性遗传,临床就是以严重智力运动落后为主要表现;以肌张力低下、肌张力不全、锥体束征为主要的神经系统异常体征,这些特征与该患儿的临...