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Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) Peptide

PDSS1 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN938611

Quick Overview for Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) Peptide (ABIN938611)

Target

PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))

Origin

Mammalian

Source

  • 3
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Peptide Type

    Synthetic

    Sequence

    GEFLQLGSKE NENERFAHYL EKTFKKTASL IANSCKAVSV LGCPDPVVHE

    Characteristics

    A synthetic peptide for use as a blocking control in assays to test for specificity of PDSS1 antibody,
    Alternative Names: PDSS1 control peptide, PDSS1 antibody Blocking Peptide, Anti-PDSS1 Blocking Peptide, Prenyl decaprenyl diphosphate synthase subunit 1 Blocking Peptide, Decaprenyl Diphosphate Synthase Subunit 1 Blocking Peptide, COQ1 Blocking Peptide, MGC70953 Blocking Peptide, RP.3 Blocking Peptide, TPRT Blocking Peptide, TPT Blocking Peptide, hDPS1 Blocking Peptide, PDSS1, PDSS-1, PDSS 1, PDSS-1 Blocking Peptide, PDSS 1 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

    PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))

    Background

    PDSS1 is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. PDSS1 catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in PDSS1 gene are a cause of coenzyme Q10 deficiency.

    Molecular Weight

    46 kDa
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