- ￥2450
- AntibodySystem
- France
- RHJ56403
- 2025年07月15日
- ELISA, IHC, WB
- Mouse
- Human, Mouse, Rat, Monkey
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- 文献和实验
- 技术资料
- 亚型：
IgG1
- 形态：
Liquid
- 保存条件：
0.01M PBS, pH 7.4, 0.05% Sodium Azide.
- 克隆性：
Monoclonal
- 适应物种：
Human, Mouse, Rat, Monkey
- 保质期：
1 year
- 级别：
科研级
- 库存：
99999
- 供应商：
AntibodySystem
- 宿主：
Mouse
- 应用范围：
ELISA, IHC, WB
- 浓度：
1 mg/ml
- 靶点：
Keratinocyte transcription factor KET, P63, KET, Tumor protein p73-like, p63, P73L, CUSP, P73H, p40, Tumor protein 63, TP73L, Transformation-related protein 63, TP63, Chronic ulcerative stomatitis protein, p73L, p51
- 抗体英文名：
Anti-TP63/p40 Antibody (R3W46)
- 抗体名：
Anti-TP63/p40 Antibody (R3W46)
- 规格：
100 μg
| Clonality | Monoclonal |
| Species reactivity | Human, Mouse, Rat, Monkey |
| Host species | Mouse |
| Isotype | IgG1 |
| Conjugation | |
| Tested applications | ELISA: 1:10000, IHC: 1:200-1:1000, WB: 1:500-1:2000 |
| Applications | ELISA, IHC, WB |
| Form | Liquid |
| Storage buffer | 0.01M PBS, pH 7.4, 0.05% Sodium Azide. |
| Concentration | 1 mg/ml |
| Purity | >95% as determined by SDS-PAGE. |
| Target | Keratinocyte transcription factor KET, P63, KET, Tumor protein p73-like, p63, P73L, CUSP, P73H, p40, Tumor protein 63, TP73L, Transformation-related protein 63, TP63, Chronic ulcerative stomatitis protein, p73L, p51 |
| Purification | Protein A/G purified from cell culture supernatant. |
| Endotoxin level | Please contact with the lab for this information. |
| Accession | Q9H3D4 |
| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| Clone ID | R3W46 |
| Note | For research use only. |
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文献和实验Simultaneous analysis of DNA content and surface immunophenotype using gentle ethanol fixation&
preservation of surface markers. References Fraker, P.J., King, L.E., Lill-Elghanian, D. and Telford, W.G. (1994) Quantitation of apoptotic events in pure and heterogeneous populations of cells using flow cytometry. In Methods in Cell Biology Volume 46
Simultaneous analysis of DNA content and surface
content with simultaneous preservation of cell surface markers, we have utilized gentle ethanol treatment techniques, which permeablize cells with minimal loss of surface antigen expression and antibody-antigen association. For some cell types
Identification of Legionella in Clinical Samples
Microbiol 46:671–677, 2008). The isolation of Legionella strains from pulmonary samples by axenic culture is still required to perform further epidemiological investigations (Blyth et al., N S W Public Health Bull 20:157–161, 2009; Fields et al., Clin
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