07-540
Anti-acetyl-Histone H3 (Lys36) Antibody
serum, Upstate®
Synonyme(s) :
H3K36Ac, Histone H3 (acetyl K36)
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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
serum
Type de produit anticorps
primary antibodies
Clone
polyclonal
Espèces réactives
human
Fabricant/nom de marque
Upstate®
Technique(s)
multiplexing: suitable
western blot: suitable
Numéro d'accès NCBI
Numéro d'accès UniProt
Conditions d'expédition
wet ice
Modification post-traductionnelle de la cible
acetylation (Lys36)
Informations sur le gène
human ... H3F3B(3021)
Spécificité
Broad species cross reactivity is expected
Recognizes Histone H3 when acetylated on Lys36
Immunogène
KLH-conjugated, synthetic peptide containing the sequence ...GV[AcK]KP... in which [AcK] corresponds to acetyl-lysine 36 of human histone H3.
Application
Suggested dilutions:
Western Blot: 1:5000 - 1:20,000
ChIP Analysis: A representative lot was used by an independent laboratory for ChIP (Gatta, R., et al. (2011). Epigenetics. 6(4):526-534.)
Western Blot: 1:5000 - 1:20,000
ChIP Analysis: A representative lot was used by an independent laboratory for ChIP (Gatta, R., et al. (2011). Epigenetics. 6(4):526-534.)
Research Category
Epigenetics & Nuclear Function
Epigenetics & Nuclear Function
Research Sub Category
Histones
Histones
Use Anti-acetyl-Histone H3 (Lys36) Antibody (Rabbit Polyclonal Antibody) validated in WB, Mplex to detect acetyl-Histone H3 (Lys36) also known as H3K36Ac, Histone H3 (acetyl K36).
Qualité
Routinely evaluated by immunoblot.
Description de la cible
~17kDa
Forme physique
100μl of rabbit antiserum containing 0.05% sodium azide and 30% glycerol.
Antiserum
Stockage et stabilité
2 years at -20°C from date of shipment
Informations légales
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
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)
Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".
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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency.
Thapa, A; Morris, L; Xu, J; Ma, H; Michalakis, S; Biel, M; Ding, XQ
The Journal of Biological Chemistry null
Cluster analysis reveals differential transcript profiles associated with resistance training-induced human skeletal muscle hypertrophy.
Thalacker-Mercer, A; Stec, M; Cui, X; Cross, J; Windham, S; Bamman, M
Physiological Genomics null
Anton Eberharter et al.
EMBO reports, 3(3), 224-229 (2002-03-08)
The organization of eukaryotic chromatin has a major impact on all nuclear processes involving DNA substrates. Gene expression is affected by the positioning of individual nucleosomes relative to regulatory sequence elements, by the folding of the nucleosomal fiber into higher-order
Raffaella Gatta et al.
Epigenetics, 6(4), 526-534 (2011-02-10)
Histones post-translational modifications (PTMs) are crucial for transcriptional control, defining positive and negative chromatin territories. We previously described an extensive methylation-acetylation switch on cell cycle promoters using a single nucleosome ChIP assay. A key issue is how PTMs are locally
James N Psathas et al.
Molecular and cellular biology, 29(24), 6413-6426 (2009-10-14)
Posttranslational modifications to histones have been studied extensively, but the requirement for the residues within the tails for different stages of transcription is less clear. Using RNR3 as a model, we found that the residues within the N terminus of
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