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Signal Transduction Protein Trafficking Vesicle Transport Regulation

Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)

Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR20172] to Nucleophosmin (citrulline R196) - BSA and Azide free
  • Suitable for: Dot blot, WB, IP
  • Reacts with: Mouse, Rat, Human

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Overview

  • Product name

    Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free
    See all Nucleophosmin primary antibodies
  • Description

    Rabbit monoclonal [EPR20172] to Nucleophosmin (citrulline R196) - BSA and Azide free
  • Host species

    Rabbit
  • Tested applications

    Suitable for: Dot blot, WB, IPmore details
  • Species reactivity

    Reacts with: Mouse, Rat, Human
  • Immunogen

    Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.

  • General notes

    Ab251484 is the carrier-free version of ab208015. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.

     

    Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.

    Use our conjugation kits  for antibody conjugates that are ready-to-use in as little as 20 minutes with

    ab251484 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.

    Maxpar® is a trademark of Fluidigm Canada Inc.

    This product is a recombinant monoclonal antibody, which offers several advantages including:

    • - High batch-to-batch consistency and reproducibility
    • - Improved sensitivity and specificity
    • - Long-term security of supply
    • - Animal-free production
    For more information see here.

    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C. Do Not Freeze.
  • Storage buffer

    pH: 7.2
    Constituent: PBS
  • Carrier free

    Yes
  • Concentration information loading...
  • Clonality

    Monoclonal
  • Clone number

    EPR20172
  • Isotype

    IgG
  • Research areas

    • Epigenetics and Nuclear Signaling
    • DNA / RNA
    • Translation
    • Regulation

Images

  • Western blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    Western blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    All lanes : Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] (ab208015) at 1/1000 dilution

    Lane 1 : NIH/3T3 (mouse embryo fibroblast cell line) transfected with a control vector containing GFP tag, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate
    Lane 2 : NIH/3T3 transfected with GFP-tagged PADI4 (WT) expression vector, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate

    Lysates/proteins at 10 µg per lane.

    Developed using the ECL technique.

    Predicted band size: 32 kDa
    Observed band size: 37 kDa
    why is the actual band size different from the predicted?


    Exposure time: 15 seconds


    This data was developed using ab208015, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

    The blot was developed on a BIO-RAD® ChemiDoc™ MP instrument.

  • Western blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    Western blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    All lanes : Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] (ab208015) at 1/1000 dilution

    Lane 1 : HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) transfected with a control vector containing GFP tag, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate
    Lane 2 : HEK-293T transfected with GFP-tagged PADI2 (WT) expression vector, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate
    Lane 3 : C6 (rat glial tumor cell line) transfected with a control vector containing GFP tag, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate
    Lane 4 : C6 transfected with GFP-tagged PADI4 (WT) expression vector, treated with 10 mM calcium chloride and 10 µM Ionomycin for 2 hours, whole cell lysate

    Lysates/proteins at 20 µg per lane.

    Developed using the ECL technique.

    Predicted band size: 32 kDa
    Observed band size: 37 kDa why is the actual band size different from the predicted?



    This data was developed using ab208015, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

    Exposure times: Lanes 1-2: 5 seconds; Lanes 3-4: 3 minutes.

  • Immunoprecipitation - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    Immunoprecipitation - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    This data was developed using ab208015, the same antibody clone in a different buffer formulation.Nucleophosmin (citrulline R196) was immunoprecipitated from 0.35 mg of HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) transfected with GFP-tagged PADI4 expression vector for 24h then treated with 10 mM CaCl2 and 10 µM ionomycin for 2h, whole cell lysate with ab208015 at 1/30 dilution. Western blot was perfromed from the immunoprecipitate using ab208015 at 1/5000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used for detection at 1/10000 dilution. Lane 1: HEK-293T transfected with GFP-tagged PADI4 expression vector for 24h then treated with 10 mM CaCl2 and 10 µM ionomycin for 2h, whole cell lysate 10μg (Input). Lane 2: ab208015 IP in HEK-293T transfected with GFP-tagged PADI4 expression vector for 24h then treated with 10 mM CaCl2 and 10 µM ionomycin for 2h, whole cell lysate. Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab208015 in HEK-293T transfected with GFP-tagged PADI4 expression vector for 24h then treated with 10mM CaCl2 and 10 µM ionomycin for 2h, whole cell lysate. Blocking and dilution buffer and concentration: 5% NFDM/TBST Exposure time : lesss than 1 second.
  • Dot Blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    Dot Blot - Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    This data was developed using ab208015, the same antibody clone in a different buffer formulation.Dot blot analysis of Nucleophosmin (citruline R196) labeled with ab208015 at 1/1000 dilution. Lane 1: Nucleophosmin (citrulline R196) peptide. Lane 2: Nucleophosmin non-citrulline peptide. Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution was used as secondary antibody. Blocking/Dilution buffer: 5% NFDM/TBST. Exposure time: 3 minutes.
  • Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)
    Anti-Nucleophosmin (citrulline R196) antibody [EPR20172] - BSA and Azide free (ab251484)

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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