Anti-beta 1 Sodium Potassium ATPase抗体[M17-P5-F11] (ab2873)

概述

  • 产品名称Anti-beta 1 Sodium Potassium ATPase抗体[M17-P5-F11]
    参阅全部 beta 1 Sodium Potassium ATPase 一抗
  • 描述
    小鼠单克隆抗体[M17-P5-F11] to beta 1 Sodium Potassium ATPase
  • 经测试应用适用于: IHC-Fr, IP, WB, IHC-P, ICC/IF, Inhibition Assay, ICC, Flow Cytmore details
  • 种属反应性
    与反应: Mouse, Rat, Sheep, Dog, Human, Pig, Drosophila melanogaster
    预测可用于: Rabbit, Guinea pig, Chimpanzee, Cynomolgus Monkey
  • 免疫原

    Full length native protein (purified) corresponding to Sheep beta Sodium Potassium ATPase. Purified lamb kidney sodium/potassium ATPase beta.

  • 表位This antibody recognizes an epitope between amino acid residues 195-199 of sheep sodium/potassium ATPase beta 1.

性能

应用

Our Abpromise guarantee covers the use of ab2873 in the following tested applications.

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

应用 Ab评论 说明
IHC-Fr 1/100.
IP Use at an assay dependent concentration.
WB 1/250.
IHC-P 1/200.
ICC/IF 1/100 - 1/1000.
Inhibition Assay Use at an assay dependent concentration.
ICC Use at an assay dependent concentration.
Flow Cyt 1/100.

靶标

Anti-beta 1 Sodium Potassium ATPase antibody [M17-P5-F11] 图像

  • Immunocytochemistry/Immunofluorescence analysis of beta 1 Sodium Potassium ATPase shows staining in HeLa cells. beta 1 Sodium Potassium ATPase staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2873 (1:200) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated goat anti-mouse secondary antibody. Images were taken at 60X magnification.

  • Immunocytochemistry/Immunofluorescence analysis of beta 1 Sodium Potassium ATPase shows staining in MCF-7 cells. beta 1 Sodium Potassium ATPase staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2873 (1:200) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated goat anti-mouse secondary antibody. Images were taken at 60X magnification.

  • Immunocytochemistry/Immunofluorescence analysis of beta 1 Sodium Potassium ATPase shows staining in U251 cells. beta 1 Sodium Potassium ATPase staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2873 (1:200) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated goat anti-mouse secondary antibody. Images were taken at 60X magnification.

  • IHC image of ab2873 staining in human normal 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 ab2873, 1µg/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.

  • Overlay histogram showing HEK293 cells stained with ab2873 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab2873, 1/100 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HEK293 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.

    Please note that Abcam do not have any data for use of this antibody on non-fixed cells. We welcome any customer feedback.
  • Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human colon carcinoma tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase beta ab2873 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.

  • Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human liver tissue tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase beta ab2873 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.

  • Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human tonsil tissue tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:200 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase beta ab2873 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.

Anti-beta 1 Sodium Potassium ATPase antibody [M17-P5-F11] (ab2873)参考文献

This product has been referenced in:
  • Marshall DJ  et al. Extracellular Antibody Drug Conjugates Exploiting the Proximity of Two Proteins. Mol Ther N/A:N/A (2016). WB . Read more (PubMed: 27434591) »
  • Seebohm G  et al. Structural basis of PI(4,5)P2-dependent regulation of GluA1 by phosphatidylinositol-5-phosphate 4-kinase, type II, alpha (PIP5K2A). Pflugers Arch 466:1885-97 (2014). Read more (PubMed: 24389605) »

See all 5 Publications for this product

Product Wall

Thank you for your enquiry. ab2873 (Sodium/Potassium ATPase Beta) is not affinity purified but comes as a PBS-diluted ascites containing 0.05% sodium azide. Please do not hesitate to contact me should you require further assistance.

Thank you for your patience. Purified lamb kidney beta sodium/potassium ATPase was used as the immunogen for both ab2871 and ab2873. Further characterization of the epitope region has not yet been performed. Therefore we are unable to determine the lo...

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"