ABE2853

Anti-Histone H3K27propionyl

• Synonym(s): H3K27propionyl
• UNSPSC Code: 12352203
• NACRES: NA.41

Properties

• biological source: rabbit
• Quality Level: 200
• antibody form: purified antibody
• antibody product type: primary antibodies
• mol wt: calculated mol wt 15.4 kDa; observed mol wt ~17 kDa
• purified by: affinity chromatography
• species reactivity: human, mouse
• packaging: antibody small pack of 100 μL
• technique(s): ChIP: suitable; dot blot: suitable; immunofluorescence: suitable; western blot: suitable
• isotype: IgG
• epitope sequence: N-terminal half
• Protein ID accession no.: NP_001363866
• UniProt accession no.: P68431
• storage temp.: 2-8°C

Description

Specificity

This rabbit polyclonal antibody specifically detects Histone H3 with propionylated lysine 27.

Immunogen

KLH-conjugated linear peptide corresponding to 10 amino acids surrounding propionylated lysine 27 of human Histone H3.

Application

Quality Control Testing

Evaluated by Western Blotting in lysates from HCT-116 cells treated with 10 mM Sodium propionate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected Histone H3 propionylated on lysine 27 in lysate from HCT-116 cells treated with 10 mM Sodium propionate.

Tested Applications

Chromatin Immunoprecipitation (ChIP) Analysis: 10 µg from a representative lot detected Histone H3K27propionyl in HCT-116 cells (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Dot Blot: A 1:2,000 dilution from a representative lot detected Histone H3K27propionyl peptide (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Western Blotting Analysis: A 1:5,000 dilution from a representative lot detected Histone H3K27propionyl in HCT-116 cells treated with 10 mM Sodium Propionate (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Immunofluorescence Analysis: A 1:500 dilution from a representative lot detected Histone H3K27propionyl in Mouse cecal sections (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user.

Target description

Histone H3 (UniProt: P68431; also known as Histone H3/a, Histone H3/b, Histone H3/c, Histone H3/d, Histone H3/f, Histone H3/h, Histone H3/I, Histone H3/j, Histone H3/k, Histone H3/l) is encoded by the HIST1H3A (also known as H3FA, HIST1H3B, H3FL, HIST1H3C, H3FC, HIST1H3D, H3FB, HISTH3F, H3FD, HIST1H3F, H3FI, HIST1H3G, H3FH, HIST1H3H, H3FK, HIST1H3I, H3FF, HIST1H3J, H3FJ) gene (Gene ID: 8350, 8351, 8352, 8354, 8355, 8356, 8357, 8358, 8968) in human. Histones and DNA assemble to form nucleosomes and each nucleosome organizes a stretch of DNA wrapped around a histone octamer that is composed of a central (H3-H4)2 tetramer, flanked by two H2A-H2B dimers. A large number of variants of Histone H3 have been described in mammals. The two main variants, H3.1 and H3.3, show different genomic localization patterns in animals. They possess distinct histone chaperones, CAF-1 and HIRA, which play important role in mediating DNA-synthesis-dependent and -independent nucleosome assembly. Histone H3.1 serves as the canonical histone, which is incorporated during DNA replication, whereas H3.3 acts as the replacement histone that can be incorporated outside of S-phase during chromatin-disrupting processes like transcription. Histone H3 features a main globular domain and a long N-terminal tail, which protrudes from the globular nucleosome core and can undergo several different types of epigenetic modifications that influence cellular processes. The amino-terminal tails of histone proteins are subject to several posttranslational modifications, including acetylation, methylation, and phosphorylation, which recruit downstream regulatory factors, influence chromatin structure, and are critical determinants of transcription. These modifications on histones, known as histone acyl marks, are involved in transcription regulation. However, the exact role of other modifications, such as propionylation and butyrlation are still under investigation. These modifications are detected at comparable levels to acetylation on selected residues in histone H3. (Ref.: Scott, WA., and Campos, EI. (2020). Front. Cell Dev. Biol. 8; 701; Allis CD., and Jenuwein, T. (20160. Nat. Rev. Genet. 17(8); 487-500).

Physical form

Purified rabbit polyclonal antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Reconstitution

0.5 mg/mL. Please refer to guidance on suggested starting dilutions and/or titers per application and sample type.

Storage and Stability

Recommended storage: +2°C to +8°C.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Safety Information

• Storage Class Code: 12 - Non Combustible Liquids
• WGK: WGK 1
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable