GPD1L 抗体 (AA 1-351)
-
- 抗原 See all GPD1L 抗体
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
-
抗原表位
- AA 1-351
-
适用
- 人
-
宿主
- 小鼠
-
克隆类型
- 单克隆
-
标记
- This GPD1L antibody is un-conjugated
-
应用范围
- Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF)
- 免疫原
- Recombinant human GPD1L (1-351aa) purified from E. coli
- 克隆位点
- AT14E2
- 亚型
- IgG1 kappa
- Top Product
- Discover our top product GPD1L Primary Antibody
-
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (AA 44-73), (N-Term) antibody
GPD1L 适用: 人, 小鼠 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB28552 unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (AA 47-77), (N-Term) antibodyGPD1L 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) antibodyGPD1L 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (AA 1-351) antibodyGPD1L 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (AA 1-351) antibodyGPD1L 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (C-Term) antibodyGPD1L 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 小鸡, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) (AA 1-351) antibodyGPD1L 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 mg/mL
- 储存条件
- 4 °C,-20 °C,-80 °C
- 储存方法
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
-
- 抗原
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
- 别名
- GPD1L (GPD1L 产品)
- 背景
- GPD1L is converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). GPD1L is thought to affect trafficking of the cardiac sodium current to the cell surface. Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia.
- NCBI登录号
- NP_055956
-
