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AGPS 抗体

This anti-AGPS antibody is a 兔 多克隆 antibody detecting AGPS in WB. Suitable for 人.
产品编号 ABIN2854324
发货至: 中国

Quick Overview for AGPS 抗体 (ABIN2854324)

抗原

See all AGPS 抗体
AGPS (Alkylglycerone Phosphate Synthase (AGPS))

适用

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宿主

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克隆类型

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多克隆

标记

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This AGPS antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 交叉反应

    产品特性

    Rabbit Polyclonal antibody to Alkyl-DHAP synthase (alkylglycerone phosphate synthase)
    Alkyl-DHAP synthase antibody

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human Alkyl-DHAP synthase. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: human AGPS-transfected 293T cells , MDA-MB-231

    Validation: Overexpression

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

    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.

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    AGPS (Alkylglycerone Phosphate Synthase (AGPS))

    别名

    alkylglycerone phosphate synthase

    背景

    This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.

    Cellular Localization: Peroxisome membrane

    分子量

    73 kDa

    基因ID

    8540

    UniProt

    O00116

    途径

    SARS-CoV-2 Protein Interactome
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