Anti-TRAF1 抗体 [EPR26204-112] (BSA and Azide free) (ab300076)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR26204-112] to TRAF1 - BSA and Azide free
- Suitable for: IP, IHC-P, WB
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free)
TRAF1 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR26204-112] to TRAF1 - BSA and Azide free -
由来種
Rabbit -
アプリケーション
適用あり: IP, IHC-P, WBmore details
適用なし: Flow Cyt or ICC/IF -
種交差性
交差種: Mouse, Rat, Human -
免疫原
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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ポジティブ・コントロール
- WB: Whole cell fresh lysates Raji (human Burkitt's lymphoma B lymphocyte), whole cell lysates of: Ramos (human Burkitt's lymphoma B lymphocyte), Daudi (human Burkitt's lymphoma lymphoblast), Daudi whole cell fresh lysate, human tonsil and lymphoma tissue lysate.
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特記事項
ab300076 is a cvarrier free version of ab300075.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with <1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
製品の特性
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製品の状態
Liquid -
保存方法
Shipped at 4°C. Store at +4°C. -
バッファー
pH: 7.2
Constituent: 100% PBS -
キャリア・フリー
はい -
Concentration information loading...
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精製度
Protein A purified -
ポリ/モノ
モノクローナル -
クローン名
EPR26204-112 -
アイソタイプ
IgG -
研究分野
関連製品
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Alternative Versions
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Compatible Secondaries
アプリケーション
The Abpromise guarantee
Abpromise保証は、 次のテスト済みアプリケーションにおけるab300076の使用に適用されます
アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。
アプリケーション | Abreviews | 特記事項 |
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IP |
Use at an assay dependent concentration.
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IHC-P |
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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WB |
Use at an assay dependent concentration. Detects a band of approximately 50 kDa (predicted molecular weight: 46 kDa).
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特記事項 |
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IP
Use at an assay dependent concentration. |
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
WB
Use at an assay dependent concentration. Detects a band of approximately 50 kDa (predicted molecular weight: 46 kDa). |
ターゲット情報
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機能
Adapter molecule that regulates the activation of NF-kappa-B and JNK. Plays a role in the regulation of cell survival and apoptosis. The heterotrimer formed by TRAF1 and TRAF2 is part of a E3 ubiquitin-protein ligase complex that promotes ubiquitination of target proteins, such as MAP3K14. The TRAF1/TRAF2 complex recruits the antiapoptotic E3 protein-ubiquitin ligases BIRC2 and BIRC3 to TNFRSF1B/TNFR2. -
配列類似性
Contains 1 MATH domain. -
ドメイン
The coiled coil domain mediates homo- and hetero-oligomerization.
The MATH/TRAF domain binds to receptor cytoplasmic domains.
Cleavage by CASP8 liberates a C-terminal fragment that promotes apoptosis and inhibits the activation of NF-kappa-B in response to TNF signaling. -
翻訳後修飾
Polyubiquitinated by BIRC2 and/or BIRC3, leading to its subsequent proteasomal degradation. - Information by UniProt
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参照データベース
- Entrez Gene: 7185 Human
- Entrez Gene: 22029 Mouse
- Entrez Gene: 687813 Rat
- Omim: 601711 Human
- SwissProt: Q13077 Human
- SwissProt: P39428 Mouse
- Unigene: 531251 Human
- Unigene: 239514 Mouse
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別名
- 4732496E14Rik antibody
- EBI6 antibody
- EBV induced protein 6 antibody
see all
画像
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This data was developed using ab300075, the same antibody clone in a different buffer formulation.
TRAF1 was immunoprecipitated from 0.35 mg Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg with ab300075 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300075 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg
Lane 2: ab300075 in Raji whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab300075 in Raji whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 10 seconds
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This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in rat spleen (PMID: 11046039). The section was incubated with ab300075 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in mouse spleen (PMID: 11046039). The section was incubated with ab300075 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
-
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse thymus tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on mouse thymus medulla (PMID: 11046039). The section was incubated with ab300075 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
-
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human thymus tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human thymus (PMID: 11046039). The section was incubated with ab300075 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
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This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human lymph node hyperplasia tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human lymph node hyperplasia (PMID: 11046039). The section was incubated with ab300075 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
-
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) was used. Cytoplasmic staining on Reed-Sternberg cells in human Hodgkin's lymphoma (PMID: 12502848). The section was incubated with ab300075 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
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All lanes : Anti-TRAF1 antibody [EPR26204-112] (ab300075) at 1/1000 dilution
Lane 1 : Raji (human Burkitt's lymphoma B lymphocyte) whole cell fresh lysate
Lane 2 : HEK-293 (human embryonic kidney epithelial cell) whole cell fresh lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 46 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?
Exposure time: 15 secondsThis data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and iluting buffer.
Lysates were freshly made and used in WB test immediately to minimize protein degradation.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 25321474, 25996949).
Negative control: HEK-293 (PMID: 12502848) -
All lanes : Anti-TRAF1 antibody [EPR26204-112] (ab300075) at 1/1000 dilution
Lane 1 : Ramos (human Burkitt's lymphoma B lymphocyte) whole cell lysate
Lane 2 : Daudi (human Burkitt's lymphoma lymphoblast) whole cell lysate
Lane 3 : Daudi whole cell fresh lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 46 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?This data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and iluting buffer.
Exposure time:
Lane 1-2: 92 seconds
Lane3: 3 minutesLeft-hand blot (lanes 1 & 2) was developed using a high sensitivity ECL substrate.
Lane 3: Lysates were freshly made and used in WB test immediately to minimize protein degradation.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 25321474, 25996949). -
All lanes : Anti-TRAF1 antibody [EPR26204-112] (ab300075) at 1/1000 dilution
Lane 1 : Human tonsil tissue lysate
Lane 2 : Human lymphoma tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Developed using the ECL technique.
Predicted band size: 46 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?
Exposure time: 92 secondsThis data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and diluting buffer.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 25321474, 25996949).
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
データシートおよび資料
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Datasheet download
Certificate of Compliance
参考文献 (1)
ab300076 は 1 報の論文で使用されています。
- Hong Y et al. Elabela inhibits TRAF1/NF-κB induced oxidative DNA damage to promote diabetic foot ulcer wound healing. iScience 26:107601 (2023). PubMed: 37664606