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- 详细信息
- 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
- 保质期:
1 year
- 级别:
科研级
- 库存:
99999
- 供应商:
AntibodySystem
- 宿主:
Mouse
- 应用范围:
WB
- 浓度:
1 mg/ml
- 靶点:
Adenosine aminohydrolase, Adenosine deaminase, ADA1, ADA
- 抗体英文名:
Anti-ADA/Adenosine deaminase Antibody (R2W87)
- 抗体名:
Anti-ADA/Adenosine deaminase Antibody (R2W87)
- 规格:
100 μg

| Clonality | Monoclonal |
| Species reactivity | Human |
| Host species | Mouse |
| Isotype | IgG1 |
| Conjugation | |
| Tested applications | WB: 1:500-1:1000 |
| Applications | 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 | Adenosine aminohydrolase, Adenosine deaminase, ADA1, ADA |
| Purification | Protein A/G purified from cell culture supernatant. |
| Endotoxin level | Please contact with the lab for this information. |
| Accession | P00813 |
| 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 | R2W87 |
| Note | For research use only. |
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文献和实验A 腺苷脱氨酶缺乏症 adenosine deaminase deficiency (ADA) 腺病毒 adenovirus Alagille综合征 Alagille syndrome 等位基因 allele 氨基酸 amino acids 动物模型 animal model 抗体 antibody 凋亡 apoptosis 路-巴综合征 ataxia-telangiectasia 常染色体显性 autosomal dominant 常染色体 autosome B
of soluble cAMP in bacterial extracts to compete with binding of an alkaline phosphatase (AP)-conjugated anti-cAMP antibody to immobilized cAMP. The surface-bound, immobilized anti-cAMP-AP is inversely correlated to the concentration of cAMP in the extract
。但直到1990年才成功地实现了用基因治疗手段尝试治疗腺苷酸脱氨酶缺乏症(adenosine deaminase deficiency)。到目前为止,已报道的基因治疗方案已超过百种。有300多病人接受了这种新的治疗方式。基因治疗的对象不再局限于遗传病,而被扩展到肿瘤和传染病等多种疾病。其发展相当迅速,前景十分看好,我国学者也在用基因治疗方式治疗血友病方面做了一定工作。目前已积累了一定的经验和教训,有了一些可遵循的操作程序及可供选择的治疗方式。但这种新的治疗方式仍有许多环节需要不断改进和提高。
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