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FDPS 抗体 (AA 201-300) (HRP)

FDPS 适用: 大鼠 ELISA, IHC (p), IHC (fro) 宿主: 兔 Polyclonal HRP
产品编号 ABIN1712050
发货至: 中国
  • 抗原 See all FDPS 抗体
    FDPS (Farnesyl Diphosphate Synthase (FDPS))
    抗原表位
    • 14
    • 9
    • 8
    • 7
    • 7
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 201-300
    适用
    • 51
    • 27
    • 12
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    大鼠
    宿主
    • 60
    • 7
    克隆类型
    • 62
    • 5
    多克隆
    标记
    • 28
    • 6
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This FDPS antibody is conjugated to HRP
    应用范围
    • 40
    • 29
    • 14
    • 13
    • 13
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    交叉反应
    大鼠
    预测反应
    Human,Mouse,Dog,Cow,Sheep,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human FDPS
    亚型
    IgG
    Top Product
    Discover our top product FDPS Primary Antibody
  • 应用备注
    IHC-P 1:200-400
    IHC-F 1:100-500
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    注意事项
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    FDPS (Farnesyl Diphosphate Synthase (FDPS))
    别名
    FDPS (FDPS 产品)
    别名
    CG12389 antibody, DmFPPS antibody, DmFPPSase antibody, DmFPS antibody, Dmel\\CG12389 antibody, FPS antibody, fpps antibody, fps antibody, l(2)k06103 antibody, v(2)k03514 antibody, NCU01175.1 antibody, 16.m00760 antibody, DDBDRAFT_0206220 antibody, DDBDRAFT_0215017 antibody, DDB_0206220 antibody, DDB_0215017 antibody, FPPS antibody, Ac2-125 antibody, (2E antibody, 6030492I17Rik antibody, AI256750 antibody, Fdpsl1 antibody, mKIAA1293 antibody, Farnesyl pyrophosphate synthase antibody, farnesyl diphosphate synthase antibody, farnesyl diphosphate synthase L homeolog antibody, farnesyl pyrophosphate synthase antibody, farnesyl pyrophosphate synthetase antibody, farnesyl-pyrophosphate synthetase antibody, FDP synthase antibody, Farnesyl pyrophosphate synthetase antibody, farnesyl diphosphate synthetase antibody, farnesyl pyrophosphate synthase 1 antibody, Fpps antibody, fdps antibody, fdps.L antibody, MGG_08649 antibody, TP03_0857 antibody, Tb09.160.4300 antibody, fpp antibody, BBOV_I000120 antibody, fps antibody, fpps antibody, FDPS antibody, Fdps antibody, fps1 antibody
    背景

    Synonyms: 2E,6E farnesyl diphosphate synthase, 6E-farnesyl diphosphate synthase, Dimethylallyltranstransferase, Farnesyl diphosphate synthase, Farnesyl diphosphate synthetase, Farnesyl pyrophosphate synthase, Farnesyl pyrophosphate synthetase, Fdps, FPP synthase, FPP synthetase, FPPS, FPPS_HUMAN, FPS, Geranyltranstransferase.

    Background: FDPS is a 419 amino acid enzyme belonging to the FPP/GGPP synthetase family. Localized to cytoplasm and peroxisome, FDPS expression is regulated by phorbol esters and polyunsaturated fatty acids. FDPS assists in cholesterol biosynthesis, post-translational protein modifications and synthesis of steroid hormones in the isoprenoid pathway.FDPS catalyzes the formation of farnesyl diphosphate (FPP), a precursor for several classes of essential metabolites including sterols, dolichols, carotenoids, and ubiquinones. FDPS is inactivated by interferon-induced RSAD2, which may result in the disruption of lipid rafts at the plasma membrane. Existing as a homodimer, FDPS may have anti-viral effects when inactivated by RSAD2. Reduced activity of FDPS in liver may partly be the cause of Zellweger syndrome and neonatal adrenoleukodystrophy, both of which are known to be peroxisomal deficiency diseases.

    基因ID
    2224
    途径
    Regulation of Muscle Cell Differentiation
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