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Anti-HIF-2-alpha 抗体 [ep190b] (ab8365)

Reviews (5)Q&A (18)References (66)
Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)
  • Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)

Key features and details

  • Mouse monoclonal [ep190b] to HIF-2-alpha
  • Suitable for: WB
  • Reacts with: Human
  • Isotype: IgG1

製品の概要

  • 製品名

    Anti-HIF-2-alpha antibody [ep190b]
    HIF-2-alpha 一次抗体 製品一覧

  • 製品の詳細

    Mouse monoclonal [ep190b] to HIF-2-alpha

  • 由来種

    Mouse

  • アプリケーション

    適用あり: WBmore details

  • 種交差性

    交差種: Human
    交差が予測される動物種: Rat

  • 免疫原

    Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.

  • ポジティブ･コントロール

    • WB: Hypoxic A549 and HeLa cell lysate.

  • 特記事項

    This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.

    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

製品の特性

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ab8365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
WB (3)
Use a concentration of 1 µg/ml. Predicted molecular weight: 100 kDa.

Abcam recommends using a 3% milk block with this product.
特記事項
WB
Use a concentration of 1 µg/ml. Predicted molecular weight: 100 kDa.

Abcam recommends using a 3% milk block with this product.

ターゲット情報

  • 機能

    Transcription factor involved in the induction of oxygen regulated genes. Binds to core DNA sequence 5'-[AG]CGTG-3' within the hypoxia response element (HRE) of target gene promoters. Regulates the vascular endothelial growth factor (VEGF) expression and seems to be implicated in the development of blood vessels and the tubular system of lung. May also play a role in the formation of the endothelium that gives rise to the blood brain barrier. Potent activator of the Tie-2 tyrosine kinase expression. Activation seems to require recruitment of transcriptional coactivators such as CREBPB and probably EP300. Interaction with redox regulatory protein APEX seems to activate CTAD.

  • 組織特異性

    Expressed in most tissues, with highest levels in placenta, lung and heart. Selectively expressed in endothelial cells.

  • 関連疾患

    Defects in EPAS1 are the cause of erythrocytosis familial type 4 (ECYT4) [MIM:611783]. ECYT4 is an autosomal dominant disorder characterized by increased serum red blood cell mass, elevated hemoglobin concentration and hematocrit, and normal platelet and leukocyte counts.

  • 配列類似性

    Contains 1 basic helix-loop-helix (bHLH) domain.
    Contains 1 PAC (PAS-associated C-terminal) domain.
    Contains 2 PAS (PER-ARNT-SIM) domains.

  • 翻訳後修飾

    In normoxia, is probably hydroxylated on Pro-405 and Pro-531 by EGLN1/PHD1, EGLN2/PHD2 and/or EGLN3/PHD3. The hydroxylated prolines promote interaction with VHL, initiating rapid ubiquitination and subsequent proteasomal degradation. Under hypoxia, proline hydroxylation is impaired and ubiquitination is attenuated, resulting in stabilization.
    In normoxia, is hydroxylated on Asn-847 by HIF1AN thus probably abrogating interaction with CREBBP and EP300 and preventing transcriptional activation.
    Phosphorylated on multiple sites in the CTAD.
    The iron and 2-oxoglutarate dependent 3-hydroxylation of asparagine is (S) stereospecific within HIF CTAD domains.

