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Asparagine-Linked Glycosylation 6, alpha-1,3-Glucosyltransferase Homolog (ALG6) Peptide

ALG6 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN936038
  • Target See all ALG6 products
    ALG6 (Asparagine-Linked Glycosylation 6, alpha-1,3-Glucosyltransferase Homolog (ALG6))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    YEAQRHWQEI TFNLPVKQWY FNSSDNNLQY WGLDYPPLTA YHSLLCAYVA
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of ALG6 antibody,
    Alternative Names: ALG6 control peptide, ALG6 antibody Blocking Peptide, Anti-ALG6 Blocking Peptide, Asparagine-Linked Glycosylation 6 Homolog Blocking Peptide, S. Cerevisiae Alpha-13-Glucosyltransferase Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    ALG6 (Asparagine-Linked Glycosylation 6, alpha-1,3-Glucosyltransferase Homolog (ALG6))
    Synonyms
    CG5091 Peptide, Dalg6 Peptide, Dmel\\CG5091 Peptide, alg6 Peptide, zgc:100813 Peptide, CDG1C Peptide, E230028F23Rik Peptide, garnysstan Peptide, asparagine-linked glycosylation 6 (alpha-1,3,-glucosyltransferase) Peptide, ALG6, alpha-1,3-glucosyltransferase Peptide, ALG6, alpha-1,3-glucosyltransferase S homeolog Peptide, gny Peptide, alg6 Peptide, ALG6 Peptide, alg6.S Peptide, Alg6 Peptide
    Background
    This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the first glucose residue to the growing lipid-linked oligosaccharide precursor of N-linked glycosylation. Mutations in this gene are associated with congenital disorders of glycosylation type Ic.
    Molecular Weight
    58 kDa
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