CD59 抗体 (AA 26-128)
Quick Overview for CD59 抗体 (AA 26-128) (ABIN6138210)
抗原
See all CD59 抗体适用
宿主
克隆类型
标记
应用范围
- 
    - 
                                            抗原表位
- AA 26-128
- 
                                            序列
- LQCYNCPNPT ADCKTAVNCS SDFDACLITK AGLQVYNKCW KFEHCNFNDV TTRLRENELT YYCCKKDLCN FNEQLENGGT SLSEKTVLLL VTPFLAAAWS LHP
- 
                                            交叉反应
- 人, 小鼠
- 
                                            产品特性
- Polyclonal Antibodies
- 
                                            纯化方法
- Affinity purification
- 
                                            免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 26-128 of human CD59 (NP_001120695.1).
- 
                                            亚型
- IgG
 
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- 
    
- 
    - 
                                            应用备注
- WB,1:500 - 1:2000
- 
                                            说明
- 
                        HIGH QUALITY 
- 
                                            限制
- 仅限研究用
 
- 
                                            
- 
    - 
                                            状态
- Liquid
- 
                                            缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 
                                            储存液
- Sodium azide
- 
                                            注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 
                                            储存条件
- -20 °C
- 
                                            储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
 
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- 
    - CD59
- 
                                            别名
- CD59
- 
                                            背景
- This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.,CD59,16.3A5,1F5,EJ16,EJ30,EL32,G344,HRF-20,HRF20,MAC-IP,MACIF,MEM43,MIC11,MIN1,MIN2,MIN3,MIRL,MSK21,p18-20,Signal Transduction,Kinase,Tyrosine kinases,Immunology & Inflammation,CD markers,Cell Intrinsic Innate Immunity Signaling Pathway,Stem Cells,Hematopoietic Progenitors,Cardiovascular,CD59
- 
                                            分子量
- 14 kDa
- 
                                            基因ID
- 966
- 
                                            UniProt
- P13987
- 
                                            途径
- Complement System
 抗原
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