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AB243865

Anti-BRD2 抗体 [BL-167-2A2]

Anti-BRD2 antibody [BL-167-2A2]

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(2 Publications)

Knockout Tested Rabbit Recombinant Monoclonal BRD2 antibody. Suitable for IP, WB and reacts with Human, Mouse samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human BRD2 aa 650 to C-terminus.

別名を表示する

KIAA9001, RING3, BRD2, Bromodomain-containing protein 2, O27.1.1

5 Images
Immunoprecipitation - Anti-BRD2 antibody [BL-167-2A2] (AB243865)
  • IP

Unknown

Immunoprecipitation - Anti-BRD2 antibody [BL-167-2A2] (AB243865)

BRD2 was immunoprecipitated from 0.5 mg HEK-293T whole cell lysate with ab243865 at 10 µl per reaction Western blot was performed on the immunoprecipitate using ab243865 at 1/1000 dilution. Lane 1 : ab243865 IP in HEK-293T cell lysate.

Lane 2 : Contol IgG in HEK-293T cell lysate.

Detection : Chemiluminescence with an exposure time of 3 minutes.

All lanes:

Immunoprecipitation - Anti-BRD2 antibody [BL-167-2A2] (ab243865)

Predicted band size: 88 kDa

false

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)
  • WB

Lab

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)

False colour image of Western blot : Anti-BRD2 antibody [BL-167-2A2] staining at 1/1000 dilution, shown in green; Mouse Anti-Nucleophosmin antibody [FC82291] (ab10530) loading control staining at 2 ug/mL imaged in ECL. In Western blot, ab243865 was shown to bind specifically to BRD2. A band was observed at 110 kDa in wild-type A549 cell lysates with no signal observed at this size in BRD2 knockout cell line. To generate this image, wild-type and BRD2 knockout A549 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3% milk in TBS-0.1% Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4°C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times before development with Optiblot (ECL reagent ab133456) and imaged with 20 seconds exposure time. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and HRP conjugated Goat anti-Mouse (H+L) at 1/20000 dilution.

All lanes:

Western blot - Anti-BRD2 antibody [BL-167-2A2] (ab243865) at 1/1000 dilution

Lane 1:

Wild-type A549 cytoplasm cell lysate at 20 µg

Lane 2:

Wild-type A549 nuclear cell lysate at 20 µg

Lane 3:

BRD2 knockout A549 C7 cytoplasm cell lysate at 20 µg

Lane 4:

BRD2 knockout A549 C7 nuclear cell lysate at 20 µg

Lane 5:

Wild-type HEK-293T cell lysate at 20 µg

Lane 6:

BRD2 knockout HEK-293T cell lysate at 20 µg

false

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)
  • WB

Lab

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)

Lanes 1-3 : Merged signal (red and green). Green - ab243865 observed at 110 kDa. Red - loading control ab8245 observed at 36 kDa.

ab243865 Anti-BRD2 antibody [BL-167-2A2] was shown to specifically react with BRD2 in wild-type HEK293T cells. Loss of signal was observed when knockout cell line ab267265 (knockout cell lysate ab257191) was used. Wild-type and BRD2 knockout samples were subjected to SDS-PAGE. ab243865 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated at room temperature for 2. 5 hours at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.

All lanes:

Western blot - Anti-BRD2 antibody [BL-167-2A2] (ab243865) at 1/1000 dilution

Lane 1:

Wild-type HEK293T cell lysate at 20 µg

Lane 2:

BRD2 knockout HEK293T cell lysate at 20 µg

Lane 2:

Western blot - Human BRD2 knockout HEK-293T cell line (<a href='/products/cell-lines/human-brd2-knockout-hek-293t-cell-line-ab267265'>ab267265</a>)

Lane 3:

HeLa cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/10000 dilution

Predicted band size: 88 kDa

Observed band size: 110 kDa

false

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)
  • WB

Supplier Data

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)

All lanes:

Western blot - Anti-BRD2 antibody [BL-167-2A2] (ab243865) at 1/1000 dilution

Lane 1:

HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate at 50 µg

Lane 2:

MCF7 (Human breast adenocarcinoma cell line) whole cell lysate at 50 µg

Lane 3:

Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 50 µg

Lane 4:

A549 (Human lung carcinoma cell line) whole cell lysate at 50 µg

Lane 5:

SW620 (Human colon carcinoma cell line) whole cell lysate at 50 µg

Lane 6:

SK-MEL-28 (Human melanoma cell line) whole cell lysate at 50 µg

Lane 7:

Jurkat (Human T cell leukemia cell line from peripheral blood) whole cell lysate at 50 µg

Secondary

All lanes:

