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 Predict reactive species |
| 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 | Liquid |
| Purification Method | Antigen affinity purification |
| UNIPROT ID | Q13461 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol, pH 7.3. |
| Storage Conditions | Store at -20°C. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
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 |









