OPLAH 抗体 (AA 1119-1288)
Quick Overview for OPLAH 抗体 (AA 1119-1288) (ABIN6145037)
抗原
See all OPLAH 抗体适用
宿主
克隆类型
标记
应用范围
- 
    - 
                                            抗原表位
- AA 1119-1288
- 
                                            序列
- TVAGGAGAGP SWHGRSGVHS HMTNTRITDP EILESRYPVI LRRFELRRGS GGRGRFRGGD GVTRELLFRE EALLSVLTER RAFRPYGLHG GEPGARGLNL LIRKNGRTVN LGGKTSVTVY PGDVFCLHTP GGGGYGDPED PAPPPGSPPQ ALAFPEHGSV YEYRRAQEAV
- 
                                            交叉反应
- 人, 小鼠, 大鼠
- 
                                            产品特性
- Polyclonal Antibodies
- 
                                            免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1119-1288 of human OPLAH (NP_060040.1).
- 
                                            亚型
- IgG
 
- 
                                            
- 
    
- 
    - 
                                            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.
 
- 
                                            
- 
    - OPLAH (5-Oxoprolinase (ATP-Hydrolysing) (OPLAH))
- 
                                            别名
- OPLAH
- 
                                            背景
- The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD).,OPLAH,5-Opase,OPLA,OPLAHD,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,OPLAH
- 
                                            分子量
- 137 kDa
- 
                                            基因ID
- 26873
- 
                                            UniProt
- O14841
 抗原
- 
                    
 
                                     
                                     
                                    