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PLP1 antibody (AA 145-210)

This Rabbit Polyclonal antibody specifically detects PLP1 in WB, IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7269724

Quick Overview for PLP1 antibody (AA 145-210) (ABIN7269724)

Target

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

Reactivity

  • 33
  • 26
  • 11
  • 9
  • 9
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 36
  • 11
  • 3
Rabbit

Clonality

  • 40
  • 10
Polyclonal

Conjugate

  • 26
  • 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

  • 42
  • 19
  • 16
  • 13
  • 13
  • 11
  • 9
  • 7
  • 7
  • 6
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 16
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 145-210

    Purpose

    PLP1 Rabbit pAb

    Sequence

    TWTTCQSIAF PSKTSASIGS LCADARMYGV LPWNAFPGKV CGSNLLSICK TAEFQMTFHL FIAAFV

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 145-210 of human PLP1 (NP_955772.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    PLP1 (Proteolipid Protein 1 (PLP1))

    Alternative Name

    PLP1

    Background

    This gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein 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 Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants, including the DM20 splice variant.,PLP1,GPM6C,HLD1,MMPL,PLP,PLP/DM20,PMD,SPG2,Cell Biology & Developmental Biology,Cell Adhesion,Neuroscience,Cell Type Marker,Oligodendrocyte marker,PLP1

    Molecular Weight

    26kDa/30kDa

    Gene ID

    5354

    UniProt

    P60201
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