Anti-Histone H2B (mono methyl K5)抗体- ChIP Grade (ab12929)


  • 产品名称
    Anti-Histone H2B (mono methyl K5)抗体- ChIP Grade
    参阅全部 Histone H2B 一抗
  • 描述
    兔多克隆抗体to Histone H2B (mono methyl K5) - ChIP Grade
  • 宿主
  • 特异性
    Mono methylation of Histone H2B K5 is a putative modification site. ab22512 in ELISA specifically recognises mono-methyl K5 histone H2B peptide but not the corresponding unmodified histone H2B peptide.
  • 经测试应用
    适用于: IHC-P, ICC/IF, IP, WB, ChIPmore details
  • 种属反应性
    与反应: Mouse, Rat, Human
    预测可用于: Chicken, Cow, Xenopus laevis
  • 免疫原

    Synthetic peptide within Human Histone H2B aa 1-100 (mono methyl K5) conjugated to Keyhole Limpet Haemocyanin (KLH). The exact sequence is proprietary.
    (Peptide available as ab13211)

  • 阳性对照
    • This antibody gave a positive signal in Calf Thymus Histone Preparation Nuclear Lysate. This antibody gave a positive signal in the following Methanol fixed cell lines: HeLa. It also gave a positive signal in FFPE human pancreatic adenocarcinoma tissue sections.



Our Abpromise guarantee covers the use of ab12929 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-P Use a concentration of 0.1 µg/ml. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
ICC/IF Use at an assay dependent concentration. PubMed: 23240083
IP Use at an assay dependent concentration.
WB Use a concentration of 1 µg/ml. Can be blocked with Human Histone H2B (mono methyl K5) peptide (ab13211).
ChIP Use 2-5 µg for 25 µg of chromatin.


  • 相关性
    Core 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. Subunit structure The nucleosome is a histone octamer containing two molecules each of H2A, H2B, H3 and H4 assembled in one H3-H4 heterotetramer and two H2A-H2B heterodimers. The octamer wraps approximately 147 bp of DNA. Post-translational modification Monoubiquitination at Lys-35 (H2BK34Ub) by the MSL1/MSL2 dimer is required for histone H3 'Lys-4' (H3K4me) and 'Lys-79' (H3K79me) methylation and transcription activation at specific gene loci, such as HOXA9 and MEIS1 loci. Similarly, monoubiquitination at Lys-121 (H2BK120Ub) by the RNF20/40 complex gives a specific tag for epigenetic transcriptional activation and is also prerequisite for histone H3 'Lys-4' and 'Lys-79' methylation. It also functions cooperatively with the FACT dimer to stimulate elongation by RNA polymerase II. H2BK120Ub also acts as a regulator of mRNA splicing: deubiquitination by USP49 is required for efficient cotranscriptional splicing of a large set of exons. Phosphorylation at Ser-37 (H2BS36ph) by AMPK in response to stress promotes transcription. Phosphorylated on Ser-15 (H2BS14ph) by STK4/MST1 during apoptosis; which facilitates apoptotic chromatin condensation. Also phosphorylated on Ser-15 in response to DNA double strand breaks (DSBs), and in correlation with somatic hypermutation and immunoglobulin class-switch recombination. GlcNAcylation at Ser-113 promotes monoubiquitination of Lys-121. It fluctuates in response to extracellular glucose, and associates with transcribed genes. Crotonylation (Kcr) is specifically present in male germ cells and marks testis-specific genes in post-meiotic cells, including X-linked genes that escape sex chromosome inactivation in haploid cells. Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors. It is also associated with post-meiotically activated genes on autosomes.
  • 细胞定位
  • 数据库链接
  • 别名
    • H2B K antibody
    • H2B type 12 antibody
    • H2B/b antibody
    • H2B/c antibody
    • H2B/d antibody
    • H2B/e antibody
    • H2B/f antibody
    • H2B/j antibody
    • H2B/n antibody
    • H2B/q antibody
    • H2B/r antibody
    • H2B/s antibody
    • HIRA-interacting protein 1 antibody
    • HIRA-interacting protein 2 antibody
    • Histone H2B type 1-B antibody
    • Histone H2B type 1-C/E/F/G/I antibody
    • Histone H2B type 1-D antibody
    • Histone H2B type 1-H antibody
    • Histone H2B type 1-J antibody
    • Histone H2B type 1-K antibody
    • Histone H2B type 1-L antibody
    • Histone H2B type 1-M antibody
    • Histone H2B type 1-N antibody
    • Histone H2B type 1-O antibody
    • Histone H2B type 2-E antibody
    • Histone H2B type 2-F antibody
    • Histone H2B type 3-B antibody
    • Histone H2B type F-S antibody
    • Histone H2B-GL105 antibody
    • Histone H2B.1 A antibody
    • Histone H2B.1 antibody
    • Histone H2B.1 B antibody
    • Histone H2B.2 antibody
    • Histone H2B.a antibody
    • Histone H2B.b antibody
    • Histone H2B.c antibody
    • Histone H2B.d antibody
    • Histone H2B.e antibody
    • Histone H2B.f antibody
    • Histone H2B.g antibody
    • Histone H2B.h antibody
    • Histone H2B.j antibody
    • Histone H2B.k antibody
    • Histone H2B.l antibody
    • Histone H2B.n antibody
    • Histone H2B.r antibody
    • Histone H2B.s antibody
    see all


  • Chromatin was prepared from Hela 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 ab12929 (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.