  • 細胞内局在

    Nucleus.
  • Information by UniProt

  • 参照データベース

    • 別名

      • Basic helix loop helix PAS protein MOP2 antibody
      • Basic-helix-loop-helix-PAS protein MOP2 antibody
      • bHLHe73 antibody
      • Class E basic helix-loop-helix protein 73 antibody
      • ECYT4 antibody
      • Endothelial PAS domain containing protein 1 antibody
      • Endothelial pas domain protein 1 antibody
      • Endothelial PAS domain-containing protein 1 antibody
      • EPAS 1 antibody
      • EPAS-1 antibody
      • EPAS1 antibody
      • EPAS1_HUMAN antibody
      • HIF 1 alpha like factor antibody
      • HIF 2 alpha antibody
      • HIF-1-alpha-like factor antibody
      • HIF-2-alpha antibody
      • HIF2-alpha antibody
      • HIF2A antibody
      • HLF antibody
      • Hypoxia inducible factor 2 alpha antibody
      • Hypoxia inducible factor 2 alpha subunit antibody
      • Hypoxia-inducible factor 2-alpha antibody
      • Member of PAS protein 2 antibody
      • Member of pas superfamily 2 antibody
      • MOP 2 antibody
      • MOP2 antibody
      • PAS domain-containing protein 2 antibody
      • PASD2 antibody
      see all

    画像

    • Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)
      Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)
      All lanes : Anti-HIF-2-alpha antibody [ep190b] (ab8365) at 1/500 dilution

      Lane 1 : HeLa whole cell lysate
      Lane 2 : HeLa treated with 0.5mM DFO whole cell lysate

      Lysates/proteins at 20 µg per lane.

      Secondary
      All lanes : HRP conjugated Goat Anti-Mouse IgG (H+L) at 1/10000 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 100 kDa
      Observed band size: 100 kDa


      Exposure time: 20 minutes


      This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 55 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with ab8365 overnight at 4°C. Antibody binding was detected using a Goat anti-mouse antibody conjugated to HRP, and visualised using ECL development solution ab133406.

    • Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)
      Western blot - Anti-HIF-2-alpha antibody [ep190b] (ab8365)

      HIF-2-alpha detected in hypoxic Human lysate using ab8365. Lane 1: normoxic A549 lysate control, lane 2: hypoxic A549 lysate.

    参考文献 (66)

    ab8365 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。

    ab8365 は 66 報の論文で使用されています。

    • Morin A  et al. TET-Mediated Hypermethylation Primes SDH-Deficient Cells for HIF2a-Driven Mesenchymal Transition. Cell Rep 30:4551-4566.e7 (2020). PubMed: 32234487
    • Rodrigues T  et al. GLP-1 improves adipose tissue glyoxalase activity and capillarization improving insulin sensitivity in type 2 diabetes. Pharmacol Res 161:105198 (2020). PubMed: 32942016
    • Guo X  et al. Whole-exome sequencing and immunohistochemistry findings in von Hippel-Lindau disease. Mol Genet Genomic Med 7:e880 (2019). PubMed: 31317677
    • Cho C  et al. Cirsium japonicum var. maackii and apigenin block Hif-2a-induced osteoarthritic cartilage destruction. J Cell Mol Med 23:5369-5379 (2019). PubMed: 31148341
    • Polívka J  et al. IDH1 mutation is associated with lower expression of VEGF but not microvessel formation in glioblastoma multiforme. Oncotarget 9:16462-16476 (2018). IHC-P ; Human . PubMed: 29662659
    View all Publications for this product

    レビューと Q&A

    Show All レビュー Q&A
    レビューを送る 質問を送る

    1-10 of 23 Abreviews or Q&A

    Western blot abreview for Anti-HIF-2-alpha antibody [ep190b]

     Inconclusive
    Abreviews
    abreview image
    Application
    Western blot
    Sample
    Rat Tissue lysate - whole (Kidney)
    Gel Running Conditions
    Reduced Denaturing
    Loading amount
    30 µg
    Specification
    Kidney
    Blocking step
    Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: RT°C
    Read More

    Abcam user community

    Verified customer

    投稿 Jun 12 2019

    Immunocytochemistry/ Immunofluorescence abreview for Anti-HIF-2-alpha antibody [ep190b]

     Excellent
    Abreviews
    abreview image
    Application
    Immunocytochemistry/ Immunofluorescence
    Sample
    Mouse Cell (Peritonei tumor)
    Specification
    Peritonei tumor
    Blocking step
    BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 1% · Temperature: RT°C
    Fixative
    Paraformaldehyde
    Read More

    Abcam user community

    Verified customer

    投稿 Jan 19 2016

    Immunocytochemistry/ Immunofluorescence abreview for Anti-HIF-2-alpha antibody [ep190b]

