Anti-NF-kB p65 (acetyl K310)抗体- ChIP Grade (ab19870)

概述

  • 产品名称Anti-NF-kB p65 (acetyl K310)抗体- ChIP Grade
    参阅全部 NF-kB p65 一抗
  • 描述
    兔多克隆抗体to NF-kB p65 (acetyl K310) - ChIP Grade
  • 经测试应用适用于: WB, IP, Dot blot, ICC, ChIPmore details
  • 种属反应性
    与反应: Mouse, Rat, Human
  • 免疫原

    Synthetic peptide corresponding to Human NF-kB p65 aa 300-400 (internal sequence) conjugated to Keyhole Limpet Haemocyanin (KLH).
    (Peptide available as ab20612)

  • 阳性对照
    • This antibody gave a positive signal in Rat lung tissue lysate.

应用

Our Abpromise guarantee covers the use of ab19870 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
WB Use a concentration of 2.5 µg/ml. Detects a band of approximately 65 kDa (predicted molecular weight: 65 kDa). Collaborator data suggests that immunoprecipitation of this antibody prior to Western blotting is required to obtain the best results (see images)
IP Use a concentration of 2.5 µg/ml.
Dot blot Use at an assay dependent dilution.
ICC Use at an assay dependent dilution. In ICC/IF ab19870 recognizes various acetylated nuclear protein(s), as the signal is also observed in control cells; the signal in ICC is HDACi-dependent.
ChIP Use at an assay dependent concentration. PubMed: 22249179

靶标

  • 功能NF-kappa-B is a pleiotropic transcription factor which is present in almost all cell types and is involved in many biological processed such as inflammation, immunity, differentiation, cell growth, tumorigenesis and apoptosis. NF-kappa-B is a homo- or heterodimeric complex formed by the Rel-like domain-containing proteins RELA/p65, RELB, NFKB1/p105, NFKB1/p50, REL and NFKB2/p52 and the heterodimeric p65-p50 complex appears to be most abundant one. The dimers bind at kappa-B sites in the DNA of their target genes and the individual dimers have distinct preferences for different kappa-B sites that they can bind with distinguishable affinity and specificity. Different dimer combinations act as transcriptional activators or repressors, respectively. NF-kappa-B is controlled by various mechanisms of post-translational modification and subcellular compartmentalization as well as by interactions with other cofactors or corepressors. NF-kappa-B complexes are held in the cytoplasm in an inactive state complexed with members of the NF-kappa-B inhibitor (I-kappa-B) family. In a conventional activation pathway, I-kappa-B is phosphorylated by I-kappa-B kinases (IKKs) in response to different activators, subsequently degraded thus liberating the active NF-kappa-B complex which translocates to the nucleus. NF-kappa-B heterodimeric p65-p50 and p65-c-Rel complexes are transcriptional activators. The NF-kappa-B p65-p65 complex appears to be involved in invasin-mediated activation of IL-8 expression. The inhibitory effect of I-kappa-B upon NF-kappa-B the cytoplasm is exerted primarily through the interaction with p65. p65 shows a weak DNA-binding site which could contribute directly to DNA binding in the NF-kappa-B complex. Associates with chromatin at the NF-kappa-B promoter region via association with DDX1.
  • 序列相似性Contains 1 RHD (Rel-like) domain.
  • 结构域the 9aaTAD motif is a transactivation domain present in a large number of yeast and animal transcription factors.
  • 翻译后修饰Ubiquitinated, leading to its proteasomal degradation. Degradation is required for termination of NF-kappa-B response.
    Monomethylated at Lys-310 by SETD6. Monomethylation at Lys-310 is recognized by the ANK repeats of EHMT1 and promotes the formation of repressed chromatin at target genes, leading to down-regulation of NF-kappa-B transcription factor activity. Phosphorylation at Ser-311 disrupts the interaction with EHMT1 without preventing monomethylation at Lys-310 and relieves the repression of target genes.
    Phosphorylation at Ser-311 disrupts the interaction with EHMT1 and promotes transcription factor activity (By similarity). Phosphorylation on Ser-536 stimulates acetylation on Lys-310 and interaction with CBP; the phosphorylated and acetylated forms show enhanced transcriptional activity.
    Reversibly acetylated; the acetylation seems to be mediated by CBP, the deacetylation by HDAC3. Acetylation at Lys-122 enhances DNA binding and impairs association with NFKBIA. Acetylation at Lys-310 is required for full transcriptional activity in the absence of effects on DNA binding and NFKBIA association. Acetylation can also lower DNA-binding and results in nuclear export. Interaction with BRMS1 promotes deacetylation of 'Lys-310'.
  • 细胞定位Nucleus. Cytoplasm. Nuclear, but also found in the cytoplasm in an inactive form complexed to an inhibitor (I-kappa-B). Colocalized with RELA in the nucleus upon TNF-alpha induction.
  • Information by UniProt
  • 数据库链接
  • 别名
    • Avian reticuloendotheliosis viral (v rel) oncogene homolog A antibody
    • MGC131774 antibody
    • NF kappa B p65delta3 antibody
    • NFKB3 antibody
    • Nuclear Factor NF Kappa B p65 Subunit antibody
    • Nuclear factor NF-kappa-B p65 subunit antibody
    • Nuclear factor of kappa light polypeptide gene enhancer in B cells 3 antibody
    • Nuclear factor of kappa light polypeptide gene enhancer in B-cells 3 antibody
    • OTTHUMP00000233473 antibody
    • OTTHUMP00000233474 antibody
    • OTTHUMP00000233475 antibody
    • OTTHUMP00000233476 antibody
    • OTTHUMP00000233900 antibody
    • p65 antibody
    • p65 NF kappaB antibody
    • p65 NFkB antibody
    • relA antibody
    • TF65_HUMAN antibody
    • Transcription factor p65 antibody
    • v rel avian reticuloendotheliosis viral oncogene homolog A (nuclear factor of kappa light polypeptide gene enhancer in B cells 3 (p65)) antibody
    • V rel avian reticuloendotheliosis viral oncogene homolog A antibody
    • v rel reticuloendotheliosis viral oncogene homolog A (avian) antibody
    • V rel reticuloendotheliosis viral oncogene homolog A, nuclear factor of kappa light polypeptide gene enhancer in B cells 3, p65 antibody
    see all

