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Histone H4K16ac antibody (mAb) (Clone MABI 0416)

Host / Isotype

Mouse / IgG1

Reactivity

Human, Wide Range Predicted

Applications

ChIP, DB, IF, WB

CloneNo.

MABI 0416

Cat No : 61529 61529

Synonyms

histone H4, h4k16ac, histone, H4, histone-H4, histoneH4, mAb, monoclonal, mabi, H4 AcK16, Histone H4 Acetyl Lys16, Histone H4 Acetyl K16, Histone H4 Ac Lys16, H4 Acetyl Lys16, H4 Acetyl K16, H4 Ac Lys16, Histone H4 Acetylated Lysine 16, Histone H4 Acetyl Lysine16, H4 Acetylated Lysine 16, H4 Acetyl Lysine16, antibody, antibodies, acetyl, Histone H4, histone acetylation, nucleosome, chromatin, antibody, antibodies, chromatin immunoprecipitation, chip, western blotting, wb

验证数据展示

  • Histone H4K16ac antibody (mAb) tested by ChIP analysis. Chromatin IP performed using the ChIP-IT Express Kit (Catalog No. 53008) and HeLa Chromatin (1.5 x 106 cell equivalents per ChIP) using 3 ug of Histone H4K16ac (mAb) or the equivalent amount of mouse IgG as a negative control. Real time, quantitative PCR (RT-qPCR) was performed on DNA purified from each of the ChIP reactions using a primer pair specific for the PABPC1 gene. Data are presented as Fold Enrichment of the ChIP antibody signal versus the negative control IgG using the ddCT method.

    Histone H4K16ac antibody (mAb) tested by ChIP analysis. Chromatin IP performed using the ChIP-IT Express Kit (Catalog No. 53008) and HeLa Chromatin (1.5 x 106 cell equivalents per ChIP) using 3 ug of Histone H4K16ac (mAb) or the equivalent amount of mouse IgG as a negative control. Real time, quantitative PCR (RT-qPCR) was performed on DNA purified from each of the ChIP reactions using a primer pair specific for the PABPC1 gene. Data are presented as Fold Enrichment of the ChIP antibody signal versus the negative control IgG using the ddCT method.

  • Histone H4K16ac antibody (mAb) tested by Western blot. HeLa nuclear extract (20 ug per lane) probed with Histone H4K16ac (mAb) at a 2 ug/ml dilution. Lane 1: No treatment. Lane 2: cells treated with sodium butyrate.

    Histone H4K16ac antibody (mAb) tested by Western blot. HeLa nuclear extract (20 ug per lane) probed with Histone H4K16ac (mAb) at a 2 ug/ml dilution. Lane 1: No treatment. Lane 2: cells treated with sodium butyrate.

  • Histone H4K16ac antibody (mAb) specificity tested by peptide array analysis. Peptide array analysis was used to confirm the specificity of this antibody for its intended modification. Histone H4K16ac antibody (mAb) was applied at a dilution of 0.7 ug/ml to Active Motif's MODified Histone Peptide Array (Catalog No. 13001). The arrays were scanned with ArrayAnalysis Software 7 and the results plotted. Specificity data is shown for the most reactive peptides and those related to the immunogen.

    Histone H4K16ac antibody (mAb) specificity tested by peptide array analysis. Peptide array analysis was used to confirm the specificity of this antibody for its intended modification. Histone H4K16ac antibody (mAb) was applied at a dilution of 0.7 ug/ml to Active Motif's MODified Histone Peptide Array (Catalog No. 13001). The arrays were scanned with ArrayAnalysis Software 7 and the results plotted. Specificity data is shown for the most reactive peptides and those related to the immunogen.

  • Histone H4K16ac antibody (mAb) tested by dot blot analysis. Dot blot analysis was used to confirm the specificity of Histone H4K16ac antibody (mAb) for acetyl-Lys16 histone H4. Acetylated peptides corresponding to the immunogen and related peptides were spotted onto PVDF and probed with Histone H4K16ac antibody (mAb) at a dilution of 2 ug/ml. The amount of peptide (picomoles) spotted is indicated next to each row. Lane 1: acetyl-Lys5 peptide. Lane 2: unmodified Lys5 peptide. Lane 3: acetyl-Lys8 peptide. Lane 4: unmodified Lys8 peptide. Lane 5: acetyl-Lys12 peptide. Lane 6: unmodified Lys12 peptide. Lane 7: acetyl-Lys16 peptide. Lane 8: unmodified Lys16 peptide. Lane 9: acetyl-Lys20 peptide. Lane 10: unmodified Lys20 peptide. Lane 11: acetyl-Lys31 peptide. Lane 12: unmodified Lys31 peptide.

