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The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann cells in the nervous system. Zusätzlich bieten wir Ihnen Myelin Basic Protein Antikörper (184) und Myelin Basic Protein Proteine (29) und viele weitere Produktgruppen zu diesem Protein an.
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Human MBP ELISA Kit für Sandwich ELISA - ABIN366557
Duan, Luo, Hao, Feng, Zhang, Lu, Xing, Feng, Yang, Song, Yan: Soluble CD146 in cerebrospinal fluid of active multiple sclerosis. in Neuroscience 2013
Human MBP ELISA Kit für Sandwich ELISA - ABIN366558
Ding, Zeng, Sroussi, Yu, Xu, Cheng, Fan: Interactions between Golli-MBP and Th1/Th2 cytokines in patients with oral lichen planus. in Oral diseases 2014
t-PA (zeige PLAT ELISA Kits) binds to Lys91 in the MBP (zeige MBL2 ELISA Kits) NH2-terminal region and PLG (zeige PLG ELISA Kits) binds to Lys122 in the MBP (zeige MBL2 ELISA Kits) COOH-terminal region. This proximity promotes the activation of PLG (zeige PLG ELISA Kits) by t-PA (zeige PLAT ELISA Kits).
Specific sites of post-translational modifications in multiple sclerosis patients are localized in two zones of MBP (zeige MBL2 ELISA Kits) suggests that these regions may be involved in antigen recognition by the body's immune surveillance machinery
Results provide novel insights into the role of genetic variation within the MBP (zeige MBL2 ELISA Kits) gene predicting multiple sclerosis clinical course, both directly and by interaction with known environmental MS risk factors
Deimination of myelin basic protein (MBP) by peptidylarginine deiminase (PAD) prevents its binding to the proteasome and decelerates its degradation by the proteasome in mammalian cells. Potential anticancer drug tetrazole analogue of chloramidine 2, at concentrations greater than 1 microM inhibits the enzymatic activity of PAD in vitro.
This study observed a significantly increased myelin basic protein (MBP) and nuclear distribution protein nudE-like 1 (NDEL1 (zeige NDEL1 ELISA Kits)) mRNA levels in FEP patients compared with controls.
myelin basic protein has a role in activating CD4 (zeige CD4 ELISA Kits)+ and CD8 (zeige CD8A ELISA Kits)+ T lymphocytes in multiple sclerosis
B cells from relapsing-remitting multiple sclerosis patients produce TNFa (zeige TNF ELISA Kits) and IL6 (zeige IL6 ELISA Kits), and present MBP85-99 peptide
IL-17 (zeige IL17A ELISA Kits)- and IL-22 (zeige IL22 ELISA Kits)-secreting myelin specific CD4 (zeige CD4 ELISA Kits)(+) T cells resistant to corticoids are associated with radiological activity of multiple sclerosis in early stages of the disease, mainly among Afrodescendant patients who, normally, have worse prognosis.
Studies indicate that all myelin basic protein (MBP) isoforms are intrinsically disordered proteins (IDPs) that interact via molecular recognition fragments (MoRFs), which thereby undergo local disorder-to-order transitions.
Reduced myelin basic protein-induced CD4 (zeige CD4 ELISA Kits)+ T-cell autoreactivity in interferon-beta (zeige IFNB1 ELISA Kits)-treated multiple sclerosis patients may be mediated by monocyte-derived interleukin-10 (zeige IL10 ELISA Kits)
The Mbp(+/-) mice exhibited defects of sensorimotor gating, as evidenced by reduced prepulse-inhibition, and a late-onset catatonia phenotype.
The present study provides evidence for a novel L1-mediated function of MBP in the developing spinal cord and in the injured adult mammalian nervous system that leads to enhanced recovery after acute trauma.
myelin basic protein (MBP) is inhibitory to both primitive neural stem cells and definitive neural stem cells derived colony formation.