     Good
    Abreviews
    abreview image
    Application
    Immunocytochemistry/ Immunofluorescence
    Sample
    Human Cell (Tumor tisse)
    Permeabilization
    No
    Specification
    Tumor tisse
    Blocking step
    BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 1% · Temperature: RT°C
    Fixative
    Paraformaldehyde
    Read More

    Abcam user community

    Verified customer

    投稿 Sep 29 2015

    Western blot abreview for Anti-HIF-2-alpha antibody [ep190b]

     Average
    Abreviews
    abreview image
    Application
    Western blot
    Loading amount
    50 µg
    Gel Running Conditions
    Reduced Denaturing (4-12% acrylamide)
    Sample
    Human Cell lysate - whole cell (Renal cancer cell line)
    Specification
    Renal cancer cell line
    Blocking step
    Li-cor Blocking Buffer PBS as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
    Read More

    Abcam user community

    Verified customer

    投稿 Jul 28 2014

    Question

    I am using Primary human cutaneous melanoma tissue. And they were paraffin
    samples. I placed sections in Sodium citrate in a plastic-screw top container
    and heat at 95C in boiling water for 30mins. Cool down in room temp for 20
    mins, and rinse sections in PBS: 3 times for 5mins.
    For the antibody dilutions: 1:25, 1:50, 1:100, 1:200. For blocking I used
    protein blocker. And the secondary antibody is provided from another company. And
    other primaries does works well with this secondary antibody.

    Read More
    Answer


    I was wondering, did you try any other antigen retrieval step, such as Tris EDTA (pH 8)? This has been successfully used by another researcher with human breast cancer tissue. I would suggest trying this.

    I am not sure how long you incubated with the primary antibody, but if overnight incubation has not yet been tried, I would suggest trying this as well.

    Read More

    Question


    I would like to know does the HIF-2a antibody comes with a guarantee
    (Anti-HIF2 alpha antibody [ep190b] (ab8365)? Can we refund the Product in case
    the antibody doesn't work? Thanks.

    Read More
    Answer

    Thank you for contacting us.

    We guarantee ab8365 to work in Flow Cyt, ELISA, IHC-Fr, IHC-P, WB with rat and human samples in accordance with our Abpromise. If you have difficulty in these applications and species, let us know and we will refund or replace the product for you within 6 months of purchase.

    https://www.abcam.com/index.html?pageconfig=resource&rid=10372&pid=10000&source=pagetrap

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

    Read More

    Question

    No signal in IHC-Fr human samples. Used ab at 1ug/ml.
    What was the protocol used to test this ab in IHC-Fr?

    Read More
    Answer

    Thank you for your patience whilst I have been trying to contact our supplier to get the protocol they used to test ab8365 in IHC-Fr. Unfortunately they are unable to provide that information, therefore I think the best course of action is to either replace or refund the antibody for you.

    Please let me know how you would you like to continue and if you could also provide either the Abcam order number or the PO# used to purchase the antibody that would be very helpful.

    I look forward to your reply and I do apologize for the delay in responding to you.

    Read More

    Question

    Dear technical team,

    Our customer would like to purchase HIF2 alpha antibody with mouse monoclonal host to test WB and IHC-P.

    She searched ab8365 and wants to confirm it detects endogeneous HIF2 alpha.

    Check this please.

    Best regards,

    Read More
    Answer

    Thank you for your enquiry and your interest in our products.

    I can confirm that this antibody (ab8365: Anti-HIF2 alpha antibody) has been tested for IHC-Fr, IHC-P, WB, please take a look at the datasheet under tested application and the images.



    ab8365 can detect endogenous HIF2 alpha, however under hypoxia HIF2 alpha is induced and the signal for HIF2 alpha in Western blot is significantly stronger compared to normoxic conditions.

    If you need any further assistance in the future, please do not hesitate to contact me.

