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Anti-PON1 抗体 [17A12] (ab24261)

Reviews (1)Q&A (6)References (25)
Western blot - Anti-PON1 antibody [17A12] (ab24261)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PON1 antibody [17A12] (ab24261)
  • Flow Cytometry - Anti-PON1 antibody [17A12] (ab24261)
  • Immunocytochemistry/ Immunofluorescence - Anti-PON1 antibody [17A12] (ab24261)
  • Western blot - Anti-PON1 antibody [17A12] (ab24261)

Key features and details

  • Mouse monoclonal [17A12] to PON1
  • Suitable for: ICC/IF, IHC-P, WB, Flow Cyt
  • Reacts with: Human
  • Isotype: IgG1

リコンビナント抗体で、ロット間での高い再現性を実現

Product image
Anti-PON1 antibody [EPR2892] (ab92466)
  • 異なるロット間での安定した再現性
  • 容易なスケールアップ
  • 評価試験による特異性の確認済み
  • 倫理基準に準拠 - アニマル・フリーの生産

製品の概要

  • 製品名

    Anti-PON1 antibody [17A12]
    PON1 一次抗体 製品一覧

  • 製品の詳細

    Mouse monoclonal [17A12] to PON1

  • 由来種

    Mouse

  • アプリケーション

    適用あり: ICC/IF, IHC-P, WB, Flow Cytmore details

  • 種交差性

    交差種: Human
    交差が予測される動物種: Rabbit

  • 免疫原

    Recombinant full length protein (His-tag) corresponding to Human PON1. His tagged recombinant Human PON1 protein purified E.coli.

  • ポジティブ･コントロール

    • IHC-P: Human liver tissue. Flow Cyt: HepG2 cells. ICC/IF: HeLa cells. WB: HeLa and A431 cell lysates.

  • 特記事項

    This product was changed from ascites to tissue culture supernatant on 18th September 2017. Lot numbers higher than GR202765 will be from tissue culture supernatant. Please note that the dilutions may need to be adjusted accordingly.

    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

アプリケーション

The Abpromise guarantee

Abpromise保証は、 次のテスト済みアプリケーションにおけるab24261の使用に適用されます

アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。

アプリケーション Abreviews 特記事項
ICC/IF
Use at an assay dependent concentration.
IHC-P
Use at an assay dependent concentration.
WB (1)
Use a concentration of 2 µg/ml. Predicted molecular weight: 40 kDa.
Flow Cyt
Use at an assay dependent concentration.

ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.
特記事項
ICC/IF
Use at an assay dependent concentration.
IHC-P
Use at an assay dependent concentration.
WB
Use a concentration of 2 µg/ml. Predicted molecular weight: 40 kDa.
Flow Cyt
Use at an assay dependent concentration.

ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.

ターゲット情報

  • 機能

    Hydrolyzes the toxic metabolites of a variety of organophosphorus insecticides. Capable of hydrolyzing a broad spectrum of organophosphate substrates and lactones, and a number of aromatic carboxylic acid esters. Mediates an enzymatic protection of low density lipoproteins against oxidative modification and the consequent series of events leading to atheroma formation.

  • 組織特異性

    Plasma, associated with HDL (at protein level). Expressed in liver, but not in heart, brain, placenta, lung, skeletal muscle, kidney or pancreas.

  • 関連疾患

    Genetic variation in PON1 is associated with susceptibility to microvascular complications of diabetes type 5 (MVCD5) [MIM:612633]. These are pathological conditions that develop in numerous tissues and organs as a consequence of diabetes mellitus. They include diabetic retinopathy, diabetic nephropathy leading to end-stage renal disease, and diabetic neuropathy. Diabetic retinopathy remains the major cause of new-onset blindness among diabetic adults. It is characterized by vascular permeability and increased tissue ischemia and angiogenesis. Note=Homozygosity for the Leu-54 allele is strongly associated with the development of retinal disease in diabetic patients.

  • 配列類似性

    Belongs to the paraoxonase family.

  • 翻訳後修飾

    Glycosylated.
    The signal sequence is not cleaved.
    Present in two forms, form B contains a disulfide bond, form A does not.

