MVK 抗体
Quick Overview for MVK 抗体 (ABIN7237444)
抗原
See all MVK 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant protein of human MVK
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亚型
- IgG
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anti-Mevalonate Kinase (MVK) (AA 297-396) antibody
MVK 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 2C5 unconjugated
anti-Mevalonate Kinase (MVK) (AA 297-396) antibodyMVK 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (Internal Region) antibodyMVK 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (AA 1-396) antibodyMVK 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) antibodyMVK 适用: 人, 猴 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (Internal Region) antibodyMVK 适用: 人 WB, IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (AA 179-228) antibodyMVK 适用: 人, 小鼠, 猴, Cow, 犬, 兔, Pig, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (AA 107-156) antibodyMVK 适用: 人, 小鼠, 大鼠, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (Internal Region) antibodyMVK 适用: 人, 猴 WB, IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Mevalonate Kinase (MVK) (AA 1-396) antibodyMVK 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB 1:200-1:1000, IHC 1:100-1:300
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.4 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- MVK (Mevalonate Kinase (MVK))
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别名
- MVK
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背景
- This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash.
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分子量
- 42 kDa
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UniProt
- Q03426
抗原
-
