ATP1A2 基因简介 中英文全称:ATP 酶, Na+/K+转运, α2(+)肽 ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide 分布:钠: 钾交换ATP 酶复 合体|膜|融入膜 活性:核苷酸结合|镁离子结合|钠: 钾交换 ATP 酶|ATP 结合|一价无机阳离子转运蛋白|ATP 酶, 偶联 跨膜运输离子, 磷酸化机制|水解酶|水...
ATP1A2基因检测检测的是人的基因序列变化及表征数据库中标号为477的核酸分子上的碱基序列。它的突序及序列异常会引起正在通过基因解码技术进行收集、查证并编辑,请关注佳学基因,获得及时更新的人类基因序列变化与疾病表征数据库的更新内容。针对基因信息变化所产生的健康问题的靶向药物情况正在通过基因解码技术进行收集、查...
别名: AT1A2_HUMAN; Atp1a2; FHM2; KIAA0778; MHP2; Na(+)/K(+) ATPase alpha-2 subunit; Na+/K+ ATPase alpha 2 subunit; Sodium potassium ATPase; Sodium pump subunit alpha 2; Sodium pump subunit alpha-2; Sodium/potassium transporting ATPase alpha 2 chain; Sodium/potassium transporting ATPa...
诊断检测提示ATP1A2(c.2285G> C;p.Gly762Ala)有可疑的致病性突变,该基因和广泛的表型谱相关,涵盖家族性偏瘫型偏头痛2型(FHM2)和儿童交替性偏瘫。先前的病例系列表明,FMH2发作可能会延长,使人虚弱并与意识障碍和发热相关。皮质水肿已有描述...
ATP1A2 Polyclonal antibody ATP1A2 Polyclonal Antibody for WB, IHC, IF/ICC, FC (Intra), ELISA Cat No. 16836-1-AP Publications(22) Host / Isotype Rabbit / IgG Reactivity human, mouse, rat and More (2) Applications WB, IHC, IF/ICC, FC (Intra), ELISA and More (1) Synonyms ...
产品名称 人有机阴离子转运多肽1A2OATP1A2 elisa试剂盒 产品规格 48T 96T 有效成分含量 99 检测方法 酶联免疫 样本 血清,血浆,尿液,组织,细胞上 保质期 6个月 标记物 检测抗体-HRP 储存条件 2-8℃,避光防潮保存 用途范围 仅供研究使用,不得用于临床实验 是否进口 否 包装规格 48T 灵敏度 最...
Cat No.55179-1-AP 浓度:350 μg/ml 库存:现货 点击咨询售前客服 点击咨询售后客服 实验方案 Product Specific Protocols WB protocol for ATP1A2-Specific antibody 55179-1-APDownload protocol IHC protocol for ATP1A2-Specific antibody 55179-1-APDownload protocol ...
68505-2-PBS targets ATP1A2 as part of a matched antibody pair: MP50523-1: 68505-2-PBS capture and 68504-2-PBS detection (validated in Cytometric bead array) MP50523-2: 68505-2-PBS capture and 68504-1-PBS detection (validated in Cytometric bead array) Unconjugated mouse monoclonal antibody...
68504-1-PBS targets ATP1A2 as part of a matched antibody pair: MP50523-2: 68505-2-PBS capture and 68504-1-PBS detection (validated in Cytometric bead array) Unconjugated mouse monoclonal antibody pair in PBS only (BSA and azide free) storage buffer at a concentration of 1 mg/mL, ready...
ATP1A2 mutations are loss-of-function mutations that are thought to result in slower glial reuptake of glutamate and thus hyperexcitability. From: Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease (Fifth Edition), 2015 ...