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※サムネイル画像をクリックすると拡大画像が表示されます。
Figure 1. Western blot analysis of Ankyrin erythroid/ANK/ANK1 using anti-Ankyrin erythroid/ANK/ANK1 antibody (M02716-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-Ankyrin erythroid/ANK/ANK1 antigen affinity purified monoclonal antibody (Catalog # M02716-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001) with Tanon 5200 system. A specific band was detected for Ankyrin erythroid/ANK/ANK1 at approximately 206 kDa. The expected band size for Ankyrin erythroid/ANK/ANK1 is at 206 kDa.
Figure 2. Flow Cytometry analysis of K562 cells using anti-Ankyrin erythroid/ANK/ANK1 antibody (M02716-1). Overlay histogram showing K562 cells stained with M02716-1 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with mouse anti-Ankyrin erythroid/ANK/ANK1 Antibody (M02716-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLightR488 conjugated goat anti-mouse IgG (BA1126, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
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Figure 1. Western blot analysis of Ankyrin erythroid/ANK/ANK1 using anti-Ankyrin erythroid/ANK/ANK1 antibody (M02716-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-Ankyrin erythroid/ANK/ANK1 antigen affinity purified monoclonal antibody (Catalog # M02716-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001) with Tanon 5200 system. A specific band was detected for Ankyrin erythroid/ANK/ANK1 at approximately 206 kDa. The expected band size for Ankyrin erythroid/ANK/ANK1 is at 206 kDa.
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| 別品名 |
Ankyrin-1, ANK-1, Ankyrin-R, Erythrocyte ankyrin, ANK1
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| 種由来 |
Human
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| 交差種 |
Human
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| 適用 |
Western Blot Flow Cytometry
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| 免疫動物 |
Mouse
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| クローン |
5H2E8
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| 抗原部位 |
a.a.1300-1844
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| 精製度 |
Affinity Purified
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| GENE ID |
286
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| Accession No.(Gene/Protein) |
P16157
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| 分子量 |
206265
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| メーカー |
品番 |
包装 |
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ABH
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ABO16594
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100 UG
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※表示価格について
| 当社在庫 |
なし
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| 納期目安 |
2週間程度
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| 保存温度 |
-20℃
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