GPD1L 抗体 (N-Term)
Quick Overview for GPD1L 抗体 (N-Term) (ABIN952587)
抗原
See all GPD1L 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 47-77, N-Term
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特异性
- This antibody reacts to GPD1L.
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交叉反应 （详细）
- Species reactivity (tested):Human and Mouse.
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纯化方法
- Affinity chromatography on Protein A
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免疫原
- KLH conjugated synthetic peptide between 47-77 amino acids from the N-terminal region of human GPD1L
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亚型
- Ig Fraction
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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) 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, ELISA, ICC, IF 宿主: 小鼠 Monoclonal AT14E2 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) (AA 1-351) antibodyGPD1L 适用: 人 WB, IP 宿主: 兔 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
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS, 0.09 % (W/V) sodium azide
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
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别名
- GPD1L
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背景
- The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).Synonyms: GPD1-L, Glycerol-3-phosphate dehydrogenase 1-like protein, KIAA0089
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分子量
- 38419 Da
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基因ID
- 23171
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NCBI登录号
- NP_055956
抗原
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