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Merck
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Documents

07-376

Sigma-Aldrich

Anti-acetyl-Histone H2A Antibody

serum, Upstate®

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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)

western blot: suitable

Isotype

IgG

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Spécificité

acetylated Histone H2A

Immunogène

peptide containing surrounding acetylated lysine residues 5, 9, 13 and 15 of human Histone H2A.

Application

Detect acetyl-Histone H2A also known as Histone H2A with Anti-acetyl-Histone H2A Antibody (Rabbit Polyclonal Antibody), that has been demonstrated to work in WB.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones

Qualité

routinely evaluated by immunoblot acid extracted proteins from sodium butyrate treated HeLa cells (Catalog # 13-113)

Description de la cible

14 kDa

Forme physique

0.05% sodium azide and 30% glycerol
Antiserum

Stockage et stabilité

2 years at -20°C

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

10-13 - German Storage Class 10 to 13


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Vahid Ebrahimi et al.
Optics express, 29(20), 32691-32699 (2021-10-08)
We demonstrate single-shot nondiffracting light-sheet microscopy by the incoherent superposition of dispersed polychromatic light sources. We characterized our technique by generating a Bessel light-sheet with a supercontinuum light-source and a C-light-sheet using a diode laser, and demonstrated its applicability to
Lauren Switala et al.
Journal of nanobiotechnology, 22(1), 223-223 (2024-05-04)
Cardiac muscle targeting is a notoriously difficult task. Although various nanoparticle (NP) and adeno-associated viral (AAV) strategies with heart tissue tropism have been developed, their performance remains suboptimal. Significant off-target accumulation of i.v.-delivered pharmacotherapies has thwarted development of disease-modifying cardiac
Jacopo Scrofani et al.
Molecular biology of the cell, 35(1), ar12-ar12 (2023-11-22)
Chromosome segregation relies on the correct assembly of a bipolar spindle. Spindle pole self-organization requires dynein-dependent microtubule (MT) transport along other MTs. However, during M-phase RanGTP triggers MT nucleation and branching generating polarized arrays with nonastral organization in which MT
Chi-Chuan Lin et al.
Molecular cell, 82(6), 1089-1106 (2022-03-02)
The recruitment of signaling proteins into activated receptor tyrosine kinases (RTKs) to produce rapid, high-fidelity downstream response is exposed to the ambiguity of random diffusion to the target site. Liquid-liquid phase separation (LLPS) overcomes this by providing elevated, localized concentrations
Wei Zhang et al.
Nature cell biology, 25(10), 1453-1464 (2023-09-29)
Integrin-mediated focal adhesions are the primary architectures that transmit forces between the extracellular matrix (ECM) and the actin cytoskeleton. Although focal adhesions are abundant on rigid and flat substrates that support high mechanical tensions, they are sparse in soft three-dimensional

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