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Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads) Peptid

Acads Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN938486

Kurzübersicht für Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads) Peptid (ABIN938486)

Target

ACADS (Acads) (Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads))

Spezies

Säugetier

Quelle

  • 3
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    FTSGDKIGCF ALSEPGNGSD AGAASTTARA EGDSWVLNGT KAWITNAWEA

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of ACADS antibody,
    Alternative Names: ACADS control peptide, ACADS antibody Blocking Peptide, Anti-ACADS Blocking Peptide, Acyl-Coenzyme A Dehydrogenase C-2 To C-3 Short Chain Blocking Peptide, ACAD3 Blocking Peptide, SCAD Blocking Peptide
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

    ACADS (Acads) (Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads))

    Hintergrund

    ACADS is a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency.

    Molekulargewicht

    42 kDa
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