E-AB-19886
FKTN Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-19886
- Additional Names:
- 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
- Application:
- WB
- Concentration:
- 1.08 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Synthetic peptide of human FKTN
- Uniprot:
- O75072
- Synonyms:
- CMD1X;FCMD;fukutin;Fukuyama type congenital muscular dystrophy protein;Fukuyama-type congenital muscular dystrophy protein;LGMD2M;LGMDR13;MDDGA4;MDDGB4;MDDGC4;patient fukutin;ribitol-5-phosphate transferase
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice