Anti-Histone [F152C25W] Universal Antibody

This mouse IgG2a monoclonal antibody [F152C25W] was generated from an autoimmune mouse model and recognizes bovine, hamster, human, mouse and marsupial histones (all classes; H1 and core histones).


  • Reacts with bovine, hamster, human, mouse and marsupial histones assayed (all classes; H1 and core histones)
  • Suitable for Western Blot, ELISA and Immunofluorescence applications

Histones are the chief organizing proteins of DNA in the nucleus of all eukaryotic cells. They can be grouped into five major classes, whereof four form a nucleosome core particle that DNA is wrapped around, and the fifth organizes the linker DNA between the nucleosomes. Histones are among the most highly conserved proteins between species, which underscores their essential function for life of eukaryotic cells.

From the laboratory of Kim S. Wise, PhD, University of Missouri - Columbia.

The Investigator's Annexe Part of The Investigator's Annexe program.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
Anti-Histone [F152C25W] Universal Antibody
100ug In stock
Regular Price:$321.00
On Sale:

Product Type: Antibody
Antigen: Histones (all classes; H1 and core histones)
Molecular Weight: Various, per known histone species
Isotype: IgG2a
Clonality: Monoclonal
Clone Name: F152C25W
Reactivity: All vertebrate species assayed: bovine, hamster, human, mouse and marsupial
Immunogen: Naturally occurring autoantibody
Species Immunized: Mouse
Purification Method: Protein G
Buffer: 0.1M Sodium Phosphate, pH 7.4, 0.15M NaCl, 0.05% (w/v) Sodium Azide
Tested Applications: WB (1:1000), IF (1:1000 ), ELISA
Storage: -20C
Shipped: Cold packs


Western Blot

(Panel A) Proteins separated by SDS-PAGE (Laemmli system, 10-18% linear gradient) were stained with Coomassie Blue. Samples include:standard mol wt markers (lane 1), expressed in kilodaltons at left; histone mixture (lane 2); histone H1 (lane 3); histone H2B (lane 4), and histone H4 (lane 5). Fractionated or purified histones from calf thymus were obtained from Boehringer Mannheim Biochemicals. (Panel B) Western immunoblot of proteins separated by SDS-PAGE and stained with mAb F152C25W. Blots were generated from a separate gel (run under the same conditions as in panel A) containing 5 ug per well of: histone H1 (lane 1); histone H2B (lane 2); histone H4 (lane 3), and histone mixture (lane 4). The positions of the various histones are indicated.

Procedure adapted from: Hardin, JA. et al., Proc. Natl. Acad. Sci. USA 80:7410-7414.

Immunofluorescence Microscopy

Fibroblast monolayers were fixed in cold methanol and incubated with mAb followed by FITC-conjugated goat anti-mouse Ig secondary Ab. (Bars = 10 microns). (Panel A): Incubated with mAb F152C25W; shows smooth, intense, specific nuclear staining. (Panel B): Incubated with irrelevant mAb of different specificity; to emphasize unstained nuclei.

From the laboratory of Kim S. Wise, PhD, University of Missouri - Columbia.

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