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Rabbit Polyclonal Antibody to FKTN
货号: P31160
别名: Fukutin, 2---, Fukuyama-type congenital muscular dystrophy protein, FKTN, FCMD
应用: WB,IHC
反应种属: Human
抗体类型: Primary antibody
Swissprot: O75072
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Description

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.

Specification

Aliases Fukutin, 2---, Fukuyama-type congenital muscular dystrophy protein, FKTN, FCMD
Entrez GeneID 2218
Swissprot O75072
WB Predicted band size 53.7kDa
Host/Isotype Rabbit IgG
Antibody Type Primary antibody
Storage Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity Human
Immunogen This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human FKTN.
Formulation Purified antibody in PBS with 0.05% sodium azide.

Application

WB 1/1000
IHC 1/100-1/500
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