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Key Documents

07-373

Sigma-Aldrich

Anti-acetyl-Histone H2B Antibody

Upstate®, from rabbit

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250 ML
CN¥2,105.25

CN¥2,105.25


Estimated to ship onNovember 17, 2025Details


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250 ML
CN¥2,105.25

About This Item

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

CN¥2,105.25


Estimated to ship onNovember 17, 2025Details


Request a Bulk Order

biological source

rabbit

Quality Level

antibody form

purified antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human

manufacturer/tradename

Upstate®

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

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I85071935105S06052
碘甲烷 (stabilised) for synthesis

806064

碘甲烷

碘甲烷 contains copper as stabilizer, ReagentPlus®, 99%

I8507

碘甲烷

碘甲烷 SAJ first grade, ≥93.0%

193510

碘甲烷

vapor pressure

24.09 psi ( 55 °C)

vapor pressure

24.09 psi ( 55 °C), 7.89 psi ( 20 °C)

vapor pressure

24.09 psi ( 55 °C), 7.89 psi ( 20 °C)

vapor pressure

-

assay

≥99.0% (GC)

assay

99%

assay

≥93.0%

assay

-

form

liquid

form

liquid

form

liquid

form

-

potency

79.84 mg/kg LD50, oral (rat)

potency

-

potency

-

potency

-

expl. lim.

8.5-66 % (v/v)

expl. lim.

-

expl. lim.

-

expl. lim.

-

Specificity

acetylated Histone H2B

Immunogen

Synthetic peptide in which there is an acetyl-lysine at residues 5, 12, 15 and 20 of human Histone H2B

Application

Detect acetyl-Histone H2B also known as Histone H2B with Anti-acetyl-Histone H2B Antibody (Rabbit Polyclonal Antibody), that has been demonstrated to work in WB.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones

Quality

routinely evaluated by immunoblot in sodium butyrate treated, acid extracted proteins from HeLa cells

Target description

15 kDa

Physical form

0.1M Tris-glycine, pH 7.4, 0.15M NaCl, 0.05% sodium azide before the addition of glycerol to 30%
Format: Purified
Protein A chromatography

Storage and Stability

2 years at -20°C

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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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Storage Class Code

10 - Combustible liquids

WGK

WGK 1


Certificates of Analysis (COA)

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Spatial memory consolidation is associated with induction of several lysine-acetyltransferase (histone acetyltransferase) expression levels and H2B/H4 acetylation-dependent transcriptional events in the rat hippocampus.
Bousiges, O; Vasconcelos, AP; Neidl, R; Cosquer, B; Herbeaux, K; Panteleeva, I; Loeffler et al.
Neuropsychopharmacology null
Snehajyoti Chatterjee et al.
EMBO molecular medicine, 10(11) (2018-10-03)
Chromatin acetylation, a critical regulator of synaptic plasticity and memory processes, is thought to be altered in neurodegenerative diseases. Here, we demonstrate that spatial memory and plasticity (LTD, dendritic spine formation) deficits can be restored in a mouse model of
A novel activator of CBP/p300 acetyltransferases promotes neurogenesis and extends memory duration in adult mice.
Chatterjee, S; Mizar, P; Cassel, R; Neidl, R; Selvi, BR; Mohankrishna, DV; Vedamurthy et al.
The Journal of Neuroscience null
Lucie Crouzier et al.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 39, 29-45 (2020-09-08)
The sigma-1 receptor (S1R) is a membrane-associated protein expressed in neurons and glia at mitochondria-associated endoplasmic reticulum (ER) membranes (MAMs). S1R interacts with different partners to regulate cellular responses, including ER stress, mitochondrial physiology and Ca2+ fluxes. S1R shapes cellular
Frederick A Schroeder et al.
PloS one, 8(8), e71323-e71323 (2013-08-24)
Psychiatric diseases, including schizophrenia, bipolar disorder and major depression, are projected to lead global disease burden within the next decade. Pharmacotherapy, the primary--albeit often ineffective--treatment method, has remained largely unchanged over the past 50 years, highlighting the need for novel

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