CNP (zeige CNP ELISA Kits) directly associates with and organizes the actin cytoskeleton, thereby providing an intracellular strut that counteracts membrane compaction by myelin basic protein (MBP).
to further characterize the mechanism regulating mbp transcription, study defined M3 structure/function relationships; multiple M3 regulatory element combinations were found to drive expression in oligodendrocytes and Schwann cells with a minimal 129 bp sequence conferring expression in oligodendrocytes throughout myelin elaboration, maintenance and repair
Results show the expression of sncRNA715 in Schwann cells and its inverse correlation with Mbp mRNA in cultured cells and the sciatic nerve. Its inhibitory effect on MBP was confirmed in differentiating primary Schwann cells.
Results suggest that GAL (zeige GAL ELISA Kits) is a regulator of myelination, as demonstrated by MBP synthesis, and may be one of the myelination promoters
Data indicate that 18.5 kDa myelin basic protein (MBP) segment upstream of the primary SH3-ligand is involved in interaction.
Data suggest that prenatal alterations in expression of various fetal brain proteins (including up-regulation of Mbp) are associated with aberrant behavioral characteristics of transgenic mice that model autism-like behavior.
Data suggest that hybrid protein composed of two different Myelin basic protein (MBP) isoforms (TandeMBP) might become a tool for in vitro assays to analyse various protein kinase (zeige CDK7 ELISA Kits) activities.
Concentrations of MBP did not increase after injury in all age groups
results provide a detailed picture of the MBP-CaM interaction, including a 3D model of the complex between full-length proteins
MBP-hydrolyzing antibodies may play an important role in multiple sclerosis pathogenesis
trehalose completely avoid autocatalytic cleavage properties of MBP up to 4 days of incubation at 37 degrees C and pH 7.4.
formation of an imine between inflammatory-derived aldehydes can lead to structural changes in MBP and a decrease in myelin stability
MBP can induce a dihydrocholesterol-dependent segregation of phases that can be further regulated by the electrolyte concentration in the subphase and the composition (type and proportion) of non-sterol lipids.
Bovine MBP priming reduces expression of Foxp3 (zeige FOXP3 ELISA Kits) via nitric oxide in inducible nitric oxide synthase (zeige NOS2 ELISA Kits)-deficient mouse T cells.
investigation of bovine myelin basic protein binding to triphosphoinositide
There is a developmental regulation of posttranslationally modified forms of myelin basic protein into specific membrane microdomains.
These results suggest that phospholipids and sulfatide and heparin may function as effective stimulators for autophosphorylation of GSK-3beta (zeige GSK3b ELISA Kits) and for the GSK-3beta (zeige GSK3b ELISA Kits)-mediated high phosphorylation of SH-binding proteins, including MBP and tau protein.
The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann cells in the nervous system. However, MBP-related transcripts are also present in the bone marrow and the immune system. These mRNAs arise from the long MBP gene (otherwise called 'Golli-MBP') that contains 3 additional exons located upstream of the classic MBP exons. Alternative splicing from the Golli and the MBP transcription start sites gives rise to 2 sets of MBP-related transcripts and gene products. The Golli mRNAs contain 3 exons unique to Golli-MBP, spliced in-frame to 1 or more MBP exons. They encode hybrid proteins that have N-terminal Golli aa sequence linked to MBP aa sequence. The second family of transcripts contain only MBP exons and produce the well characterized myelin basic proteins. This complex gene structure is conserved among species suggesting that the MBP transcription unit is an integral part of the Golli transcription unit and that this arrangement is important for the function and/or regulation of these genes.
myelin A1 protein
, myelin membrane encephalitogenic protein
, myelin deficient
, Golli-Mbp; myelin basic protein
, Golli-Mbp; myelin basic protein; myelin basic protein S
, MBP S
, myelin basic protein Golli-mbp
, myelin basic protein S
, myelin basic protein
, 20 kDa microtubule-stabilizing protein
, microtubule-stabilizing protein