PDSS1 抗体
Quick Overview for PDSS1 抗体 (ABIN2458992)
抗原
See all PDSS1 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Antibody is purified by peptide affinity chromatography method.
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免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PDSS1.
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anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) (AA 1-183) antibody
PDSS1 适用: Mycobacterium smegmatis ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) (AA 241-290) antibodyPDSS1 适用: 人, 小鼠, Cow, 犬, 豚鼠, 兔, 马, 大鼠, Pig, Bat, 小鸡, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) (AA 182-231) antibodyPDSS1 适用: 人, 小鼠, Cow, 犬, 豚鼠, 兔, Pig, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) antibodyPDSS1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) (Middle Region) antibodyPDSS1 适用: 人, 小鼠, Cow, 犬, 豚鼠, 兔, 马, 大鼠, Pig, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- PDSS1 antibody can be used for detection of PDSS1 by ELISA at 1:12500. PDSS1 antibody can be used for detection of PDSS1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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浓度
- 1 mg/mL
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缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
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储存条件
- 4 °C/-20 °C
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储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store PDSS1 antibody at -20 °C.
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- PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
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别名
- PDSS1
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背景
- PDSS1 is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. PDSS1 catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in PDSS1 gene are a cause of coenzyme Q10 deficiency.The protein encoded by this gene is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in this gene are a cause of coenzyme Q10 deficiency.
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分子量
- 46 kDa
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基因ID
- 23590
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NCBI登录号
- NP_055132
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UniProt
- Q5T2R2
抗原
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