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ABE1447

Sigma-Aldrich

Anti-Histone H3 Antibody, K36M mutant

from rabbit, purified by affinity chromatography

Synonyme(s) :

H3K36M, Histone H3 K36M mutant, H3 histone family, member T, K36M mutant, Histone cluster 3, K36M mutant

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

primary antibodies

Clone

polyclonal

Produit purifié par

affinity chromatography

Espèces réactives

mouse, human

Réactivité de l'espèce (prédite par homologie)

bovine (based on 100% sequence homology), rabbit (based on 100% sequence homology), rat (based on 100% sequence homology), porcine (based on 100% sequence homology)

Technique(s)

dot blot: suitable
immunohistochemistry: suitable
western blot: suitable

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

ambient

Modification post-traductionnelle de la cible

mutation (Lys36Met)

Informations sur le gène

human ... HIST1H3F(8968)

Description générale

Histone H3 is one of the five main histone proteins involved in the structure of chromatin in eukaryotic cells. Featuring a main globular domain and a long N-terminal tail, H3 is involved with the structure of the nucleosomes of the ′beads on a string′ structure. The N-terminal tail of histone H3 protrudes from the globular nucleosome core and can undergo several different types of epigenetic modifications that influence cellular processes. These modifications include the covalent attachment of methyl or acetyl groups to lysine and arginine amino acids and the phosphorylation of serine or threonine. Histone H3 variants (H3.1, H3.2 and H3.3) have been implicated in the epigenetic memory of cellular state. Genome-wide patterns of H3 are dependent on amino acid sequence and change with cellular differentiation at developmentally regulated loci. Somatic missense mutations in histone H3 genes are found in several pediatric brain and bone malignancies, among which ~90% of the chondroblastomas are identified with histone H3 K36M mutation (H3K36M). Loss of H3K36 methylation due to H3K36M mutation causes a genome-wide upregulation of H3K27 methylation, leading to an altered polycomb repressive complex 1 (PRC1) distribution and re-activation of PRC1-suppressed target genes involved in mesenchymal differentiatio

Spécificité

Predicted to react with a broad-range of species based on 100% sequence homology.
This rabbit polyclonal antibody specifically detects histone H3 K36M mutation (H3K36M) without cross-reactivity toward histone H3 without H3K36M mutation.

Immunogène

KLH-conjugated linear peptide corresponding to the target region sequence with K36M mutation.

Application

Anti-Histone H3, K36M mutant, Cat. No. ABE1447, is a highly specific rabbit polyclonal antibody that targets Histone H3 K36M mutation (H3K36M) and has been tested in Dot Blot, Immunohistochemistry, and Western Blotting.
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot immunostained paraffin-embedded sections from human chondroblastoma tissues carrying histone H3 K36M mutation (Courtesy of Denise Bechet and Nada Jabado from McGill University, Montreal, Quebec, Canada).

Dot Blot Analysis: A representative lot detected histone H3 peptide representing epitope region sequence with K36M mutation (H3K36M), but not peptides representing wild-type sequence with either unmodified methylated K36 residue (Lu, C., et al. (2016). Science. 352(6287):844-849).

Immunohistochemistry Analysis: A representative lot immunostained paraffin-embedded sections from human soft tissue undifferentiated sarcoma carrying H3.1K36M mutation (Lu, C., et al. (2016). Science. 352(6287):844-849).

Immunohistochemistry Analysis: A representative lot immunostained paraffin-embedded H3.3K36M mutant tumors from mice xenografts (Lu, C., et al. (2016). Science. 352(6287):844-849).

Immunohistochemistry Analysis: A representative lot immunostained paraffin-embedded sections from human chondroblastoma tissues carrying histone H3 K36M mutation (Lu, C., et al. (2016). Science. 352(6287):844-849).

Western Blotting Analysis: A representative lot detected a target band in histone acid extracts from murine mesenchymal progenitor cells expresssing K36M mutant, but not wild-type, histone H3.3 (Lu, C., et al. (2016). Science. 352(6287):844-849).

Western Blotting Analysis: A representative lot detected a target band in histone acid extracts from human chondroblastoma samples with H3K36M mutation, but not in human chondrocarcinoma samples H3K36M mutation(Lu, C., et al. (2016). Science. 352(6287):844-849).
Research Category
Epigenetics & Nuclear Function

Qualité

Evaluated by Western Blotting of H3K36M overexpression in HEK293 transfectants.

Western Blotting Analysis: A 1:250 dilution of this antibody detected overexpressed K36M mutant, but not wild-type, human histone H3.3 in 10 µg of lysate from HEK293 transfectants.

Description de la cible

~17 kDa observed. Uncharacterized bands may be observed in some lysate(s).

Forme physique

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

Stockage et stabilité

Stable for 1 year at 2-8°C from date of receipt.

Autres remarques

Concentration: Please refer to lot specific datasheet.

Clause de non-responsabilité

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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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Haoran Mu et al.
Orthopaedic surgery, 13(2), 616-622 (2021-02-24)
Whether H3.3 K36M mutation (H3K36M) could be an approach if the diagnosis of chondroblastoma (CB) patients was indistinct and it was suspected to be unclear clinically. We reviewed and compared our clinical experiences of CB cases and some suspected cases
Salina Yuan et al.
Cancer discovery, 10(6), 854-871 (2020-03-20)
Epithelial plasticity, reversible modulation of a cell's epithelial and mesenchymal features, is associated with tumor metastasis and chemoresistance, leading causes of cancer mortality. Although different master transcription factors and epigenetic modifiers have been implicated in this process in various contexts

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