Validation Data Gallery
Tested Applications
| Positive WB detected in | HepG2 cells, A375 cells, L02 cells | 
Recommended dilution
| Application | Dilution | 
|---|---|
| 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. | |
Product Information
55301-1-AP targets FOXE3 in WB, ELISA applications and shows reactivity with human, mouse samples.
| Tested Reactivity | human, mouse | 
| Host / Isotype | Rabbit / IgG | 
| Class | Polyclonal | 
| Type | Antibody | 
| Immunogen | 
                                             Peptide 相同性解析による交差性が予測される生物種 | 
                                    
| Full Name | forkhead box E3 | 
| Calculated molecular weight | 33 kDa | 
| Observed molecular weight | 30-35 kDa | 
| GenBank accession number | NM_012186 | 
| Gene Symbol | FOXE3 | 
| Gene ID (NCBI) | 2301 | 
| RRID | AB_10896313 | 
| Conjugate | Unconjugated | 
| Form | |
| Form | Liquid | 
| Purification Method | Antigen affinity purification | 
| UNIPROT ID | Q13461 | 
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol{{ptg:BufferTemp}}7.3 | 
| Storage Conditions | Store at -20°C. Aliquoting is unnecessary for -20oC storage. | 
Background Information
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.
Protocols
| Product Specific Protocols | |
|---|---|
| WB protocol for FOXE3 antibody 55301-1-AP | Download protocol | 
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols | 




