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PLP1 antibody (Middle Region)

PLP1 Reactivity: Human, Rat, Mouse, Cow, Dog, Horse, Rabbit, Guinea Pig WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2778152
  • Target See all PLP1 Antibodies
    PLP1 (Proteolipid Protein 1 (PLP1))
    Binding Specificity
    • 16
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivity
    • 32
    • 24
    • 10
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Mouse, Cow, Dog, Horse, Rabbit, Guinea Pig
    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
    • 12
    • 9
    • 7
    • 7
    • 5
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    IYGTASFFFL YGALLLAEGF YTTGAVRQIF GDYKTTICGK GLSATVTGGQ
    Predicted Reactivity
    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%
    Characteristics
    This is a rabbit polyclonal antibody against PLP1. It was validated on Western Blot using a cell lysate as a positive control.
    Purification
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the middle region of human PLP1
    Top Product
    Discover our top product PLP1 Primary Antibody
  • Application Notes
    Optimal working dilutions should be determined experimentally by the investigator.
    Comment

    Antigen size: 277 AA

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    PLP1 (Proteolipid Protein 1 (PLP1))
    Alternative Name
    PLP1 (PLP1 Products)
    Synonyms
    GPM6C antibody, HLD1 antibody, MMPL antibody, PLP antibody, PLP/DM20 antibody, PMD antibody, SPG2 antibody, Plp antibody, PLP1 antibody, plp1 antibody, DKFZp459O081 antibody, DKFZp459O113 antibody, DM20 antibody, jimpy antibody, jp antibody, msd antibody, rsh antibody, plp antibody, hld1 antibody, mmpl antibody, plp1a antibody, pmd antibody, spg2 antibody, DMalpha2c antibody, wu:fc27f01 antibody, wu:fj36d03 antibody, wu:fj42d08 antibody, zgc:110499 antibody, PLP-B antibody, plp1-a antibody, plp1-b antibody, plp1b antibody, proteolipid protein 1 antibody, proteolipid protein (myelin) 1 antibody, myelin proteolipid protein antibody, proteolipid protein 1 L homeolog antibody, proteolipid protein 1a antibody, proteolipid protein 1 S homeolog antibody, PLP1 antibody, Plp1 antibody, plp1 antibody, Tsp_11640 antibody, plp antibody, plp1.L antibody, plp1a antibody, plp1.S antibody
    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.This gene encodes 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.
    Alias Symbols: MMPL, PLP, PLP/DM20, PMD, SPG2, HLD1
    Protein Interaction Partner: PTPRN, CLN8, Htt, ITGAV, ITGA5, MAG, MBP, CANX, CALR,
    Protein Size: 277
    Molecular Weight
    30 kDa
    Gene ID
    5354
    NCBI Accession
    NM_000533, NP_000524
    UniProt
    P60201
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