Catalog No.
RHB07601
Species reactivity
Human, Mouse, Rat
Host species
Rabbit
Isotype
IgG
Clonality
Monoclonal
Tested applications
IHC: 1:100-1:200, WB: 1:1000-1:2000
Target
FCMD, Ribitol-5-phosphate transferase, FKTN, Fukutin, Fukuyama-type congenital muscular dystrophy protein
Concentration
1 mg/ml
Endotoxin level
Please contact with the lab for this information.
Purity
>95% by SDS-PAGE.
Purification
Protein A/G purified from cell culture supernatant.
Accession
O75072
Applications
IHC, WB
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4, 0.05% BSA, 50% Glycerol, 0.05% Sodium azide.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 4 ℃ for frequent use. Store at -20 ℃ for twelve months from the date of receipt.
Clone ID
R1E98
Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies., PMID:35302338
Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement., PMID:25821721
Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients., PMID:25814170
Detection of the dystroglycanopathy protein, fukutin, using a new panel of site-specific monoclonal antibodies., PMID:22771323
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency., PMID:21926082
Characteristics of neurons and glia in the brain of Fukuyama type congenital muscular dystrophy., PMID:19108571
Diagnosis and etiology of congenital muscular dystrophy., PMID:18160674
Intracellular binding of fukutin and alpha-dystroglycan: relation to glycosylation of alpha-dystroglycan., PMID:17005282
Identification of a functional CRE in the promoter of Fukuyama congenital muscular dystrophy gene fukutin., PMID:15893581
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients., PMID:12467726
Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain., PMID:10852541
For research use only. Not for human or drug use.
