验证数据展示
经过测试的应用
| Positive WB detected in | PC-3 cells, mouse testis tissue, rat testis tissue |
| Positive IP detected in | mouse testis tissue |
推荐稀释比
| 应用 | 推荐稀释比 |
|---|---|
| Western Blot (WB) | WB : 1:500-1:1000 |
| Immunoprecipitation (IP) | IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate |
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, Check data in validation data gallery. | |
产品信息
12020-1-AP targets SPATA7 in WB, IP, IF, IHC, ELISA applications and shows reactivity with human, mouse, rat samples.
| 经测试应用 | WB, IP, ELISA Application Description |
| 文献引用应用 | WB, IF, IHC |
| 经测试反应性 | human, mouse, rat |
| 文献引用反应性 | mouse |
| 免疫原 | SPATA7 fusion protein Ag2649 种属同源性预测 |
| 宿主/亚型 | Rabbit / IgG |
| 抗体类别 | Polyclonal |
| 产品类型 | Antibody |
| 全称 | spermatogenesis associated 7 |
| 别名 | HSD 3.1, HSD3, SPATA7, spermatogenesis associated 7 |
| 计算分子量 | 599 aa, 68 kDa |
| 观测分子量 | 68-80 kDa |
| GenBank蛋白编号 | BC008656 |
| 基因名称 | SPATA7 |
| Gene ID (NCBI) | 55812 |
| RRID | AB_2195380 |
| 偶联类型 | Unconjugated |
| 形式 | Liquid |
| 纯化方式 | Antigen affinity purification |
| UNIPROT ID | Q9P0W8 |
| 储存缓冲液 | PBS with 0.02% sodium azide and 50% glycerol , pH 7.3 |
| 储存条件 | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
SPATA7, also named as HSD3, may be involved in retinal function. It is interesting to note that mutations in SPATA7 cause LCA and RP/ARRP , two overlapping but distinct human retinal diseases. SPATA7 is another LCA and Juvenile RP Gene.(PMID:19268277) It is a highly conserved, vertebrate-specific protein which expressed in the mature retina. For some modification, the MW always migrate 5-8kd. The antibody can reoginze all the 3 isoforms of SPATA7.
实验方案
| Product Specific Protocols | |
|---|---|
| WB protocol for SPATA7 antibody 12020-1-AP | Download protocol |
| IP protocol for SPATA7 antibody 12020-1-AP | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |
发表文章
| Species | Application | Title |
|---|---|---|
Am J Hum Genet Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. | ||
Hum Mol Genet Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina.
| ||
Gene Ther AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa.
| ||
Exp Eye Res Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. |