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Anti-Histone H3 (acetyl K18) antibody - ChIP Grade (ab1191)

Overview

  • Product nameAnti-Histone H3 (acetyl K18) antibody - ChIP GradeSee all Histone H3 primary antibodies ...
  • Description
    Rabbit polyclonal to Histone H3 (acetyl K18) - ChIP Grade
  • SpecificitySpecificity for acetyl K18 has been validated by blocking peptide/antibody incubation followed by immunostaining western blots.
  • Tested applicationsWB, CHIPseq, IHC-P, ICC/IF, ChIP/Chip, ChIP more details
  • Species reactivity
    Reacts with: Mouse, Cow, Human, Saccharomyces cerevisiae, Arabidopsis thaliana, Fruit fly (Drosophila melanogaster), Fungi
  • Immunogen

    Synthetic peptide derived from within residues 1 - 100 Histone H3, acetylated at K18.

    (Peptide available as ab24003.)

  • Positive controlThis antibody gave a positive signal in HeLa Histone Preparation Nuclear Lysate. This antibody gave a positive result in IHC in the following FFPE tissue: Human normal skin.

Properties

Applications

Our Abpromise guarantee covers the use of ab1191 in the following tested applications.

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

Application Notes
WB WB: 1/1000. Detects a band of approximately 17 kDa.Can be blocked with Histone H3 peptide - acetyl K18 (ab24003).
CHIPseq CHIPseq: Use at an assay dependent dilution.
IHC-P IHC-P: 1/200.
ICC/IF ICC/IF: Use a concentration of 1 µg/ml.
ChIP/Chip ChIP/Chip: Use at an assay dependent dilution.
ChIP ChIP: Use 2µg for 106 cells.

Target

  • FunctionCore component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling.
  • Sequence similaritiesBelongs to the histone H3 family.
  • Developmental stageExpressed during S phase, then expression strongly decreases as cell division slows down during the process of differentiation.
  • Post-translational
    modifications
    Acetylation is generally linked to gene activation. Acetylation on Lys-10 (H3K9ac) impairs methylation at Arg-9 (H3R8me2s). Acetylation on Lys-19 (H3K18ac) and Lys-24 (H3K24ac) favors methylation at Arg-18 (H3R17me).
    Citrullination at Arg-9 (H3R8ci) and/or Arg-18 (H3R17ci) by PADI4 impairs methylation and represses transcription.
    Asymmetric dimethylation at Arg-18 (H3R17me2a) by CARM1 is linked to gene activation. Symmetric dimethylation at Arg-9 (H3R8me2s) by PRMT5 is linked to gene repression. Asymmetric dimethylation at Arg-3 (H3R2me2a) by PRMT6 is linked to gene repression and is mutually exclusive with H3 Lys-5 methylation (H3K4me2 and H3K4me3). H3R2me2a is present at the 3' of genes regardless of their transcription state and is enriched on inactive promoters, while it is absent on active promoters.
    Methylation at Lys-5 (H3K4me), Lys-37 (H3K36me) and Lys-80 (H3K79me) are linked to gene activation. Methylation at Lys-5 (H3K4me) facilitates subsequent acetylation of H3 and H4. Methylation at Lys-80 (H3K79me) is associated with DNA double-strand break (DSB) responses and is a specific target for TP53BP1. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are linked to gene repression. Methylation at Lys-10 (H3K9me) is a specific target for HP1 proteins (CBX1, CBX3 and CBX5) and prevents subsequent phosphorylation at Ser-11 (H3S10ph) and acetylation of H3 and H4. Methylation at Lys-5 (H3K4me) and Lys-80 (H3K79me) require preliminary monoubiquitination of H2B at 'Lys-120'. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are enriched in inactive X chromosome chromatin.
    Phosphorylated at Thr-4 (H3T3ph) by GSG2/haspin during prophase and dephosphorylated during anaphase. Phosphorylation at Ser-11 (H3S10ph) by AURKB is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. In addition phosphorylation at Ser-11 (H3S10ph) by RPS6KA4 and RPS6KA5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or UV irradiation and result in the activation of genes, such as c-fos and c-jun. Phosphorylation at Ser-11 (H3S10ph), which is linked to gene activation, prevents methylation at Lys-10 (H3K9me) but facilitates acetylation of H3 and H4. Phosphorylation at Ser-11 (H3S10ph) by AURKB mediates the dissociation of HP1 proteins (CBX1, CBX3 and CBX5) from heterochromatin. Phosphorylation at Ser-11 (H3S10ph) is also an essential regulatory mechanism for neoplastic cell transformation. Phosphorylated at Ser-29 (H3S28ph) by MLTK isoform 1, RPS6KA5 or AURKB during mitosis or upon ultraviolet B irradiation. Phosphorylation at Thr-7 (H3T6ph) by PRKCBB is a specific tag for epigenetic transcriptional activation that prevents demethylation of Lys-5 (H3K4me) by LSD1/KDM1A. At centromeres, specifically phosphorylated at Thr-12 (H3T11ph) from prophase to early anaphase, by DAPK3 and PKN1. Phosphorylation at Thr-12 (H3T11ph) by PKN1 is a specific tag for epigenetic transcriptional activation that promotes demethylation of Lys-10 (H3K9me) by KDM4C/JMJD2C. Phosphorylation at Tyr-42 (H3Y41ph) by JAK2 promotes exclusion of CBX5 (HP1 alpha) from chromatin.
    Monoubiquitinated by RAG1 in lymphoid cells, monoubiquitination is required for V(D)J recombination (By similarity). Ubiquitinated by the CUL4-DDB-RBX1 complex in response to ultraviolet irradiation. This may weaken the interaction between histones and DNA and facilitate DNA accessibility to repair proteins.
  • Cellular localizationNucleus. Chromosome.
  • Target information above from: UniProt accession P68431 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Database links
  • Alternative names
      H 3 antibodyH3 3 Like Sequence MH921 antibodyH3 3A antibody
      H3 3A antibodyH3 antibodyH3 Histone antibodyH3 Histone Family Member E Pseudogene antibodyH3.4 antibodyH3/A antibodyH3/g antibodyH31_HUMAN antibodyH3F3 antibodyH3F3 antibodyH3FA antibodyH3FT antibodyH3t antibodyHIST1H3J antibodyHIST3H3 antibodyHIST3H3 antibodyHistone cluster 1, H3a antibodyHistone H3 3 Pseudogene antibodyHistone H3.1 antibodyHistone H3.3 antibodyHistone H3/a antibodyHistone H3/b antibodyHistone H3/c antibodyHistone H3/d antibodyHistone H3/f antibodyHistone H3/h antibodyHistone H3/i antibodyHistone H3/j antibodyHistone H3/k antibodyHistone H3/l antibody
    see all

