Proteolipid Protein 1 (PLP1) ELISA Kits

PLP1 encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. Zusätzlich bieten wir Ihnen Proteolipid Protein 1 Antikörper (47) und Proteolipid Protein 1 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
PLP1 18823 P60202
PLP1 5354 P60201
PLP1 24943 P60203
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Top Proteolipid Protein 1 ELISA Kits auf antikoerper-online.de

Showing 9 out of 20 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Human 0.056 ng/mL 0.15-10 ng/mL 96 Tests Anmelden zum Anzeigen 11 bis 15 Tage
533,33 €
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Human 0.072 ng/mL 0.15-10.0 ng/mL   96 Tests Anmelden zum Anzeigen 6 bis 8 Tage
679,90 €
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Ratte 78-5000 pg/mL   96 Tests Anmelden zum Anzeigen 6 bis 8 Tage
679,90 €
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Ratte 46.9 pg/mL 78-5000 pg/mL   96 Tests Anmelden zum Anzeigen 11 bis 15 Tage
452,57 €
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Maus 32.4 pg/mL 78.125-5000 pg/mL   96 Tests Anmelden zum Anzeigen 7 bis 14 Tage
707,14 €
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Schwein
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
945,85 €
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Rind (Kuh)
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
945,85 €
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Huhn
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
1.013,20 €
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Hund
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
1.013,20 €
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Am meisten referenzierte Proteolipid Protein 1 ELISA Kits

  1. Human PLP1 ELISA Kit für Sandwich ELISA - ABIN417339 : Miners, Palmer, Love: Pathophysiology of Hypoperfusion of the Precuneus in Early Alzheimer's Disease. in Brain pathology (Zurich, Switzerland) 2015 (PubMed)

Weitere ELISA Kits für Proteolipid Protein 1 Interaktionspartner

Mouse (Murine) Proteolipid Protein 1 (PLP1) Interaktionspartner

  1. axonal mitochondria, smooth endoplasmic reticulum, and microtubules were characterized in rodent optic nerves where PLP (zeige C3 ELISA Kits) is replaced by the peripheral nerve myelin protein, P0.

  2. The observations collectively support the idea that GST-pi (zeige GSTP1 ELISA Kits)(Nuc (zeige SREBF2 ELISA Kits))/DM-20 mRNA-expressing cells are the progeny of NG2 (zeige Vcan ELISA Kits)-positive OPCs rather than a novel type of oligodendrocyte-lineage progenitor cells and that DM-20 mRNA expression is dynamically regulated during differentiation of OPCs into oligodendrocytes.

  3. In the absence of P0, thus, PLP (zeige C3 ELISA Kits) also contributes to myelination by Schwann cells and to the preservation of peripheral axons

  4. while PLP (zeige C3 ELISA Kits) can co-exist with P0 in peripheral nervous system(PNS) myelin, PLP (zeige C3 ELISA Kits) cannot replace P0 as the major structural protein of PNS myelin.

  5. Both extracellular and intracellular epitopes of PLP (zeige C3 ELISA Kits) contribute to the pathogenesis of MP4-induced experimental autoimmune encephalomyelitis already in the setting of intact myelin.

  6. The insertion of native PLP (zeige C3 ELISA Kits) into Olg mitochondria of animals with PLP1/Plp1 regulates extracellular pH and adenosine triphosphate.

  7. This study shows for the first time that Plp (zeige C3 ELISA Kits)-null mice exhibit severe early-onset thermal hyperalgesia that is not associated with changes in thermal allodynic behavior.

  8. A novel mechanism sheds light on the immune regulation by which sulfatide-reactive type II natural killer (NK)T cells suppress inflammatory class II histocompatibility-restricted pathogenic CD4 (zeige CD4 ELISA Kits)+ T cell responses in a T cell-mediated autoimmune disease.

