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- 抗原 See all AGXT 抗体
- AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This AGXT antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- 交叉反应
- 人
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein corresponding to Mouse AGXT
- Top Product
- Discover our top product AGXT Primary Antibody
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anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 96-125) antibody
AGXT 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB18848 unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 120-334) antibodyAGXT 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 112-294) antibodyAGXT 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 182-371) antibodyAGXT 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (Internal Region) antibodyVerified AGXT 适用: 人 ELISA, FACS, IF 宿主: 山羊 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 187-741) antibodyAGXT 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 183-392) antibodyAGXT 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 188-375) antibodyAGXT 适用: 人 WB 宿主: 小鼠 Monoclonal 1739CT804-82-83-1 unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) antibodyAGXT 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) antibodyAGXT 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB (M) 1:300-1:600, IHC/IF (H) 1:1000-1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS, pH 7.4, 0.02 % sodium azide
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
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- 抗原
- AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
- 别名
- AGXT (AGXT 产品)
- 背景
- AGXT (AGT) is a key enzyme in glyoxylate detoxification. Mutations of AGXT lead to primary hyperoxaluria type I, a rare metabolic disease which is characterized by deficient AGXT, excessive hepatic oxalate production that leads to renal failure.
- 分子量
- 46 kDa
- 基因ID
- 11611
- UniProt
- O35423
- 途径
- Monocarboxylic Acid Catabolic Process, Dicarboxylic Acid Transport
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