Anti-Histone H3 (acetyl K18) antibody - ChIP Grade images

  • Chromatin was prepared from U2OS cells according to the Abcam X-ChIP protocol. Cells were fixed with formaldehyde for 10 min. The ChIP was performed with 25 µg of chromatin, 2 µg of ab1191 (blue), and 20 µl of protein A/G sepharose beads. No antibody was added to the beads control (yellow). The immunoprecipitated DNA was quantified by real time PCR (Taqman approach). Primers and probes are located in the first kb of the transcribed region.

  • L929, 3T3 and HeLa cells fixed with 2% paraformaldehyde in PBS were incubated for 5 min in 0.2% Triton X-100 in PBS before a blocking step in 5% BSA, 0.1% Tween 20 in PBS (blocking buffer). Ac K18-H3 (ab1191) antibody was added diluted at 1/500 in blocking buffer for a 45 min incubation at room temperature. For visualization, fluorescein isothiocyanate (FITC) anti rabbit secondary antibody was used diluted at 1/800. DAPI (Sigma) in 0.1% Tween 20 in PBS was used in the final washing steps to stain DNA. Vectashield (Vector Laboratories Inc.) was used as mounting medium.
    The ac K18-H3 antibody revealed a granular staining throughout the nucleoplasm, excluding regions that show an intense DAPI staining (mostly pericentric heterochromatin in mice cells).
  • All lanes : Anti-Histone H3 (acetyl K18) antibody - ChIP Grade (ab1191) at 1 µg/ml

    Lane 1 : Histone prep
    Lane 2 : Histone prep with Histone H3 peptide - acetyl K18 (ab24003) at 1 µg/ml

    Lysates/proteins at 0.5 µg/ml per lane.

