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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) Peptide

MCAD Host: Synthetic BP, WB
Catalog No. ABIN8105037
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) Peptide (ABIN8105037)

Target

Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

Source

  • 6
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Purpose

    ACADM Peptide
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti-ACADM antibody ( ARP32788_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

    Background

    Background Information: ACADM Is the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Alternative Symbols: ACAD1, MCAD, MCADH

    Molecular Weight

    46kDa

    Gene ID

    34

    NCBI Accession

    NP_000007

    UniProt

    P11310
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