Anti-GPVI 抗体 [EPR25283-14] - BSA and Azide free (ab289987)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR25283-14] to GPVI - BSA and Azide free
- Suitable for: WB, IHC-P, Flow Cyt, IHC-Fr, IP
- Reacts with: Mouse
Related conjugates and formulations
製品の概要
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製品名
Anti-GPVI antibody [EPR25283-14] - BSA and Azide free
GPVI 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR25283-14] to GPVI - BSA and Azide free -
由来種
Rabbit -
アプリケーション
適用あり: WB, IHC-P, Flow Cyt, IHC-Fr, IPmore details -
種交差性
交差種: Mouse -
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: Mouse platelet lysate. IHC-P: Mouse spleen tissue. IHC-Fr: Mouse spleen (fresh) tissue. Flow cyt: Mouse blood cells. IP: Mouse platelet lysate.
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特記事項
ab289987 is the carrier-free version of ab289964.
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
EPR25283-14 -
アイソタイプ
IgG -
研究分野
関連製品
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Compatible Secondaries
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Isotype control
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ab289987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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WB |
Use at an assay dependent concentration. Detects a band of approximately 58 kDa (predicted molecular weight: 37 kDa).
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IHC-P |
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
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Flow Cyt |
Use at an assay dependent concentration.
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IHC-Fr |
Use at an assay dependent concentration.
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IP |
Use at an assay dependent concentration.
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特記事項 |
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WB
Use at an assay dependent concentration. Detects a band of approximately 58 kDa (predicted molecular weight: 37 kDa). |
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Flow Cyt
Use at an assay dependent concentration. |
IHC-Fr
Use at an assay dependent concentration. |
IP
Use at an assay dependent concentration. |
ターゲット情報
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機能
Collagen receptor involved in collagen-induced platelet adhesion and activation. Plays a key role in platelet procoagulant activity and subsequent thrombin and fibrin formation. This procoagulant function may contribute to arterial and venous thrombus formation. The signaling pathway involves the FcR gamma-chain, the Src kinases (likely Fyn/Lyn), the adapter protein LAT and leads to the activation of phospholipase C gamma2. -
組織特異性
Megakaryocytes and platelets. -
関連疾患
Bleeding disorder, platelet-type 11 -
配列類似性
Contains 2 Ig-like C2-type (immunoglobulin-like) domains. -
翻訳後修飾
N-linked glycosylation at Asn-92 is not required for the cell surface expression, but contributes to maximal adhesion to type I collagen, collagen-related peptide (CRP), and, to a lesser extent, to the snake venom C-type lectin convulxin (CVX). -
細胞内局在
Cell membrane. - Information by UniProt
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参照データベース
- Entrez Gene: 243816 Mouse
- SwissProt: P0C191 Mouse
- Unigene: 248662 Mouse
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別名
- Glycoprotein 6 antibody
- Glycoprotein VI antibody
- GP6 antibody
see all
画像
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling GPVI with ab289964 at 1/500 dilution followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Cytoplasmic staining on megakaryocytes and platelets of mouse spleen. The section was incubated with ab289964 at 4°C overnight. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0).
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh) tissue labeling GPVI with ab289964 at 1/100 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Positive staining in megakaryocytes of mouse spleen is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse blood cells cells labelling GPVI with ab289964 at 1/500 dilution (0.1µg)(Right) compared with a Rabbit monoclonal IgG (ab172730) isotype control (Left). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) was used as secondary antibody at 1/2000 dilution. Cells were stained with rabbit IgG or ab289964. Then stained with anti-CD41 conjµgated to APC. Gated on viable cells.
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All lanes : Anti-GPVI antibody [EPR25283-14] (ab289964) at 1/1000 dilution
Lane 1 : Mouse platelet lysate
Lane 2 : Mouse cerebellum tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/50000 dilution
Predicted band size: 37 kDa
Observed band size: 58 kDa why is the actual band size different from the predicted?This data was developed using 289964, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 23112346, 16014566).
Negative control: cerebellum. (PMID: 10961879).
Exposure time: 70 seconds.
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
GPVI was immunoprecipitated from Mouse platelet lysate with ab289964 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289964 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: Mouse platelet lysate 10 µg
Lane 2: ab289964 IP in Mouse platelet lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab289964 in mouse platelet lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 15 seconds
The expression profile/ molecµlar weight observed is consistent with what has been described in the literature (PMID: 23112346, PMID: 9295288).
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Anti-GPVI antibody [EPR25283-14] (ab289964) at 1/1000 dilution + Mouse platelet lysate at 20 µg
Secondary
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/50000 dilution
Predicted band size: 37 kDaThis data was developed using 289964, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID:�23112346, PMID:�16014566 ).
114 seconds
Exposure time:
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh) tissue labeling GPVI with ab289964 at 1/100 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Negative control (PMID: 10961879). No staining on mouse cerebellum is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
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This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling GPVI with ab289964 at 1/500 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Negative control: no staining on mouse cerebrum PMID 10961879). The section was incubated with ab289964 at 4°C overnight. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0).
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 (0)
ab289987 は論文での使用が確認できていません。