Anti-NPTXR + NPTX2 + NPTX1 抗体 [EPR25684-9] - BSA and Azide free (ab289870)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR25684-9] to NPTXR + NPTX2 + NPTX1 - BSA and Azide free
- Suitable for: WB, IHC-P, IHC-Fr
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-NPTXR + NPTX2 + NPTX1 antibody [EPR25684-9] - BSA and Azide free -
製品の詳細
Rabbit monoclonal [EPR25684-9] to NPTXR + NPTX2 + NPTX1 - BSA and Azide free -
由来種
Rabbit -
アプリケーション
適用あり: WB, IHC-P, IHC-Frmore details
適用なし: Flow Cyt,ICC/IF or IP -
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: IMR-32 whole cell lysate; Mouse brain tissue lysate; Rat brain tissue lysate; His-tagged human NPTXR recombinant protein fragment, His-tagged human NPTX1 full length recombinant protein (without signal peptide), recombinant human NPTX2 protein (without signal peptide). IHC-P: Human cerebrum tissue; Mouse cerebrum tissue; Rat cerebrum tissue. IHC-Fr: Mouse cerebrum (fresh) tissue; Rat cerebrum (fresh) tissue.
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特記事項
ab289870 is a carrier-free version of ab289861.
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
EPR25684-9 -
アイソタイプ
IgG -
研究分野
関連製品
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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ab289870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 |
---|---|---|
WB |
Use at an assay dependent concentration. Detects a band of approximately 30, 50 kDa (predicted molecular weight: 52 kDa).
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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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IHC-Fr |
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 30, 50 kDa (predicted molecular weight: 52 kDa). |
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. |
IHC-Fr
Use at an assay dependent concentration. |
ターゲット情報
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細胞内局在
NPTXR: Membrane. NPTX2: Secreted. NPTX1: Membrane. -
参照データベース
- Entrez Gene: 23467 Human
- Entrez Gene: 4885 Human
- Entrez Gene: 53324 Mouse
- Entrez Gene: 73340 Mouse
- Entrez Gene: 288475 Rat
- Entrez Gene: 81005 Rat
- Omim: 600750 Human
- Omim: 609474 Human
see all
画像
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This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling NPTXR+NPTX2+NPTX1 with ab289861 at 1/2000 dilution, followed by ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on human cerebrum. The section was incubated with ab289861 for 30 mins at room temperature.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins was used.
The immunostaining was performed on a Leica Biosystems BOND® RX instrumentCounter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse cerebrum (fresh) tissue labelling NPTXR+NPTX2+NPTX1 with ab289861 at 1/50 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution (Green). Positive staining on mouse cerebrum (fresh). The nuclear counterstain is DAPI (Blue).
Secondary antibody only control: Used PBS instead of primary antibody, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution.
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All lanes : Anti-NPTXR + NPTX2 + NPTX1 antibody [EPR25684-9] (ab289861) at 1/1000 dilution
Lane 1 : IMR-32 (Human neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 2 : HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 3 : Mouse brain tissue lysate at 20 µg
Lane 4 : Mouse skeletal muscle tissue lysate at 40 µg
Lane 5 : Mouse spleen tissue lysate at 20 µg
Lane 6 : Rat brain tissue lysate at 20 µg
Lane 7 : Rat skeletal muscle tissue lysate at 40 µg
Lane 8 : Rat spleen tissue lysate at 20 µg
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 52 kDa
Observed band size: 53 kDa why is the actual band size different from the predicted?This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBS.
Eposure times:
Lane1-2: 180 seconds;
Lane3-8: 70 seconds.Samples are non-boiled as boiling may cause protein aggregates.
The observed MW are consistent with what has been described in the literature (PMID: 32847597, PMID: 32273328, PMID: 28440221)
Low expression: Hela, skeletal muscle, spleen (PMID: 32847597, PMID: 32273328, PMID: 28440221)
The bands nearby 40 kDa could be non-specific bands. -
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling NPTXR+NPTX2+NPTX1 with ab289861 at 1/2000 dilution, followed by ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on mouse cerebrum. The section was incubated with ab289861 for 30 mins at room temperature.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins was used.
The immunostaining was performed on a Leica Biosystems BOND® RX instrumentCounter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
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All lanes : Anti-NPTXR + NPTX2 + NPTX1 antibody [EPR25684-9] (ab289861) at 1/1000 dilution
Lane 1 : His-tagged human NPTXR recombinant protein fragment 10ng
Lane 2 : His-tagged human NPTX1 full length recombinant protein (without signal peptide) 10ng
Lane 3 : Human NPTX2 full length recombinant protein (without signal peptide) 10ng
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 52 kDa
Observed band size: 30 kDa why is the actual band size different from the predicted?This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBS.
Eposure times: 5.5 seconds
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling NPTXR+NPTX2+NPTX1 with ab289861 at 1/2000 dilution, followed by ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on rat cerebrum. The section was incubated with ab289861 for 30 mins at room temperature.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins was used.
The immunostaining was performed on a Leica Biosystems BOND® RX instrumentCounter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse skeletal muscle (fresh) tissue labelling NPTXR+NPTX2+NPTX1 with ab289861 at 1/50 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution (Green). Negative control (PMID: 9261167). No staining on mouse skeletal muscle (fresh). The nuclear counterstain is DAPI (Blue).
Secondary antibody only control: Used PBS instead of primary antibody, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution.
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human liver tissue labeling NPTXR+NPTX2+NPTX1 with ab289861 at 1/2000 dilution, followed by ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Negative control: no staining on human liver. The section was incubated with ab289861 for 30 mins at room temperature.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins was used.
The immunostaining was performed on a Leica Biosystems BOND® RX instrumentCounter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat cerebrum (fresh) tissue labelling NPTXR+NPTX2+NPTX1 with ab289861 at 1/50 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution (Green). Positive staining on rat cerebrum. The nuclear counterstain is DAPI (Blue).
Secondary antibody only control: Used PBS instead of primary antibody, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution.
-
This data was developed using ab289861, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat skeletal muscle (fresh) tissue labelling NPTXR+NPTX2+NPTX1 with ab289861 at 1/50 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution (Green). Negative control (PMID: 9261167). No staining on rat skeletal muscle (fresh). The nuclear counterstain is DAPI (Blue).
Secondary antibody only control: Used PBS instead of primary antibody, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) secondary antibody at 1/1000 dilution.
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)
ab289870 は論文での使用が確認できていません。