    Secondary
    Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP) (ab6721) at 1/5000 dilution

    Predicted band size : 15.4 kDa
    Observed band size : 17 kDa (why is the actual band size different from the predicted?)
  • ICC/IF image of ab1191 stained HeLa cells. The cells were 100% methanol fixed (5 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 (ab1191, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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. This antibody also gave a positive result in 100% methanol fixed (5 min) Hek293, HepG2 and MCF7 cells at 1µg/ml, and in 4% PFA fixed (10 min) HeLa, Hek293, HepG2 and MCF7 cells at 1µg/ml.
  • All lanes : Anti-Histone H3 (acetyl K18) antibody - ChIP Grade (ab1191) at 1 µg/ml

    Lane 1 : HeLa Histone Preparation Nuclear Lysate
    Lane 2 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - unmodified R17 at 0.5 µg/ml
    Lane 3 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K9 (ab16635) at 0.5 µg/ml
    Lane 4 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K14 at 0.5 µg/ml
    Lane 5 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K18 (ab24003) at 0.5 µg/ml
    Lane 6 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K23 (ab48359) at 0.5 µg/ml
    Lane 7 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K27 (ab24404) at 0.5 µg/ml
    Lane 8 : HeLa Histone Preparation Nuclear Lysate with Histone H3 peptide - acetyl K36 at 0.5 µg/ml
    Lane 9 : HeLa Histone Preparation Nuclear Lysate with Histone H4 peptide - acetyl K12 (ab15662) at 0.5 µg/ml

    Lysates/proteins at 2.5 µg per lane.

    Secondary
    Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
    developed using the ECL technique

    Performed under reducing conditions.

    Predicted band size : 15.4 kDa
    Observed band size : 17 kDa (why is the actual band size different from the predicted?)


    Exposure time : 1 minute
  • IHC image of Histone H3 (acetyl K18) staining in Human normal skin 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 ab1191, 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.

References for Anti-Histone H3 (acetyl K18) antibody - ChIP Grade (ab1191)

This product has been referenced in:
  • Holmqvist PH  et al. Preferential Genome Targeting of the CBP Co-Activator by Rel and Smad Proteins in Early Drosophila melanogaster Embryos. PLoS Genet 8:e1002769 (2012). ChIP ; Fruit fly (Drosophila melanogaster) . Read more (PubMed: 22737084) »
  • Genereaux J  et al. Genetic evidence links the ASTRA protein chaperone component Tti2 to the SAGA transcription factor Tra1. Genetics 191:765-80 (2012). ChIP ; Saccharomyces cerevisiae . Read more (PubMed: 22505622) »

See all 27 Publications for this product

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Thank you very much for your call today and for letting us know about the trouble with this antibody.

As we discussed, I'm sending a free of charge vial of ab40888 on the order ***, which should arrive tomorrow.

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I have processed your request to receive a new vial of ab1191, as the one you currently have is not giving you the level of enrichment that you expect in ChIP. Your new order number is ***. Due to the storm on the east ...

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Thank you for providing that information.

I would be happy to send you a new vial of the antibody as the current aliquot you have is not giving the expected results. We do not have any of the lots that you previously used in stock, so I would be...

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For our records could you please also let me know the sample (including species) that you were using the antibody on and also the protocol (including the concentration of the antibody you were using)? Read More


Beide Artikel wurden in Großbritannien hergestellt und haben ein Gewicht von 100ug.

Application Western blot
Sample Saccharomyces cerevisiae Cell lysate - whole cell (s. cerevisiae cells)
Loading amount 10 µg
Specification s. cerevisiae cells
Gel Running Conditions Reduced Denaturing
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 20°C
Username

Verified customer

Submitted Aug 16 2011

Application ChIP
Sample Human Cell lysate - nuclear (5 million LNCaP cells/IP)
Specification 5 million LNCaP cells/IP
Type Cross-linking (X-ChIP)
Duration of cross-linking step: 10 minute(s) and 0 second(s)
Specification of the cross-linking agent: Formaldehyde
Detection step Real-time PCR
Positive control PSA enhancer
Negative control rabbit IgG
Username

Verified customer

Submitted Jul 01 2010

Application ChIP
Sample Human Cell lysate - whole cell (HeLa)
Specification HeLa
Type Cross-linking (X-ChIP)
Duration of cross-linking step: 0 second(s)
Specification of the cross-linking agent: Formaldehyde
Detection step Other
Username

Verified customer

Submitted Nov 30 2006

Application Immunocytochemistry/ Immunofluorescence
Sample Arabidopsis thaliana Cell (Culture cell, ecotype Lansberg)
Specification Culture cell, ecotype Lansberg
Fixative Paraformaldehyde
Blocking step BSA as blocking agent for 1 hour(s) and 30 minute(s) · Concentration: 3%
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Verified customer

Submitted Aug 04 2006

Thank you for your enquiry. Details of the positive controls for these histone antibodies are not detailed in the datasheet. However, these histone modifications are ubiquitous across all cell types (except yeast which do not have acetylation at lysin...

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