Skip to Content
Merck
All Photos(3)

Key Documents

Safety Information

ABE1451

Sigma-Aldrich

Anti-phospho BRD4 (Ser492)

from rabbit

Synonym(s):

Bromodomain-containing protein 4, MCAP, Mitotic chromosome-associated protein, Protein HUNK1

Sign Into View Organizational & Contract Pricing


About This Item

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

biological source

rabbit

Quality Level

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

mouse, human

species reactivity (predicted by homology)

rat (based on 100% sequence homology)

technique(s)

dot blot: suitable
immunocytochemistry: suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

phosphorylation (pSer492)

Gene Information

human ... BRD4(23476)

General description

Bromodomain-containing protein 4 (UniProt O60885; also known as MCAP, Mitotic chromosome-associated protein, Protein HUNK1) is encoded by the BRD4 (also known as HUNK1, MCAP) gene (Gene ID 23476) in human. BRD4 is a BET (bromodomain and extra-terminal) protein family member that functions as a chromatin reader by binding acetylated lysines in histones. BRD4 is an important transcription regulator in many cell types, including transcription in response to external cues. BRD4 plays an essential role in neuronal function and mediates the transcriptional regulation underlying learning and memory. BRD4 regulates IEG transcription in neurons upon phosphorylation by casein kinase 2 (CK2), which is activated in response to neuronal stimulation. Brd4 knockout in mice is lethal, while Brd4 function blockage by inhibitor JQ1 (Cat. No. 500586) treatment is reported to affect the transcription of critical synaptic proteins, resulting in memory deficits and decreased seizure susceptibility in mice.

Specificity

The target phospho-serine residue is present in all human (pSer492) and murine (pSer493) BRD4 spliced isoforms reported by UniProt (O60885 and Q9ESU6). This polyclonal antibody is shown to exhibit stronger immunoreactivity toward BRD4 phosphopeptide with dual pSer492/494 (equivalent to mouse pSer493/495) phosphorylation than the corresponding peptide with only pSer492 (equivalent to mouse Ser493) phosphorylation (Korb, E., et al. (2015). Nat. Neurosci. 18(10):1464-1473).

Immunogen

KLH-conjugated linear peptide corresponding to a human BRD4 sequence containing phosphorylated Ser492 (equivalent to mouse Ser493).

Application

Detect BRD4 Serine 492 phosphorylation using this rabbit polyclonal Anti-phospho BRD4 (Ser492), Cat. No. ABE1451, validated for use in Immunocytochemistry, Dot Blot and Western Blotting.
Immunocytochemistry Analysis: A 1:500 dilution from a representative lot detected nuclear Brd4 pSer493 (equivalent to human Ser492) immunoreactivity in 12-day cultured E16.5 embryonic mouse cortical neurons (Courtesy of Erica Korb, Ph.D. Rockefeller University, New York, U.S.A.).University, New York, U.S.A.).

Western Blotting Analysis: A 1:500 dilution from a representative lot detected Brd4 Ser493 (equivalent to human Ser492) phosphorylation in lysate from 12-day cultured E16.5 embryonic mouse cortical neurons. Prior phosphatase treatment of the lysate abolished target band detection (Courtesy of Erica Korb, Ph.D. Rockefeller University, New York, U.S.A.).

Dot Blot Analysis: A representative lot detected BRD4 phosphopeptide with pSer492 or dual pSer492/494 phosphorylation (equivalent to mouse Ser493/495), but not the corresponding non-phosphorylated peptide or peptide with only pSer494 phosphorylation (Korb, E., et al. (2015). Nat. Neurosci. 18(10):1464-1473).

Western Blotting Analysis: A representative lot detected Brd4 Ser493 (equivalent to human Ser492) phosphorylation induction upon BDNF stimulation of cultured E16.5 embryonic mouse cortical neurons from C57BL/6 mice. Pre-treatment of neurons with CK2 inhibitor 4,5,6,7-tetrabromobenzotriazole (TBB; Cat. No. 218697) before BDNF stimulation or phosphatase treatment of the lysate prior to immunoblotting abolished target band detection (Korb, E., et al. (2015). Nat. Neurosci. 18(10):1464-1473).
Research Category
Epigenetics & Nuclear Function

Quality

Evaluated by Western Blotting in human iPSC lysate.

Western Blotting Analysis: A 1:1000 dilution of this antibody detected Brd4 Ser492 phosphorylation in 10 µg of human induced pluripotent stem cell (iPSC) lysate.

Target description

~140/200 kDa observed. 152.2/155.9 kDa (human/mouse isoform Long), 80.46/80.61 kDa (human/mouse isoform Short), 88.29 kDa (human isoform B) calculated. Uncharacterized bands may be observed in some lysate(s).

Physical form

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

Storage and Stability

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

Other Notes

Concentration: Please refer to lot specific datasheet.

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.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

ABE1451:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yu-Ting Yen et al.
Communications biology, 4(1), 658-658 (2021-06-04)
It has not been well studied which cells and related mechanisms contribute to endochondral ossification. Here, we fate mapped the leptin receptor-expressing (LepR+) mesenchymal stem cells (MSCs) in different embryonic and adult extremities using Lepr-cre; tdTomato mice and investigated the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service