FKTN Polyclonal Antibody
Couldn't load pickup availability
Still have questions? Ask our experts!
FKTN Polyclonal Antibody
Â
| SKU # | E-AB-19886 |
| Reactivity | Human,  Mouse |
| Host | Rabbit |
| Applications | WB |
Â
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human,  Mouse |
| Applications | WB |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human FKTN |
| Abbre | FKTN |
| Synonyms | CMD1X,  FCMD,  FCMD gene,  FKTN,  Fukutin,  Fukuyama type congenital muscular dystrophy protein,  Fukuyama-type congenital muscular dystrophy protein,  LGMD2M,  MDDGA4,  MDDGB4,  MDDGC4,  MGC126857,  MGC134944,  MGC134945,  MGC138243,  OTTHUMP00000021841,  patient fukutin |
| Swissprot | |
| Calculated MW | 54 kDa |
| Observed MW | Refer to figures |
| Cellular Localization | Golgi apparatus membrane. |
| Concentration | 1.08 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Antigen affinity purification |
| Research Areas | Cancer,  Developmental biology,  Tags and Cell markers |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
Â
Related Reagents
| Applications | Recommended Dilution |
| WB | 1:500-1:2000 |
Â
Background Â
The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.