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PLP1 antibody

This Rabbit Polyclonal antibody specifically detects PLP1 in WB. It exhibits reactivity toward Human, Rat, Mouse and Dog.
Catalog No. ABIN635572
$1,297.32
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 9 to 12 Business Days

Quick Overview for PLP1 antibody (ABIN635572)

Target

See all PLP1 Antibodies
PLP1 (Proteolipid Protein 1 (PLP1))

Reactivity

  • 37
  • 29
  • 13
  • 10
  • 9
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse, Dog

Host

  • 38
  • 13
  • 3
Rabbit

Clonality

  • 42
  • 12
Polyclonal

Conjugate

  • 30
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PLP1 antibody is un-conjugated

Application

  • 43
  • 19
  • 17
  • 13
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  • 12
  • 11
  • 7
  • 7
  • 5
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Purification

    Affinity purified

    Immunogen

    PLP1 antibody was raised using a synthetic peptide corresponding to a region with amino acids GHEALTGTEKLIETYFSKNYQDYEYLINVIHAFQYVIYGTASFFFLYGAL
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    PLP1 Blocking Peptide, (ABIN938693), is also available for use as a blocking control in assays to test for specificity of this PLP1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PLP1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    PLP1 (Proteolipid Protein 1 (PLP1))

    Alternative Name

    PLP1

    Background

    PLP1 is a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene.

    Molecular Weight

    30 kDa (MW of target protein)
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