Goat anti-rabbit IgG, HRP conjugated

Predicted band size: 88 kDa

false

Exposure time: 30s

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)
  • WB

Supplier Data

Western blot - Anti-BRD2 antibody [BL-167-2A2] (AB243865)

All lanes:

Western blot - Anti-BRD2 antibody [BL-167-2A2] (ab243865) at 1/1000 dilution

Lane 1:

RenCa (Mouse epithelial kidney cell line) whole cell lysate at 50 µg

Lane 2:

NIH/3T3 (Mouse embryonic fibroblast cell line) whole cell lysate at 50 µg

Lane 3:

C2C12 (Mouse myoblast cell line) whole cell lysate at 50 µg

Secondary

All lanes:

Goat anti-rabbit IgG, HRP conjugated

Predicted band size: 88 kDa

false

Exposure time: 3s

Key facts

宿主種

Rabbit

クローン性

Monoclonal

クローン番号

BL-167-2A2

アイソタイプ

IgG

キャリアフリー

No

交差種

Human, Mouse

アプリケーション

IP, WB

applications

免疫原

Synthetic Peptide within Human BRD2 aa 650 to C-terminus. The exact immunogen used to generate this antibody is proprietary information.

P25440

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IP" : {"fullname" : "Immunoprecipitation", "shortname":"IP"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IP-species-checked": "testedAndGuaranteed", "IP-species-dilution-info": "", "IP-species-notes": "<p>Use 10μl/0.5mg lysate.</p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/1000", "WB-species-notes": "<p></p>" }, "Mouse": { "IP-species-checked": "guaranteed", "IP-species-dilution-info": "", "IP-species-notes": "", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/1000", "WB-species-notes": "<p></p>" } } }

製品の詳細

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

This product is sold under License from Bethyl Laboratories, Inc.

出荷温度及び保存条件

製品の状態
Liquid
精製に関する特記事項
Recombinant antibody was purified from cell culture supernatant.
バッファー組成
pH: 7.8 - 8.6 Preservative: 0.09% Sodium azide Constituents: 98% Borate buffered saline, 0.1% BSA
出荷温度
Blue Ice
短期保存期間
1-2 weeks
短期保存温度
+4°C
長期保存温度
+4°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle

製品プロトコール

For this product, it's our understanding that no specific protocols are required. You can visit:

ターゲットの情報

Chromatin reader protein that specifically recognizes and binds histone H4 acetylated at 'Lys-5' and 'Lys-12' (H4K5ac and H4K12ac, respectively), thereby controlling gene expression and remodeling chromatin structures (PubMed : 17148447, PubMed : 17848202, PubMed : 18406326, PubMed : 20048151, PubMed : 20709061, PubMed : 20871596). Recruits transcription factors and coactivators to target gene sites, and activates RNA polymerase II machinery for transcriptional elongation (PubMed : 28262505). Plays a key role in genome compartmentalization via its association with CTCF and cohesin : recruited to chromatin by CTCF and promotes formation of topologically associating domains (TADs) via its ability to bind acetylated histones, contributing to CTCF boundary formation and enhancer insulation (PubMed : 35410381). Also recognizes and binds acetylated non-histone proteins, such as STAT3 (PubMed : 28262505). Involved in inflammatory response by regulating differentiation of naive CD4(+) T-cells into T-helper Th17 : recognizes and binds STAT3 acetylated at 'Lys-87', promoting STAT3 recruitment to chromatin (PubMed : 28262505). In addition to acetylated lysines, also recognizes and binds lysine residues on histones that are both methylated and acetylated on the same side chain to form N6-acetyl-N6-methyllysine (Kacme), an epigenetic mark of active chromatin associated with increased transcriptional initiation (PubMed : 37731000). Specifically binds histone H4 acetyl-methylated at 'Lys-5' and 'Lys-12' (H4K5acme and H4K12acme, respectively) (PubMed : 37731000).
See full target information BRD2

文献 (2)

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Signal transduction and targeted therapy 8:302 PubMed37582812

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CDK7-YAP-LDHD axis promotes D-lactate elimination and ferroptosis defense to support cancer stem cell-like properties.

Applications

Unspecified application

Species

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Mengzhu Lv,Ying Gong,Xuesong Liu,Yan Wang,Qingnan Wu,Jie Chen,Qingjie Min,Dongyu Zhao,Xianfeng Li,Dongshao Chen,Di Yang,Danna Yeerken,Rui Liu,Jinting Li,Weimin Zhang,Qimin Zhan

Cell discovery 9:47 PubMed37156794

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BRD4-targeting PROTAC as a unique tool to study biomolecular condensates.

Applications

Unspecified application

Species

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Yi Shi,Yuan Liao,Qianlong Liu,Zhihao Ni,Zhenzhen Zhang,Minglei Shi,Pilong Li,Haitao Li,Yu Rao
View all publications

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