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ABE2852

Anti-Histone H3K9propionyl

Synonym(e):

H3K9propionyl

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NACRES:
NA.74
UNSPSC Code:
12352203
Species reactivity:
mouse, human
Technique(s):
ChIP: suitable, dot blot: suitable, immunofluorescence: suitable, western blot: suitable
Application:
ChIP, DB, IF, WB
Citations:
-
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biological source

rabbit

Quality Segment

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

mouse, human

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

Protein ID accession no.

UniProt accession no.

storage temp.

2-8°C

General 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).

Immunogen

KLH-conjugated linear peptide corresponding to 10 amino acids surrounding propionylated lysine 9 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 9 in lysate from HCT-116 cells treated with 10 mM Sodium propionate.

Tested Applications

Western Blotting Analysis: A 1:20,000 dilution from a representative lot detected Histone H3K9propionyl in HCT-116 cell lysate treated with Sodium Propionate (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Chromatin Immunoprecipitation (ChIP) Analysis: 10 µg from a representative lot detected Histone H3K9propionyl in HCT-116 cells (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 H3K9propionyl in Mouse intestine (Data courtesy of Dr. Leah Gates, Dave Allis Lab @ Rockefeller University, New York).

Dot Blot: A 1:20,000 dilution from a representative lot detected Histone H3K9propionyl peptide (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.

Biochem/physiol Actions

This rabbit polyclonal antibody specifically detects Histone H3 with propionylated lysine 9.

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.

Preparation Note

Recommended storage: +2°C to +8°C.
Reconstitute lyophilized antibody pellet with 25μL of ultrapure water or Phosphate Buffered Saline (PBS). Please refer to our reconstitution protocol and the specific application guidance on the suggested starting dilutions and sample type.

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.

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Dieser Artikel
ABE2853ABE2854SAB5701101
description

-

description

-

description

-

description

-

antibody form

purified antibody

antibody form

purified antibody

antibody form

purified antibody

antibody form

-

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

species reactivity

mouse, human

species reactivity

human, mouse

species reactivity

human, mouse

species reactivity

-

mol wt

calculated mol wt 15.4 kDa, observed mol wt ~17 kDa

mol wt

observed mol wt ~17 kDa, calculated mol wt 15.4 kDa

mol wt

observed mol wt ~17 kDa, calculated mol wt 15.4 kDa

mol wt

-

technique(s)

immunofluorescence: suitable, dot blot: suitable, western blot: suitable, ChIP: suitable

technique(s)

dot blot: suitable, immunofluorescence: suitable, western blot: suitable, ChIP: suitable

technique(s)

-

technique(s)

western blot: 1:500-1:2000

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C


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