![[KO]HPRT Rabbit mAb-抗体-威格顿生物](/uploads/20260414/ad4291519985458ac81d7dea66c4005d.png)
![[KO]HPRT Rabbit mAb](/assets/addons/ldcms/ldcms2025/images/product-default-flat.png)
Overview
| 别名 | HPRT1; HPRT; Hypoxanthine-guanine phosphoribosyltransferase; HGPRT; HGPRTase |
| 基因名 | HPRT1 |
| UniProt ID | P00492 |
| 反应种属 | Human,Mouse,Rat |
| 应用 | WB,IHC-P,IP |
| 宿主 | Rabbit |
| 偶联物 | Unconjugated |
| 修饰 | Unmodified |
| 亚型 | IgG |
| 克隆号 | R08-7C-3 |
| 克隆性 | Monoclonal Antibody |
| 分子量 | Calculated MW: 25 kDa; Observed MW: 25 kDa |
| 纯化方式 | Affinity Chromatography |
| 产品形式 | Liquid |
| 推荐稀释比 | WB-1:1000-1:5000; IHC-P-1:100-1:200; IP-1:10-1:100 |
| 存储缓冲液 | Liquid in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. |
| 保存温度 | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| 背景信息 | HPRT, also named HPRT1 and HGPRT, plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutation of HPRT1 is associated with Lesch-Nyhan syndrome (LNS) which is an X-linked inherited neurogenetic disorder of purine metabolism. It has been reported that HPRT1 also plays an important role in HPRT-related gout. |
检测原理