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Mouse OMgp Affinity Purified Polyclonal Ab (25 UG)

货号: AF1674-SP 基本售价: 1378.1 元 规格: -

产品信息

概述
货号AF1674-SP
别名oligodendrocyte myelin glycoprotein; OMG; OMGPoligodendrocyte-myelin glycoprotein
全称Oligodendrocyte-Myelin glycoprotein
反应种属Mouse
应用Western Blot(0.1 µg/mL)
目标/特异性Detects mouse OMgp in direct ELISAs and Western blots. In these formats, approximately 35% cross‑reactivity with recombinant human OMgp is observed.
使用方法Western Blot: 0.1 µg/mL
来源Reconstitute at 0.2 mg/mL in sterile PBS.
产品组分
性能
供应商R&D Systems
Entrez Gene IDs4974 (Human); 18377 (Mouse)
应用文献
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

Oligodendrocyte-myelin glycoprotein and Nogo negatively regulate activity-dependent synaptic plasticity.
Authors: Raiker SJ, Lee H, Baldwin KT
J. Neurosci., 2010;30(37):12432-45.
Species: Mouse
Sample Type: Tissue Homogenates
Application: WB
Oligodendrocyte myelin glycoprotein does not influence node of ranvier structure or assembly.
Authors: Chang KJ, Susuki K, Dours-Zimmermann MT
J. Neurosci., 2010;30(43):14476-81.
Species: Mouse
Sample Type: recombinant OMgp
Application: DB
Soluble Nogo receptor down-regulates expression of neuronal Nogo-A to enhance axonal regeneration.
Authors: Peng X, Zhou Z, Hu J, Fink DJ, Mata M
J. Biol. Chem., 2010;285(4):2783-95.
Species: Rat
Sample Type: Cell Lysates
Application: WB
Molecular basis of the interactions of the Nogo-66 receptor and its homolog NgR2 with myelin-associated glycoprotein: development of NgROMNI-Fc, a novel antagonist of CNS myelin inhibition.
Authors: Robak LA, Venkatesh K, Lee H, Raiker SJ, Duan Y, Lee-Osbourne J, Hofer T, Mage RG, Rader C, Giger RJ
J. Neurosci., 2009;29(18):5768-83.
Species: Rat
Sample Type: Tissue Homogenates
Application: WB
Reassessment of corticospinal tract regeneration in Nogo-deficient mice.
Authors: Lee JK, Chan AF, Luu SM, Zhu Y, Ho C, Tessier-Lavigne M, Zheng B
J. Neurosci., 2009;29(27):8649-54.
Species: Mouse
Sample Type: Tissue Homogenates
Application: WB

纯化方式Antigen Affinity-purified
免疫原Mouse myeloma cell line NS0-derived recombinant mouse OMgp (R&D Systems, Catalog # 1674-MG)
Ile25-Ser420
Accession # Q63912
生物活性Mouse
标记Unconjugated
溶解方法Reconstitute at 0.2 mg/mL in sterile PBS.
背景

Oligodendrocyte myelin glycoprotein (OMgp or OMG), Nogo, and myelin-associated glycoprotein (MAG), are three myelin-derived axon outgrowth inhibitors that collapse axonal growth cones and inhibit neurite outgrowth (1 - 3). These three structurally distinct proteins contribute to the myelin-associated inhibitory activity that prevents axonal regeneration after injury of the adult central nervous system (CNS). Mouse OMgp cDNA encodes a 440 amino acid (aa) residue glycosylphosphatidylinositol (GPI)-anchored protein that has a 24 aa signal peptide, eight leucine-rich repeats (LRR) followed by five serine/threonine-rich repeats (4). OMgp has multiple potential N-glycosylation and O-glycosylation sites. Mouse and human OMgp share approximately 88% aa sequence identity. OMgp is expressed on the surface of oligodendrocytes and on large projection neurons, including Purkinje cells of the cerebellum, pyramidal cells of the hippocampus, motoneurons of the brainstem and anterior horn cells of the spinal cord (5). The neurite outgrowth inhibitory activities of all three myelin-derived proteins are mediated by binding to a common receptor complex consisting of the Nogo receptor (NgR) and the p75 neurotrophin receptor (NGFR) (2, 3). Besides its function in the inhibition of axonal growth, OMgp has also been implicated in the inhibition of proliferation. Although the transmembrane receptor that mediates the proliferation inhibition activity has not been identified, the LRR repeats of OMgp were shown to be essential for both the proliferation inhibition and neurite outgrowth inhibition activities (6).

运输条件Blue Ice
存放说明4℃
参考文献
  1. Kottis, V. et al. (2002) J. Neurochem. 82:1566.
  2. Wang, K. et al. (2002) Nature 417:941.
  3. Wang, K. et al. (2002) Nature 420:74.
  4. Mikol, D.D. et al. (1993) Genomics 17:604.
  5. Habib, A. et al. (1998) J. Neurochem. 70:1704.
  6. Vourc’h, P. et al. (2003) J. Neurochem. 85:889.