Anti-NF-kB p65 (acetyl K310) antibody - ChIP Grade 图像

  • All lanes : Anti-NF-kB p65 (acetyl K310) antibody - ChIP Grade (ab19870) at 1/1000 dilution

    Lane 1 : HCT116 whole cell lysate treated with DMSO for 24 hrs (control)
    Lane 2 : HCT116 whole cell lysate treated with 2 µM SAHA for 24 hrs
    Lane 3 : MEF whole cell lysate treated with DMSO for 24 hrs (control)
    Lane 4 : MEF whole cell lysate treated with 2 µM SAHA for 24 hrs

    Lysates/proteins at 60 µg per lane.

    Secondary
    Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/10000 dilution
    Developed using the ECL technique

    Performed under reducing conditions.

    Predicted band size : 65 kDa
    Observed band size : 65 kDa
    Additional bands at : 140 kDa (possible non-specific binding),15 kDa (possible non-specific binding),40 kDa (possible non-specific binding),45 kDa (possible non-specific binding),90 kDa (possible non-specific binding).

    Exposure time : 2 minutes

    This image is courtesy of an Abreview submitted by Christian Marx

    See Abreview

  • ab19870 staining NF-kB p65 (acetyl K310) in Mouse bladder tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with paraformaldehyde and blocked with 10% HIHS for 90 minutes at 20°C; antigen retrieval was by heat mediation in a citrate buffer. Samples were incubated with primary antibody (1/300 in in 0.3% PBS Triton with 1% HIHS) for 24 hours at 4°C. A Cy3® conjugated Donkey anti mouse IgG polyclonal (1/250) was used as the secondary antibody.

    See Abreview

  • Rabbit polyclonal to NF-kB p65 (acetyl K310) (ab19870; 2.5µg/ml) in 1% non-fat milk TBS-T incubated for 3h at room temperature. Exposure time: 75 min normal ECL. This Dot blot demonstrates that ab19870 recognized upto 10ng of purified peptide on a PVDF membrane.

  • Western Blot with ab19870 after p65 Immunoprecipitation: rabbit polyclonal to NF-kB p65 (acetyl K310) (ab19870; 2.5µg/ml) in 1% non-fat milk TBS-T incubated for 3 hours at room temperature. Exposure time: 1 min normal ECL. Tested samples: nuclear extracts (180 µg) of immortalized p65-/- mouse cells, complemented with the empty vector (pRRL), wild-type p65 (Wt) and non-acetylatable K310 (K310R). The samples tested were treated with deacetylase inhibitors HDACi (TSA + Nicotinamide) and TNF-alpha. The samples were immunoprecipitated with 2µg of alpha-p65 and subsequently analysed by Western blot with Rabbit polyclonal to NF-kB p65 (acetyl K310) (ab19870). Predicted band size = 65kDa, Observed band size = 75kDa. The p65 band runs higher in this SDS-PAGE blot as it contains a myc-tag.

    All lanes : Anti-NF-kB p65 (acetyl K310) antibody - ChIP Grade (ab19870) at 2.5 µg/ml

    Lane 1 : pRRL untreated
    Lane 2 : pRRL HDACi
    Lane 3 : pRRL HDACi + TNF
    Lane 4 : Wt untreated
    Lane 5 : Wt HDACi
    Lane 6 : Wt HDACi + phorbol myristate acetate
    Lane 7 : K310R untreated
    Lane 8 : K310R HDACi
    Lane 9 : K310R HDACi + phorbol myristate acetate

    Lysates/proteins at 75 µg per lane.

    Developed using the ECL technique

    Predicted band size : 65 kDa
    Observed band size : 75 kDa (why is the actual band size different from the predicted?)


    Exposure time : 1 hour

    This image is courtesy of Christine Buerki and Karin Rothgiesser, University of Zurich, Switzerland

    ab19870 recognizes Rabbit polyclonal to NF-kB p65 (acetyl K310) specifically at ~75kDa (indicated by the arrow) is this SDS-PAGE blot. The p65 band runs higher than 65kDa in this SDS-PAGE blot as it contains a myc-tag. We are sure that the band at ~75kDa is p65 since p65 specific antibodies detect the same band in IP and WB and there is no signal in the p65 knock-out cell line with ab19870. A number of additonal bands are recognized by ab19870 when tested with endogenous p65 from whole cell extracts, we do not know the identity of these bands.

    Tested samples: nuclear extracts (75µg) of immortalized p65-/- mouse cells, complemented with the empty ve

  • Anti-NF-kB p65 (acetyl K310) antibody - ChIP Grade (ab19870) at 1 µg/ml + Lung (Rat) Tissue Lysate at 10 µg

    Secondary
    Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (ab97080) at 1/5000 dilution

    Performed under reducing conditions.

    Predicted band size : 65 kDa
    Observed band size : 72 kDa (why is the actual band size different from the predicted?)
    Additional bands at : 15 kDa. We are unsure as to the identity of these extra bands.

    Exposure time : 4 minutes

Anti-NF-kB p65 (acetyl K310) antibody - ChIP Grade (ab19870)参考文献

This product has been referenced in:
  • Ma M  et al. MiR-487a Promotes TGF-ß1-induced EMT, the Migration and Invasion of Breast Cancer Cells by Directly Targeting MAGI2. Int J Biol Sci 12:397-408 (2016). WB ; Human . Read more (PubMed: 27019625) »
  • Wang X  et al. Resveratrol attenuates microvascular inflammation in sepsis via SIRT-1-Induced modulation of adhesion molecules in ob/ob mice. Obesity (Silver Spring) 23:1209-17 (2015). WB ; Human . Read more (PubMed: 25959124) »

See all 22 Publications for this product

Product Wall

Application Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample Mouse Tissue sections (Bladder)
Antigen retrieval step Heat mediated - Buffer/Enzyme Used: PH6 Citrate Buffer
Permeabilization No
Specification Bladder
Blocking step HIHS as blocking agent for 1 hour(s) and 30 minute(s) · Concentration: 10% · Temperature: 20°C
Fixative Paraformaldehyde
Username

Mr. Spenser Souza

Verified customer

提交于 May 12 2016

Application Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample Mouse Tissue sections (Testis)
Antigen retrieval step Heat mediated - Buffer/Enzyme Used: Citrate buffer ph6 20 min at 97ºC in a PT link
Permeabilization No
Specification Testis
Blocking step Serum as blocking agent for 30 minute(s) · Concentration: 10% · Temperature: 25°C
Fixative Formaldehyde
Username

Abcam user community

Verified customer

提交于 Sep 24 2015

Abcam guarantees this product to work in the species/application used in this Abreview.
Application Western blot
Loading amount 100000 cells
Gel Running Conditions Reduced Denaturing (12 %)
Sample Human Cell lysate - whole cell (breast)
Specification breast
Blocking step Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Username

Abcam user community

Verified customer

提交于 Aug 20 2013

Abcam guarantees this product to work in the species/application used in this Abreview.
Application Western blot
Sample Human Cell lysate - whole cell (HCT116 colon cancer cell line and MEF cell line)
Loading amount 60 µg
Specification HCT116 colon cancer cell line and MEF cell line
Treatment DMSO control and 2 µM SAHA for 24 hrs
Gel Running Conditions Reduced Denaturing (13%)
Blocking step Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Username

Mr. Christian Marx

Verified customer

提交于 Feb 11 2013

Thank you for your email. I am sorry to hear that you have been experiencing problems with this antibody.

I have read the details you have kindly provided and have following further questions for better understanding of the problem;

-...

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Thank you for your reply.

I have arranged a free of charge vial of ab52175 to ship out to Cedarlane on their next order from us as a replacement for the faulty ab19870 that you ordered through them on reference number is 389794. When they get...

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Thank you for your reply and for clarifying those additional protocol details.

I may be able to look up your order details for you if you can provide more information. What institution are you working in? Did you order through a distributor? ...

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Thank you very much for your interest in ab19870.

To our knowledge,ab19870 has not been tested in IHC-P. Therefore, I can offer a discount off a future purchase if you buyab19870 now, test it inIHC-P and submit feedback to us in the form of ...

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