    Read More

    Question

      Thank you for your answer. Indeed the staining we obtained seems very specific, specially in the cytoplasm of the human kidney biopsies (formalin-fixed). Unfortunately we still don’t have photos because our microscope doesn’t have a camera and we have to take the slides to another institute.  My doubt is: if Hif-2 alpha is extremely rapidly degraded, how can it be staining in the cytoplasm? Shouldn’t I have no signal at all? Or can I assume that when the cells are in normoxia I detect HIF-2alpha in the cytoplasm?   To answer your question about the hypoxia conditions, we maintained the HEK cells in 200 µM CoCl2 for 6 hours to try to mimic hypoxia.  In attachment I’m sending the questionnaire filled out. If you have any more doubts please feel free to ask. Unfortunately this antibody has been purchased more than 6 months ago but It hadn’t been tested until two months ago because I was out from the lab. Anyway, the important is to be sure that the staining I'm having is specific for HIF-2alpha.  Best regards,     

    Read More
    Answer

    Thank you very much for your answer. I am sorry, I think I am also a little bit confused with the HIF proteins. There are indeed different studies - on particular study showing that in MEFs (i have not found yet a study on HEK cells) the localisation of HIF 2 alpha is mainly cytoplasmic and not inducible. http://mcb.asm.org/cgi/content/full/23/14/4959?view=long&pmid=12832481 The publication here below shows the HIF 2 alpha expression in liver, which seems to be also quite a lot of cytoplasmic staining. http://www.wjgnet.com/1007-9327/full/v16/i3/WJG-16-281-g001.htm Please have a look at these publications (and maybe others, as I am not a specialist with HIF 2 alpha) and let me know whether these might explain the stainings. I have also looked through the protocol provided. It seems very good to me. Can you just confirm what kind of controls you have performed to exclude unspecific staining? Have you performed an isotype control? This would indeed be the best control. I am looking forward to hear back from you with your comments.

    Read More

    Question

    To the Scientific Support team We ordered the monoclonal antibody Hif-2 alpha [ep190b], Ref: ab8365 and we tested it for immunohistochemistry on parafin human kidney bipsies and for immunofluorescence on HEK293T cells both in normoxia and hypoxia. We expected to obtain a nuclear staining but what we obtained was:  1 - in the immunohistochemistry we saw a specific staining in the cytoplasm 2- in the immunofluorescence it seems to be staining both the cytoplasm and nucleus.  I send in attachment some images of the immunofluorescence results. We would like to ask if there is something wrong with this antibody, as it should be staining the nucleus, and if it’s possible to change this antibody for another that works better.  Thank you very much,     

    Read More
    Answer

    Thank you for taking time to contact us. I am sorry to hear that this antibody is not providing satisfactory results. Having reviewed this case, I would like to offer some suggestions to help optimize the results with this antibody. Indeed, HIF 2 alpha is a difficult target to work with. I suspect that the observed staining is indeed the real staining. Upon stabilization HIF translocates to the nucleus. Please also note that Hif-2 alpha is extremely rapidly degraded. Upon cellular re-oxygenation its is completely degraded in less than 1 minute. Please see also the image of the publication, where MEFs have been stained for HIF 2 alpha and substantial cytoplasmic staining is observed. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC162224/?tool=pubmed Additionally, HIF can be difficult to detect in cells or tissues grown under normoxic conditions. Its is stabilized only at O2 concentrations below 5% or with treatment using certain agents (CoCl2, DFO, etc.) so proper sample preparation is critical. Can you please specify what hypoxic conditions have been used to treat the HEK cells? I am looking forward to hear back from you with your comments on the above raised points. I have also attached a questionnaire, which I would be grateful if you could fill it out, so I could look into the problem in more detail. Can you please also attach an image of the kidney staining? Thank you very much! In the event that a product is not functioning in the species and applications cited on the product datasheet (and the problem has been reported within 6 months of purchase), we would be pleased to provide a free of charge replacement, credit note, or refund. I hope this information is helpful, and I thank you for your cooperation.  

    Read More

    1-10 of 23 Abreviews or Q&A

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