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Epigenetics and Nuclear Signaling Histones H3 Acetylated

Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)

Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
  • 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

  • Rabbit polyclonal to Histone H2A (acetyl K5) - ChIP Grade
  • Suitable for: Dot blot, ICC/IF, ChIP-sequencing, WB, ChIP
  • Reacts with: Human, Recombinant fragment
  • Isotype: IgG

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Overview

  • Product name

    Anti-Histone H2A (acetyl K5) antibody - ChIP Grade
    See all Histone H2A primary antibodies
  • Description

    Rabbit polyclonal to Histone H2A (acetyl K5) - ChIP Grade
  • Host species

    Rabbit
  • Tested applications

    Suitable for: Dot blot, ICC/IF, ChIP-sequencing, WB, ChIPmore details
  • Species reactivity

    Reacts with: Human, Recombinant fragment
  • Immunogen

    Synthetic peptide within Human Histone H2A (acetyl K5) conjugated to keyhole limpet haemocyanin. The exact sequence is proprietary.

  • Positive control

    • Histone extracts and whole cell extracts from HeLa cells; HeLa cells; chromatin from HeLa and HeLaS3 cells.
  • General notes

    Reproducibility is key to advancing scientific discovery and accelerating scientists’ next breakthrough.

    Abcam is leading the way with our range of recombinant antibodies, knockout-validated antibodies and knockout cell lines, all of which support improved reproducibility.

    We are also planning to innovate the way in which we present recommended applications and species on our product datasheets, so that only applications & species that have been tested in our own labs, our suppliers or by selected trusted collaborators are covered by our Abpromise™ guarantee.

    In preparation for this, we have started to update the applications & species that this product is Abpromise guaranteed for.

    We are also updating the applications & species that this product has been “predicted to work with,” however this information is not covered by our Abpromise guarantee.

    Applications & species from publications and Abreviews that have not been tested in our own labs or in those of our suppliers are not covered by the Abpromise guarantee.

    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, as well as customer reviews and Q&As.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Storage buffer

    Preservatives: 0.05% Sodium azide, 0.05% Proclin 300
    Constituent: 99% PBS
  • Concentration information loading...
  • Purity

    Protein A purified
  • Clonality

    Polyclonal
  • Isotype

    IgG
  • Research areas

    • Epigenetics and Nuclear Signaling
    • Histones
    • H2A
    • Acetylated
    • Epigenetics and Nuclear Signaling
    • ChIP assays
    • ChIP antibodies

Images

  • ChIP-sequencing - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    ChIP-sequencing - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)

    ChIP was performed on sheared chromatin from 1.5 million HeLaS3 cells using 0.5 μg of ab195486. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 51 bp tags were aligned to the human genome using the BWA algorithm. This figure shows the enrichment along the complete sequence and a 1 Mb region of the X-chromosome (panels A and B) and in genomic regions of chromosome 7, surrounding the ACTB gene, and of chromosome 12, surrounding the GAPDH gene (panels C and D). The position of the amplicon used for ChIP-qPCR is indicated by an arrow.

  • Western blot - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    Western blot - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    All lanes : Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486) at 1/1000 dilution

    Lane 1 : whole cell HeLa extracts at 25 µg
    Lane 2 : HeLa histone extracts at 15 µg
    Lane 3 : recombinant histone H2A at 1 µg
    Lane 4 : recombinant histone H2B at 1 µg
    Lane 5 : recombinant histone H3 at 1 µg
    Lane 6 : recombinant histone H4 at 1 µg

    Predicted band size: 14 kDa

  • Immunocytochemistry/ Immunofluorescence - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    Immunocytochemistry/ Immunofluorescence - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)

    Immunofluorescent analysis of HeLa cells (4% formaldehyde-fixed) labeling Histone H2A (acetyl K5) with ab195486 at 1/500 dilution followed by an anti-rabbit antibody conjugated to Alexa488 (left panel). The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.

  • Dot Blot - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    Dot Blot - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)

    Dot Blot analysis was performed to test the cross reactivity of ab195486 against Histone H2A (acetyl K5) with peptides containing other histone modifications and the unmodified H2AK5. One hundred to 0.2 pmol of the respective peptides were spotted on a membrane.  ab195486 was used at 1/5,000 dilution. 

  • ChIP - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)
    ChIP - Anti-Histone H2A (acetyl K5) antibody - ChIP Grade (ab195486)

    ChIP analysis using HeLa cells, ab195486 and optimized PCR primer sets for qPCR. ChIP was performed using sheared chromatin from 1.5 million cells. A titration of the antibody consisting of 0.5, 1, 2 and, 5 µg per ChIP experiment was analysed. IgG (1 µg/IP) was used as negative IP control. QPCR was performed with primers for a region approximately 1 kb upstream of the GAPDH and ACTB promoters, used as positive controls, and for the coding region of the inactive MYOD1 gene and the Sat2 satellite repeat, used as negative controls.

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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