验证数据展示
经过测试的应用
Positive WB detected in | HepG2 cells, A375 cells, L02 cells |
推荐稀释比
应用 | 推荐稀释比 |
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Western Blot (WB) | WB : 1:500-1:1000 |
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
55301-1-AP targets FOXE3 in WB, ELISA applications and shows reactivity with human, mouse samples.
经测试应用 | WB, ELISA Application Description |
经测试反应性 | human, mouse |
免疫原 | Peptide 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 | forkhead box E3 |
别名 | ASMD, FKHL12, forkhead box E3, Forkhead box protein E3, FOXE3, FREAC 8, FREAC8 |
计算分子量 | 33 kDa |
观测分子量 | 30-35 kDa |
GenBank蛋白编号 | NM_012186 |
基因名称 | FOXE3 |
Gene ID (NCBI) | 2301 |
RRID | AB_10896313 |
偶联类型 | Unconjugated |
形式 | Liquid |
纯化方式 | Antigen affinity purification |
UNIPROT ID | Q13461 |
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. Aliquoting is unnecessary for -20oC storage. |
背景介绍
FOXE3, also named as FKHL12 and FREAC8, is a forkhead transcription factor expressed in the lens which is located at chromosome 1p32, have been associated with both recessive and dominant ocular disease. Defects in FOXE3 are a cause of anterior segment mesenchymal dysgenesis (ASMD). Defects in FOXE3 are a cause of congenital primary aphakia (CPA). This antibody is specific to FOXE3.
实验方案
Product Specific Protocols | |
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WB protocol for FOXE3 antibody 55301-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |