PDSS1 抗体 (Middle Region)
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- 抗原 See all PDSS1 抗体
- PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
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抗原表位
- Middle Region
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适用
- 人, 小鼠, Cow, 犬, 豚鼠, 兔, 马, 大鼠
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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 PDSS1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- VIDDASSRRG KHTVNKIWGE KKAVLAGDLI LSAASIALAR IGNTTVISIL
- 预测反应
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%
- 产品特性
- This is a rabbit polyclonal antibody against PDSS1. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human PDSS1
- Top Product
- Discover our top product PDSS1 Primary Antibody
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anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) antibody
PDSS1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) (AA 1-183) antibodyPDSS1 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) (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
anti-Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) antibodyPDSS1 适用: 人, 小鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 415 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
- 别名
- PDSS1 (PDSS1 产品)
- 别名
- COQ1 antibody, COQ10D2 antibody, DPS antibody, RP13-16H11.3 antibody, SPS antibody, TPRT antibody, TPT antibody, TPT 1 antibody, hDPS1 antibody, 2610203G20Rik antibody, 2700031G06Rik antibody, Tprt antibody, mDLP1 antibody, mSPS1 antibody, tprt antibody, wu:fc11f12 antibody, wu:fd05d05 antibody, zgc:112058 antibody, T30F21.15 antibody, T30F21_15 antibody, solanesyl diphosphate synthase 1 antibody, decaprenyl diphosphate synthase subunit 1 antibody, prenyl (solanesyl) diphosphate synthase, subunit 1 antibody, prenyl (decaprenyl) diphosphate synthase, subunit 1 antibody, solanesyl diphosphate synthase 1 antibody, PDSS1 antibody, Pdss1 antibody, pdss1 antibody, SPS1 antibody
- 背景
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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.
Alias Symbols: COQ1, MGC70953, RP13-16H11.3, TPRT, TPT, hDPS1, DPS, SPS, TPT 1
Protein Interaction Partner: UBC,
Protein Size: 415 - 分子量
- 46 kDa
- 基因ID
- 23590
- NCBI登录号
- NM_014317, NP_055132
- UniProt
- Q5T2R2
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