  • 細胞内局在

    Secreted > extracellular space.
  • Information by UniProt

  • 参照データベース

    • 別名

      • A esterase 1 antibody
      • A-esterase 1 antibody
      • Aromatic esterase 1 antibody
      • Arylesterase 1 antibody
      • Arylesterase B type antibody
      • ESA antibody
      • Esterase A antibody
      • K 45 antibody
      • K-45 antibody
      • MVCD5 antibody
      • Paraoxonase 1 antibody
      • Paraoxonase antibody
      • Paraoxonase B type antibody
      • Paraoxonase, plasma antibody
      • Paraoxonase1 antibody
      • PON 1 antibody
      • PON antibody
      • PON1 antibody
      • PON1_HUMAN antibody
      • Serum aryldiakylphosphatase antibody
      • Serum aryldialkylphosphatase 1 antibody
      • Serum paraoxonase/arylesterase 1 antibody
      see all

    画像

    • Western blot - Anti-PON1 antibody [17A12] (ab24261)
      Western blot - Anti-PON1 antibody [17A12] (ab24261)
      All lanes : Anti-PON1 antibody [17A12] (ab24261) at 2 µg/ml

      Lane 1 : HeLa (human epithelial cell line from cervix adenocarcinoma) cell lysate
      Lane 2 : A431 (human epidermoid carcinoma cell line) cell lysate

      Secondary
      All lanes : Goat Anti-Mouse IgG at 1/5000 dilution

      Predicted band size: 40 kDa


      Exposure time: 1 minute
    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PON1 antibody [17A12] (ab24261)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PON1 antibody [17A12] (ab24261)
      ab24261 (1µg/ml) staining PON1 in human liver using an automated system (DAKO Autostainer Plus). Using this protocol there is strong cytoplasmic staining of hepatocytes.
      Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer citrate pH 6.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
    • Flow Cytometry - Anti-PON1 antibody [17A12] (ab24261)
      Flow Cytometry - Anti-PON1 antibody [17A12] (ab24261)

      Overlay histogram showing HepG2 cells stained with ab24261 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab24261, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HepG2 cells fixed with 100% methanol (5 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.

    • Immunocytochemistry/ Immunofluorescence - Anti-PON1 antibody [17A12] (ab24261)
      Immunocytochemistry/ Immunofluorescence - Anti-PON1 antibody [17A12] (ab24261)

      ICC/IF image of ab24261 stained HeLa cells. 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 (ab24261, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

    • Western blot - Anti-PON1 antibody [17A12] (ab24261)
      Western blot - Anti-PON1 antibody [17A12] (ab24261)
      Anti-PON1 antibody [17A12] (ab24261) at 1/500 dilution + Recombinant Human PON1 protein (ab53376) at 0.01 µg

      Secondary
      Goat Anti-Mouse IgG H&L (HRP) preadsorbed (ab97040) at 1/500 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 40 kDa


      Exposure time: 1 minute

    参考文献 (25)

    ab24261 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

    ab24261 は 25 報の論文で使用されています。

    • Schilcher I  et al. Endothelial Lipase Modulates Paraoxonase 1 Content and Arylesterase Activity of HDL. Int J Mol Sci 22:N/A (2021). PubMed: 33450841
    • Begue F  et al. Altered high-density lipoprotein composition and functions during severe COVID-19. Sci Rep 11:2291 (2021). PubMed: 33504824
    • Zhao XJ  et al. Hepatic paraoxonase 1 ameliorates dysfunctional high-density lipoprotein and atherosclerosis in scavenger receptor class B type I deficient mice. Ann Transl Med 9:1063 (2021). PubMed: 34422975
    • Gangwar A  et al. Intermittent hypoxia modulates redox homeostasis, lipid metabolism associated inflammatory processes and redox post-translational modifications: Benefits at high altitude. Sci Rep 10:7899 (2020). PubMed: 32404929
    • Tan W  et al. Improvement of Endothelial Dysfunction of Berberine in Atherosclerotic Mice and Mechanism Exploring through TMT-Based Proteomics. Oxid Med Cell Longev 2020:8683404 (2020). PubMed: 32566106
    View all Publications for this product

    レビューと Q&A

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    1-7 of 7 Abreviews or Q&A

    Western blot abreview for Anti-PON1 antibody [17A12]

     Excellent
    Abreviews
    abreview image
    Application
    Western blot
    Sample
    Hamster Tissue lysate - whole (Hamster (Mesocricetus auratus) liver)
    Gel Running Conditions
    Reduced Denaturing (10% SDS-PAGE)
    Loading amount
    60 µg
    Treatment
    Western diet (N normal, HL hyperlipemic), 16 weeks
    Specification
    Hamster (Mesocricetus auratus) liver
    Blocking step
    Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 22°C
    Read More

    DR. Anca Sima

    Verified customer

    投稿 May 21 2015

    Question

    It will be Elisa and PON is antibody , i.e. ab24261

    Read More
    Answer

    Thank you for contacting us.

    I can confirm that antibody ab24261 can be used in ELISA (Indirect) with human cell lysates/ proteins.

    I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information.

    Use our products? Submit an Abreview. Earn rewards!
    https://www.abcam.com/abreviews

    Read More

    Question

    What is the concentration of HEPES in the buffer?

