Anti-HEPACAM 抗体 [EPR25296-150] (BSA and Azide free) (ab300572)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR25296-150] to HEPACAM
- Suitable for: WB, IHC-P
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-HEPACAM antibody [EPR25296-150] (BSA and Azide free)
HEPACAM 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR25296-150] to HEPACAM -
由来種
Rabbit -
アプリケーション
適用あり: WB, IHC-Pmore details
適用なし: Flow Cyt,ICC/IF,IHC-Fr 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: Whole cell lysates: Untreated HepG2 (human hepatocellular carcinoma epithelial cell), HepG2 (human hepatocellular carcinoma epithelial cell). Human, mouse and rat brain tissue lysates. IHC-P: Human, mouse, and rat cerebrum.
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特記事項
ab300572 is the carrier-free version of ab300571.
ab300571 does not react in IHC-Fr with mouse, flow cytometry with human and mouse, and immunoprecipitation with human.
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: 7.20
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
EPR25296-150 -
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ab300572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.
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IHC-P |
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. |
IHC-P
Use at an assay dependent concentration. |
ターゲット情報
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機能
Involved in regulating cell motility and cell-matrix interactions. May inhibit cell growth through suppression of cell proliferation. -
配列類似性
Contains 1 Ig-like C2-type (immunoglobulin-like) domain.
Contains 1 Ig-like V-type (immunoglobulin-like) domain. -
ドメイン
The cytoplasmic domain plays an important role in regulation of cell-matrix adhesion and cell motility. -
翻訳後修飾
N-glycosylated. -
細胞内局在
Cytoplasm. Membrane. In MCF7 breast carcinoma and hepatic Hep3B and HepG2 cell lines, localization of HEPACAM is cell density-dependent. In well spread cells, localized to punctate structures in the perinuclear membrane, cytoplasm, and at cell surface of protusions. In confluent cells, localized predominantly to the cytoplasmic membrane, particularly in areas of cell-cell contacts. Colocalizes with CDH1. - Information by UniProt
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参照データベース
- Entrez Gene: 220296 Human
- Entrez Gene: 72927 Mouse
- Omim: 611642 Human
- SwissProt: Q14CZ8 Human
- SwissProt: Q640R3 Mouse
- Unigene: 159863 Human
- Unigene: 266133 Mouse
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別名
- FLJ25530 antibody
- GlialCAM antibody
- HECAM_HUMAN antibody
see all
画像
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All lanes : Anti-HEPACAM antibody [EPR25296-150] (ab300571) at 1/2000 dilution
Lane 1 : HepG2 whole cell lysate treated with Protein Deglycosylation Mix II
Lane 2 : Untreated HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate
Lane 3 : HepG2 (human hepatocellar carcinoma epithelial cell) whole cell lysate 20
Lane 4 : LNCaP (human prostate carcinoma epithelial cell) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Performed under non-reducing conditions.
Observed band size: 46 kDa why is the actual band size different from the predicted?
Exposure time: 103 secondsThis data was developed using 300571, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: Negative control:LNCaP(PMID:29658567).
HEPACAM is a glycoprotein(PMID: 15885354) of approximately 46-72 kDa and detected as a 46 kDa band after treated with Protein Deglycosylation MIX II.
The samples are unboiled.
Exposure time: 103 seconds.
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All lanes : Anti-HEPACAM antibody [EPR25296-150] (ab300571) at 1/2000 dilution
Lane 1 : Mouse brain tissue lysate
Lane 2 : Rat brain tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Performed under non-reducing conditions.
Observed band size: 46-72 kDa why is the actual band size different from the predicted?
Exposure time: 81 secondsThis data was developed using 300571, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration:5% NFDM/TBST.
The samples are unboiled.
Exposure time: 81 seconds.
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Anti-HEPACAM antibody [EPR25296-150] (ab300571) at 1/2000 dilution + Human brain tissue lysate
Secondary
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 46-72 kDa why is the actual band size different from the predicted?This data was developed using 300571, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Exposure time: 15 seconds.
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This data was developed using ab300571, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling HEPACAM with ab300571 at 1/500 dilution (0.994 µg/mL), followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection kit). Cytoplasmic staining on human cerebrum. The section was incubated with ab300571 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: PBS was used instead of primary antibody, followed by a ready to use secondary antibody LeicaDS9800 (Bond™ Polymer Refine Detection kit).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.
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This data was developed using ab300571, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling HEPACAM with ab300571 at 1/500 dilution (0.994 µg/mL) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection kit). Cytoplasmic staining on mouse cerebrum is observed. The section was incubated with ab300571 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: PBS was used instead of primary antibody, followed by a ready to use secondary antibody LeicaDS9800 (Bond™ Polymer Refine Detection kit).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.
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This data was developed using ab300571, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling HEPACAM with ab300571 at 1/500 dilution (0.994 µg/mL) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection kit). Cytoplasmic staining on rat cerebrum is observed. The section was incubated with ab300571 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: PBS was used instead of primary antibody, followed by a ready to use secondary antibody LeicaDS9800 (Bond™ Polymer Refine Detection kit).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.
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This data was developed using ab300571, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human kidney tissue labeling HEPACAM with ab300571 at 1/500 dilution (0.994 µg/mL) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection kit). Negative control: No staining on human kidney is observed. The section was incubated with ab300571 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.
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)
ab300572 は論文での使用が確認できていません。