FCMD polyclonal antibody (A01)

Catalog # H00002218-A01

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Size:50 uL
Price: USD $ 243.00
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  • +1-909-264-1399
    +1-909-992-0619
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  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

FCMD polyclonal antibody (A01), Lot # 051102JC01. Western Blot analysis of FCMD expression in human ovarian cancer.

QC Test

Western Blot detection against Immunogen (38.21 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant FCMD.

    Immunogen

    FCMD (NP_006722, 29 a.a. ~ 138 a.a) partial recombinant protein with GST tag.

    Sequence

    KHYLSTKNGAGLSKSKGSRIGFDSTQWRAVKKFIMLTSNQNVPVFLIDPLILELINKNFEQVKNTSHGSTSQCKFFCVPRDFTAFALQYHLWKNEEGWFRIAENMGFQCL

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (85); Rat (85)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (38.21 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Tissue lysate)

    FCMD polyclonal antibody (A01), Lot # 051102JC01. Western Blot analysis of FCMD expression in human ovarian cancer.

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — FKTN

    Entrez GeneID

    2218

    GeneBank Accession#

    NM_006731

    Protein Accession#

    NP_006722

    Gene Name

    FKTN

    Gene Alias

    CMD1X, FCMD, LGMD2M, MGC126857, MGC134944, MGC134945, MGC138243

    Gene Description

    fukutin

    Omim ID

    236670 253800 607440

    Gene Ontology

    Hyperlink

    Gene Summary

    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). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq

    Other Designations

    Fukuyama type congenital muscular dystrophy protein|OTTHUMP00000021841

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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