    Read More
    Answer

    Thank you for your phone call yesterday, and I apologize that we did not already have this information. I have heard back from the lab, and the buffer of ab24261 contains 10 mM HEPES. I hope this information is helpful, but please let me know if you have any further questions.

    Read More

    Question

    I'd like to detect human PON1 protein expressed in the liver. But PON2 and PON3 are also expressed in the liver, so I need to use a PON1 specific antibody that don't cross-react to PON2 or PON3. Do you habe any information on the cross-reactibity of your 6 anti-PON1 antibodies with PON2 and PON3? Which product do you recommend for my purpose?　Thank you.

    Read More
    Answer

    Sorry for the long wait. I have another update about one of the products you previously enquired. ab26930: We have not tested this product for cross reactivity with PON2 and PON3. ab24261: There is no reply from the originator and I would assume that they too have not tested the product for cross reactivity with PON2 and PON3. I am sorry I can't be of much help in this occasion but I hope that the information for ab92466 was sufficient for you to use the product in your research. If there is anything else that I can help you with, please do not hesitate to contact me.

    Read More

    Question

    BATCH NUMBER -- NOT SPECIFIED -- ORDER NUMBER -- NOT SPECIFIED -- DESCRIPTION OF THE PROBLEM No signal or weak signal SAMPLE tissue extract PRIMARY ANTIBODY abcam/mouse monoclonal/TBS/1:500 and 1:1000/1 Hour / overnight / 3 washes with TBST for 15 minutes . DETECTION METHOD ECL POSITIVE AND NEGATIVE CONTROLS USED Positive control (Heela cells, plasma) SAMPLE PREPARATION 50 mM phosphate buffer saline pH 7.4/ heating for 3 minutes at 100C AMOUNT OF PROTEIN LOADED 60 ug ELECTROPHORESIS/GEL CONDITIONS SDS-PAGE/12% reducing gel TRANSFER AND BLOCKING CONDITIONS transfer buffer(tris, boric acid, EDTA)/3hrs. blocking agent (5% Non-fat milk/5% BSA) SECONDARY ANTIBODY [another company] / horse / TBS / 1:2000/ 1 hour / 3 washes with TBST for 15 minutes. HOW MANY TIMES HAVE YOU TRIED THE APPLICATION? 6 HAVE YOU RUN A "NO PRIMARY" CONTROL? Yes DO YOU OBTAIN THE SAME RESULTS EVERY TIME? Yes WHAT STEPS HAVE YOU ALTERED? transfer time (1 hr. and 3HR.)/anti body incubation time / anti body dilution / chnging blocking agent (BSA and non- fat milk) ADDITIONAL NOTES we did not get any band in positive control (Heela cell , plasma) as well

    Read More
    Answer

    I'm sorry to hear you are experiencing poor results with ab24261 in western blotting. Your protocol seems good in general and I have only a few suggestions which I help with resolve the problem: -As you are using a good positive control of HeLa cell lysate the problem does not seem to be low expression levels in this sample, however it would be worth trying a different lysis buffer as currently the buffer you use does not seem to be suitable for optimal extraction of the protein. I would therefore recommend using 20 mM Tris-HCl, pH 7.5, 1 mM EGTA and adding protease inhibitors to the buffer. Following lysis and centrifugation I would recommend to add reducing loading buffer to the supernatant and boiling for 5 min at 100C. -I am not familiar with the use of boric acid and EDTA in transfer buffers. We typically use a Tris transfer buffer made with 20% methanol and I would recommend to try this type of buffer. -it is good that you tried different blocking agents. Can I please make sure that you have tried blocking 1 hour only and incubating the antibody overnight in TBST only as sometimes the antibody binds the blocking agent rather than the membrane, if incubated too long together. -it would be worth checking that your transfer is working adequately by doing a Ponceau staining. I hope the suggestions above will help you. Please do not hesitate to contact me if those changes do not give you a better signal and I would be happy to offer you a replacement vial or refund if the antibody was purchased in the last 120 days.

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    Question

    I already purchased PON1 antibody. I would like to know it is rasied against what peptide sequence.

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    Answer

    Thank you for your enquiry. This product has been raised against the full length recombinant form of the target. I hope that this information helps.

    Read More

    Question

    It says that the antibody cross reacts with Mouse PON1. What is the epitope that the antibody recognizes, and how similar is the detection, ie: will 5?g of hPON1 give the same response with chemiluminescence as mPON1?

    Read More
    Answer

    Thank you for your enquiry. The antibody ab2461 has been tested in human samples of HeLa cell lysate and HepG2 cell lysate and in mouse samples on mouse liver tissue lysate on different gels therefore we cannot compare the amount of PON1 protein detected in those samples. In our hands the antibody works very well for both species, I hope this information will help you, please do not hesitate to contact me again if I can be of further assistance,

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