产品货号：
Z30673
中文名称：
PEX5抗体
英文名称：
Anti-PEX5 Antibody
产品规格：
100μl
发货周期：
1～3天
产品价格：
询价
| 抗体名称 | Anti-PEX5 Antibody |
| 指标别名 | Peroxin 5;Peroxisome Marker;Peroxisome receptor 1;PEX5;PTS1 BP;PTS1 receptor;PTS1R;PXR1 |
| 克隆性 | Polyclonal |
| 检验物种 | human,mouse |
| 应用范围 | WB |
| 基因名称 | PEX5 |
| 抗体来源 | Rabbit |
| 抗体类型 | IgG |
| 免疫原 | Synthesized peptide derived from the C-terminal region of human Peroxin 5.at AA rangle:540-620 |
| 计算分子量 | 71KD |
| 成分 | Liquid in PBS containing 50% glycerol,0.5% BSA and 0.02% sodium azide. |
| 纯化方式 | Immunogen affinity purified |
| 产品形态 | 溶液 |
| 保存条件 | -20℃可保存1年，短期保存或频繁使用请置于4℃，可保存一个月，避免反复冻融。 |
| 背景资料 | The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import.Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes.The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive,lethal diseases characterized by multiple defects in peroxisome function.The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups.Although the clinical features of PBD patients vary,cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle.Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD),a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD).Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq] |
| Uniprot ID | P50542 |
| 基因名全称 | Peroxisomal targeting signal 1 receptor |
| 推荐稀释比 | WB,1:500～1:2000 |
相关搜索：PEX5抗体，PEX5多抗，Anti-PEX5 Antibody