FKTN Polyclonal Antibody
Code | Size | Price |
---|
E-AB-19886-20uL | 20uL | £125.00 |
Quantity:
E-AB-19886-60uL | 60uL | £172.00 |
Quantity:
E-AB-19886-120uL | 120uL | £237.00 |
Quantity:
E-AB-19886-200uL | 200uL | £344.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
- Human
- Mouse
Applications:
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Western Blot (WB)
Shipping:
Ice packs
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Images
Further Information
Abbreviation:
FKTN
Background:
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.
Buffer:
PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
Calculated MW:
54 kDa
Concentration:
1.08 mg/mL
Conjugation:
Unconjugated
Dilution:
WB 1:500-1:2000, ELISA 1:5000-1:10000
Immunogen:
Synthetic peptide of human FKTN
ObservedMW:
Refer to figures
Purification method:
Antigen affinity purification
Target Synonym:
CMD1X;FCMD;FCMD gene;FKTN;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
UNIProt ID:
O75072