    Histone H4K16ac antibody (mAb) tested by dot blot analysis. Dot blot analysis was used to confirm the specificity of Histone H4K16ac antibody (mAb) for acetyl-Lys16 histone H4. Acetylated peptides corresponding to the immunogen and related peptides were spotted onto PVDF and probed with Histone H4K16ac antibody (mAb) at a dilution of 2 ug/ml. The amount of peptide (picomoles) spotted is indicated next to each row. Lane 1: acetyl-Lys5 peptide. Lane 2: unmodified Lys5 peptide. Lane 3: acetyl-Lys8 peptide. Lane 4: unmodified Lys8 peptide. Lane 5: acetyl-Lys12 peptide. Lane 6: unmodified Lys12 peptide. Lane 7: acetyl-Lys16 peptide. Lane 8: unmodified Lys16 peptide. Lane 9: acetyl-Lys20 peptide. Lane 10: unmodified Lys20 peptide. Lane 11: acetyl-Lys31 peptide. Lane 12: unmodified Lys31 peptide.

产品信息

Tested Applications ChIP, DB, IF, WB

Applications Validated by Active Motif: ChIP: 2 - 5 ug per ChIP WB*: 0.5 - 2 ug/ml dilution *Note: many chromatin-bound proteins are not soluble in a low salt nuclear extract and fractionate to the pellet. Therefore, we recommend a High Salt / Sonication Protocol when preparing nuclear extracts for Western Blot.
Tested Reactivity Human, Wide Range Predicted
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
ModificationAcetylated
Immunogen This antibody was raised against a synthetic peptide containing acetyl-lysine 16 of human Histone H4.
Full Name Histone H4K16ac antibody (mAb) (Clone MABI 0416)
Synonyms histone H4, h4k16ac, histone, H4, histone-H4, histoneH4, mAb, monoclonal, mabi, H4 AcK16, Histone H4 Acetyl Lys16, Histone H4 Acetyl K16, Histone H4 Ac Lys16, H4 Acetyl Lys16, H4 Acetyl K16, H4 Ac Lys16, Histone H4 Acetylated Lysine 16, Histone H4 Acetyl Lysine16, H4 Acetylated Lysine 16, H4 Acetyl Lysine16, antibody, antibodies, acetyl, Histone H4, histone acetylation, nucleosome, chromatin, antibody, antibodies, chromatin immunoprecipitation, chip, western blotting, wb
Molecular weight 8 kDa
GenBank accession numberNP_778224
RRIDAB_2793671
Purification Method Protein G Chromatography
Buffer PBS pH 7.5 containing 30% glycerol, 0.3 M NaCl, and 0.035% sodium azide. Sodium azide is highly toxic.
Storage Some products may be shipped at room temperature. This will not affect their stability or performance. Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions for storage at -20°C for up to 2 years. Keep all reagents on ice when not in storage.

背景介绍

Histone H4 is one of the core components of the nucleosome. The nucleosome is the smallest subunit of chromatin and consists of 147 base pairs of DNA wrapped around an octamer of core histone proteins (two each of Histone H2A, Histone H2B, Histone H3 and Histone H4). Histone H1 is a linker histone, present at the interface between the nucleosome core and DNA entry/exit points; it is responsible for establishing higher-order chromatin structure. Chromatin is subject to a variety of chemical modifications, including post-translational modifications of the histone proteins and the methylation of cytosine residues in the DNA. Reported histone modifications include acetylation, methylation, phosphorylation, ubiquitylation, glycosylation, ADP-ribosylation, carbonylation and SUMOylation; they play a major role in regulating gene expression. Lysine N-e-acetylation is a dynamic, reversible and tightly regulated protein and histone modification that plays a major role in chromatin remodeling and in the regulation of gene expression in various cellular functions. NoRC is a SMARCA5 (SNF2h)-containing chromatin remodeling complex. The bromodomain of TIP5, the large subunit of NoRC, interacts with acetylated Histone H4 Lys16, (H4K16ac) and cooperates with an adjacent PHD finger to recruit histone deacetylases and DNA methyltransferases to rDNA, leading to the silencing of rDNA.