  9. that an early reactive glia response occurs following mutations in the PLP (zeige C3 ELISA Kits) gene

  10. Result suggest that plp1 plays a role either in the structural integrity of oligodendrocyte progenitor cell processes or in their response to extracellular cues that orient process outgrowth.

Human Proteolipid Protein 1 (PLP1) Interaktionspartner

  1. it seems that the epitopes of some microorganisms mimicking PLP such as PLP58-74 might have a potential role in the initiation of Multiple Sclerosis.

  2. Human induced pluripotent stem cells-derived oligodendrocytes from 12 individuals with Pelizaeus-Merzbacher and identified individual and shared defects in PLP1 mRNA expression and splicing, oligodendrocyte progenitor development, and oligodendrocyte morphology and capacity for myelination.

  3. report a novel mutation of the PLP1 gene in two siblings with Pelizaeus-Merzbacher disease associated with a rare and protean neuroimaging finding of optic nerve enlargement

  4. Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher disease. We identified PLP1 mutations in seven male patients with PMD.

  5. In major depressive disorder there was a significantly reduced expression of PLP1 mRNA.

  6. Study investigated 17 unrelated Pelizaeus-Merzbacher disease subjects with copy number gains at the PLP1 locus including triplication and quadruplication of specific genomic intervals-16/17 were found to have a duplication-inverted triplication-duplication rearrangement product.

  7. Myelin proteolipid protein is critical to regulating oligodendrocyte progenitor cell migration.

  8. PLP1 splicing mutations may result in a wide variety of disease phenotypes through a combination of multiple molecular pathogenic mechanisms.

  9. this study provides new insight into the genotype-phenotype correlations of patients with PLP1 splice-site mutations.

  10. Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease.

Proteolipid Protein 1 (PLP1) Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit Proteolipid Protein 1 (PLP1) ELISA Kits

  • proteolipid protein 1 (PLP1) Antikörper
  • proteolipid protein 1 (plp1) Antikörper
  • myelin proteolipid protein (Tsp_11640) Antikörper
  • myelin proteolipid protein (plp) Antikörper
  • proteolipid protein (myelin) 1 (Plp1) Antikörper
  • proteolipid protein 1 (Plp1) Antikörper
  • proteolipid protein 1 (plp1-a) Antikörper
  • DKFZp459O081 Antikörper
  • DKFZp459O113 Antikörper
  • DM20 Antikörper
  • GPM6C Antikörper
  • hld1 Antikörper
  • jimpy Antikörper
  • jp Antikörper
  • mmpl Antikörper
  • msd Antikörper
  • Plp Antikörper
  • PLP/DM20 Antikörper
  • plp1 Antikörper
  • plp1a Antikörper
  • pmd Antikörper
  • rsh Antikörper
  • spg2 Antikörper

Bezeichner auf Proteinebene für Proteolipid Protein 1 (PLP1) ELISA Kits

proteolipid protein 1 , proteolipid protein 1 (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated) , myelin proteolipid protein , lipophilin , myelin synthesis deficiency , rump shaker , major myelin proteolipid protein , Proteolipid protein (Pelizaeus-Merzbacher disease spastic paraplegia 2 uncomplicated) , Proteolipid protein (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated) , proteolipid protein (myelin) 1 , PLP , proteolipid protein, lipophilin , PLP-A , lipophilin-A , myelin proteolipid protein (PLP) , myelin proteolipid protein A , proteolipid protein 1 a

GENE ID SPEZIES
465785 Pan troglodytes
613099 Xenopus (Silurana) tropicalis
752012 Taeniopygia guttata
100173486 Pongo abelii
100174736 Pongo abelii
10903177 Trichinella spiralis
100136749 Oncorhynchus mykiss
18823 Mus musculus
5354 Homo sapiens
281410 Bos taurus
24943 Rattus norvegicus
396214 Gallus gallus
481002 Canis lupus familiaris
397029 Sus scrofa
100009169 Oryctolagus cuniculus
398334 Xenopus laevis
100220245 Taeniopygia guttata
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