OAT 抗体 (AA 25-75)
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北京 101111
Quick Overview for OAT 抗体 (AA 25-75) (ABIN7450521)
抗原
See all OAT 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 25-75
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原理
- Rabbit anti-OAT Antibody, Affinity Purified
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纯化方法
- Affinity Purified
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免疫原
- Between AA 25 and 75
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亚型
- IgG
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anti-Ornithine Aminotransferase (OAT) (AA 1-301) antibody
OAT 适用: 人 WB, IHC, ICC, IP 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) (AA 160-439) antibodyOAT 适用: 人 WB, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) (Middle Region) antibodyOAT 适用: 人, 小鼠, 大鼠, Cow, 马, 兔, 犬, 豚鼠, 斑马鱼, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) antibodyOAT 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) (AA 27-55), (N-Term) antibodyOAT 适用: 人, 小鼠, 大鼠 WB, IF, FACS, IHC (p) 宿主: 兔 Polyclonal RB21924 unconjugated
anti-Ornithine Aminotransferase (OAT) antibodyOAT 适用: 人 IHC, IHC (p) 宿主: 小鼠 Monoclonal AT23A2 unconjugated
anti-Ornithine Aminotransferase (OAT) (C-Term) antibodyOAT 适用: 人, 小鼠, 大鼠, Cow, 马, 兔, 犬, 豚鼠, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) (Internal Region) antibodyOAT 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Ornithine Aminotransferase (OAT) (AA 33-439) antibodyOAT 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal AT23A2 unconjugated
anti-Ornithine Aminotransferase (OAT) antibodyOAT 适用: 人, 小鼠, 大鼠 WB, IHC, FACS, IF/ICC 宿主: 兔 Polyclonal unconjugated
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应用备注
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IP: 2 - 10 μg/mg lysate
WB: 1:2,000 - 1:10,000
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限制
- 仅限研究用
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浓度
- 1000 μg/mL
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缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
- 4 °C
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有效期
- 12 months
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- OAT (Ornithine Aminotransferase (OAT))
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别名
- OAT
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背景
- Background: Ornithine aminotransferase (OAT) is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy [taken from NCBI Entrez Gene (Gene ID: 4942)].
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基因ID
- 4942
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UniProt
- P04181
抗原
-
