製品の概要

  • 製品名Anti-COQ10B antibody
  • 製品の詳細
    Rabbit polyclonal to COQ10B
  • アプリケーション適用あり: IHC-P, WBmore details
  • 種交差性
    交差種: Mouse, Rat, Human
    交差が予測される動物種: Cow, Orangutan
  • 免疫原

    Synthetic peptide conjugated to KLH derived from within residues 50 - 150 of Human COQ10B.

    (Peptide available as ab41996.)

  • ポジティブ・コントロール
    • This antibody gave a positive signal 1n the following lysates: HepG2 Whole Cell HeLa Whole Cell Rat Liver Tissue Mouse Pancreas Tissue Mouse Liver Tissue (data not shown)

製品の特性

アプリケーション

Our Abpromise guarantee covers the use of ab41997 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

アプリケーション Abreviews 特記事項
IHC-P Use a concentration of 5 µg/ml.
WB Use a concentration of 1 µg/ml. Detects a band of approximately 32 kDa (predicted molecular weight: 27 kDa).

ターゲット情報

  • 関連性COQ10 (Coenzyme Q10) is found in a wide variety of foods and is synthesized in all tissues. The de novo biosynthesis of COQ10, from its precursor tyrosine, is a multistage process that requires at least eight vitamins and several trace elements. More complex enzymes have an absolute dependancy on 'cofactors', a large group of molecules to which the coenzymes belong, for their catalyitic function. Coenzyme Q10 is the cofactor for, but not limited to, several mitochondrial enzymes that are central to the supply of adenosine triphosphate (ATP). In addition, COQ10 in its reduced form is a potent antioxidant, and in this capacity, a reduction in COQ10 levels are associtated with a variety of degenerative process including skin aging and neurodegenerative conditions such as Alzhiemer's, Huntingdon's and Parkinson's diseases.
  • 細胞内局在Mitochondrial
  • 参照データベース
  • 別名
    • Coenzyme Q10 antibody
    • Coenzyme Q10 B antibody
    • Coenzyme Q10 homolog B antibody
    • Coenzyme Q10B antibody

Anti-COQ10B antibody 画像

  • All lanes : Anti-COQ10B antibody (ab41997) at 1 µg/ml

    Lane 1 : HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate
    Lane 2 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate
    Lane 3 : Liver (Rat) Tissue Lysate
    Lane 4 : Mouse pancreas tissue lysate - total protein (ab29363)

    Lysates/proteins at 10 µg per lane.

    Secondary
    Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

    Performed under reducing conditions.

    Predicted band size : 27 kDa
    Observed band size : 32 kDa (why is the actual band size different from the predicted?)
  • IHC image of ab41997 staining COQ10B in Human liver formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab41997, 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

    For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
  • ICC/IF image of ab41997 stained HeLa cells. The cells were stained with Mitotracker Orange CMTMRos at a concentration of 500nM in PBS and incubated for 45 minutes at 37°C. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab41997, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Dylight® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

Anti-COQ10B antibody (ab41997) 使用論文

ab41997 has not yet been referenced specifically in any publications.

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