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WB analysis of human kidney lysate using GTX88124 LARGE (aa421-433) antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human kidney lysate using GTX88124 LARGE (aa421-433) antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human kidney lysate using GTX88124 LARGE (aa421-433) antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer

LARGE (aa421-433) antibody, Internal

GTX88124
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetLARGE1
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Overview

  • Supplier
    GeneTex
  • Product Name
    LARGE (aa421-433) antibody, Internal
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID9215
  • Target name
    LARGE1
  • Target description
    LARGE xylosyl- and glucuronyltransferase 1
  • Target synonyms
    acetylglucosaminyltransferase-like 1A; acetylglucosaminyltransferase-like protein; glycosyltransferase-like protein LARGE1; LARGE; LARGE xylosyl- and glucuronyltransferase 1; MDC1D; MDDGA6; MDDGB6
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO95461
  • Protein Name
    LARGE xylosyl- and glucuronyltransferase 1
  • Scientific Description
    This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203