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PDSS2 抗体

PDSS2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7243715
发货至: 中国
  • 抗原 See all PDSS2 抗体
    PDSS2 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 2 (PDSS2))
    适用
    • 28
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    宿主
    • 39
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    克隆类型
    • 41
    • 2
    多克隆
    标记
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    This PDSS2 antibody is un-conjugated
    应用范围
    • 14
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    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human PDSS2
    亚型
    IgG
    Top Product
    Discover our top product PDSS2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:25-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.3 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    PDSS2 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 2 (PDSS2))
    别名
    PDSS2 (PDSS2 产品)
    别名
    dlp1 antibody, C6orf210 antibody, COQ10D3 antibody, DLP1 antibody, bA59I9.3 antibody, hDLP1 antibody, zgc:92156 antibody, 5430420P03Rik antibody, Gm60 antibody, Plmp antibody, kd antibody, mDLP1 antibody, decaprenyl diphosphate synthase subunit 2 antibody, prenyl (decaprenyl) diphosphate synthase, subunit 2 antibody, decaprenyl-diphosphate synthase subunit 2 antibody, decaprenyl diphosphate synthase subunit 2 Dlp1 antibody, prenyl (solanesyl) diphosphate synthase, subunit 2 antibody, PDSS2 antibody, pdss2 antibody, CpipJ_CPIJ016311 antibody, SJAG_01865 antibody, Tsp_08290 antibody, Pdss2 antibody
    背景
    The protein encoded by this gene is an enzyme that synthesizes 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. Defects in this gene are a cause of coenzyme Q10 deficiency.
    分子量
    44 kDa
    NCBI登录号
    NP_065114
    UniProt
    Q86YH6
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