GPD1L 抗体 (AA 19-351) (APC)
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北京 101111
Quick Overview for GPD1L 抗体 (AA 19-351) (APC) (ABIN7994521)
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 19-351
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原理
- Anti-GPD1L Antibody APC Conjugated
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特异性
- No cross reactivity with other proteins.
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human GPD1L recombinant protein (Position: A19-T351).
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亚型
- IgG
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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 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) (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 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) (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
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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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
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Background: GPD1L is a human gene. It is mapped to 3p22.3. The protein encoded by this gene contains a glycerol-3-phosphate dehydrogenase (NAD+) motif and shares 72 % sequence identity with GPD1. 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).
Gene Full Name: glycerol-3-phosphate dehydrogenase 1 like
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基因ID
- 23171
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UniProt
- Q8N335
抗原
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