Proteolipid Protein 1 (PLP1) (N-Term) Peptid

Details zu Produkt Nr. ABIN981869, Anbieter: Anmelden zum Anzeigen
Proteinname
  • GPM6C
  • HLD1
  • MMPL
  • PLP
  • PLP/DM20
  • PMD
  • SPG2
  • Plp
  • PLP1
  • plp1
  • DKFZp459O081
  • DKFZp459O113
  • DM20
  • jimpy
  • jp
  • msd
  • rsh
  • plp
  • hld1
  • mmpl
  • plp1a
  • pmd
  • spg2
  • DMalpha2c
  • wu:fc27f01
  • wu:fj36d03
  • wu:fj42d08
  • zgc:110499
  • proteolipid protein 1
  • proteolipid protein (myelin) 1
  • myelin proteolipid protein
  • proteolipid protein 1 L homeolog
  • proteolipid protein 1a
  • PLP1
  • Plp1
  • plp1
  • Tsp_11640
  • plp
  • plp1.L
  • plp1a
Protein Region
N-Term
Spezies
Human
3
2
2
2
2
2
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
Optionen
Hersteller
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Hersteller Produkt- Nr.
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Geblockter Antikörper anti-Proteolipid Protein 1 (PLP1) (N-Term) Antikörper (ABIN2778151)
Produktmerkmale This is a synthetic peptide designed for use in combination with anti-PLP1 antibody (Catalog #: ARP33843_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.
Reinigung Purified
Hintergrund 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.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: CALR,CANX,ITGAV,MAG,MBP,MBP

Protein Size: 277
Molekulargewicht 30 kDa
Gen-ID 5354
NCBI Accession NM_000533, NP_000524
UniProt P60201
Applikationshinweise Each Investigator should determine their own optimal working dilution for specific applications.
Beschränkungen Nur für Forschungszwecke einsetzbar
Format Lyophilized
Rekonstitution Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Konzentration 1 mg/mL
Buffer Final peptide concentration is 1 mg/mL in PBS.
Handhabung Avoid repeated freeze-thaw cycles.
Lagerung -20 °C
Informationen zur Lagerung For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.