  • All lanes : Anti-Histone H2B (mono methyl K5) antibody - ChIP Grade (ab12929) at 1 µg/ml

    Lane 1 : Calf Thymus Histone Preparation Nuclear Lysate (ab121)
    Lane 2 : Calf Thymus Histone Preparation Nuclear Lysate (ab121) with Human Histone H2B (mono methyl K5) peptide (ab13211)
    Lane 3 : Calf Thymus Histone Preparation Nuclear Lysate (ab121) with Human Histone H2B peptide (ab13212)

    Lysates/proteins at 20 µg per lane.

    All lanes : IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilution

    Performed under reducing conditions.

    Predicted band size: 14 kDa

  • ab12929 at a 1/600 dilution for ChIP analysis of mouse dorsal skin epidermis whole tissue lysate, incubated for 15 hours at 4°C with ChIP dilution buffer. Cross-linking (X-ChIP) using 1% formaldehyde for 10 minutes.
    Detection step: Semiquantitative PCR.
    Negative control: Rabbit IgG.
    Cells untreated.

    See Abreview

  • Histone H2B (mono methyl K5) was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to Histone H2B (mono methyl K5) - ChIP Grade and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
    The antibody was incubated under agitation with Protein G beads for 10min, Hela whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
    Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70°C; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab12929.
    Secondary: Clean blot (HRP conjugate) at 1/1000 dilution.
    Band: 17kDa: Histone H2B (mono methyl K5).

  • ICC/IF image of ab12929 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 ab12929 at 1µg/ml overnight at +4°C. The secondary antibody (green) was a goat anti-rabbit DyLight® 488 (ab96899) 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.

  • IHC image of Histone H2B (mono methyl K5) staining in human pancreatic adenocarcinoma formalin fixed paraffin embedded tissue section, performed on a Leica Bond™ 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 ab12929, 0.1µg/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.


This product has been referenced in:
  • Majocchi S  et al. Epigenetic regulatory elements associate with specific histone modifications to prevent silencing of telomeric genes. Nucleic Acids Res N/A:N/A (2013). ChIP . Read more (PubMed: 24071586) »
  • Santoro SW & Dulac C The activity-dependent histone variant H2BE modulates the life span of olfactory neurons. elife 1:e00070 (2012). ICC/IF ; Mouse . Read more (PubMed: 23240083) »

See all 4 Publications for this product


Western blot
Loading amount
20 µg
Gel Running Conditions
Reduced Denaturing (15%)
Fruit fly (Drosophila melanogaster) Tissue lysate - nuclear (Fruit fly embryo (16hr))
Fruit fly embryo (16hr)
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 23°C

Abcam user community

Verified customer

提交于 Feb 09 2015

Western blot
Loading amount
20 µg
Gel Running Conditions
Reduced Denaturing (12.5%)
Rat Cell lysate - nuclear (PC12 cell line)
PC12 cell line
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 23°C

Abcam user community

Verified customer

提交于 Jan 08 2015

Blocking step
BSA as blocking agent for 20 minute(s) · Concentration: 3% · Temperature: 23°C
Human Cultured Cells (Human embryonic stem cells)
Human embryonic stem cells
Yes - 0.3% Triton X-100

Abcam user community

Verified customer

提交于 Jan 08 2014

Western blot
Loading amount
20 µg
Gel Running Conditions
Reduced Denaturing (15%)
Mouse Cell lysate - whole cell (Mouse embryonic fibroblasts)
Mouse embryonic fibroblasts
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 23°C

Abcam user community

Verified customer

提交于 Jan 08 2014

Thank you for contacting Abcam.

I am sorry that you are having problems with ab40886 in western blotting.

I would advise that you increase your primary antibody concentration to 1/500 and incubate at 4C overnight.

The anti...

Read More
Abcam guarantees this product to work in the species/application used in this Abreview.
Mouse Tissue lysate - whole (dorsal skin epidermis)
dorsal skin epidermis
Cross-linking (X-ChIP)
Duration of cross-linking step: 10 minute(s) and 0 second(s)
Specification of the cross-linking agent: 1% formaldehyde
Detection step
Semiquantitative PCR
Negative control
Rabbit IgG

Abcam user community

Verified customer

提交于 Feb 15 2010