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Anti-FKTN Antibody (R1E98)

Catalog #:   RHB07601 Specific References (11) DATASHEET
Host species: Rabbit
Isotype: IgG
Applications: IHC, WB
Accession: O75072
Overview

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

Data Image
  • Western blot
    Western blot analysis of Fukutin expression in HeLa cell lysate.
  • Western blot
    All lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
  • Western blot
    All lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
References

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

Datasheet

Document Download

Anti-FKTN Antibody (R1E98).pdf

 

$ 290
Product specifications
50 μg 290 100 μg 484

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For research use only. Not for human or drug use.

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Anti-FKTN Antibody (R1E98) [RHB07601]
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