Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
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. Additionally we are shipping Myelin Basic Protein Kits (54) and Myelin Basic Protein Proteins (28) and many more products for this protein.
Showing 10 out of 186 products:
Human Polyclonal MBP Primary Antibody for ICC, IHC - ABIN1078364
Bleyer, Curths, Dahlmann, Wichmann, Bauer, Moritz, Braun, Knauf, Kaup, Gruber-Dujardin: Morphology and staining behavior of neutrophilic and eosinophilic granulocytes of the common marmoset (Callithrix jacchus). in Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie 2016
Rat (Rattus) Polyclonal MBP Primary Antibody for ELISA, WB - ABIN1574105
Kraitsy, Uecal, Grossauer, Bruckmann, Pfleger, Ropele, Fazekas, Gruenbacher, Patz, Absenger, Porubsky, Smolle-Juettner, Tezer, Molcanyi, Fasching, Schaefer: Repetitive long-term hyperbaric oxygen treatment (HBOT) administered after experimental traumatic brain injury in rats induces significant remyelination and a recovery of sensorimotor function. in PLoS ONE 2014
t-PA (show PLAT Antibodies) binds to Lys91 in the MBP (show MBL2 Antibodies) NH2-terminal region and PLG (show PLG Antibodies) binds to Lys122 in the MBP (show MBL2 Antibodies) COOH-terminal region. This proximity promotes the activation of PLG (show PLG Antibodies) by t-PA (show PLAT Antibodies).
Specific sites of post-translational modifications in multiple sclerosis patients are localized in two zones of MBP (show MBL2 Antibodies) 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 (show MBL2 Antibodies) 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 (show NDEL1 Antibodies)) mRNA levels in FEP patients compared with controls.
myelin basic protein has a role in activating CD4 (show CD4 Antibodies)+ and CD8 (show CD8A Antibodies)+ T lymphocytes in multiple sclerosis
B cells from relapsing-remitting multiple sclerosis patients produce TNFa (show TNF Antibodies) and IL6 (show IL6 Antibodies), and present MBP85-99 peptide
IL-17 (show IL17A Antibodies)- and IL-22 (show IL22 Antibodies)-secreting myelin specific CD4 (show CD4 Antibodies)(+) 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 (show CD4 Antibodies)+ T-cell autoreactivity in interferon-beta (show IFNB1 Antibodies)-treated multiple sclerosis patients may be mediated by monocyte-derived interleukin-10 (show IL10 Antibodies)
Concentrations of MBP did not increase after injury in all age groups
results provide a detailed picture of the MBP-CaM (show CALM PLURAL_@27095@) interaction, including a 3D model of the complex between full-length proteins
MBP-hydrolyzing antibodies may play an important role in multiple sclerosis pathogenesis
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 (show CDK7 Antibodies) activities.
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
results provide a detailed picture of the MBP-CaM (show KRIT1 PLURAL_@27095@) interaction, including a 3D model of the complex between full-length proteins
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 (show FOXP3 Antibodies) via nitric oxide in inducible nitric oxide synthase (show NOS2 Antibodies)-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 (show GSK3b Antibodies) and for the GSK-3beta (show GSK3b Antibodies)-mediated high phosphorylation of SH-binding proteins, including MBP and tau protein.
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 (show GAL Antibodies) 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 indicate a role for myelin basic protein (MBP) isoforms in protein-protein interactions during membrane and cytoskeletal extension and remodeling in oligodendrocytes (OLGs).
Disappearance of 21.5 pMBP (show PGRMC2 Antibodies) corresponded to demyelination and its reappearance corresponded to prevention of demyelination.
Golli-BG21 enhanced SCP1/GIP phosphatase activity, whereas PKCalpha (show PKCa Antibodies)-phosphorylated BG21 inhibited its activity, suggesting a potential role of BG21 as a molecular switch ("quick-brake mechanism") on SCP1/GIP.
Myelin basic protein cleaves cell adhesion molecule (show MCAM Antibodies) L1 and promotes neuritogenesis and cell survival.
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 basic protein
, myelin A1 protein
, myelin membrane encephalitogenic protein
, 20 kDa microtubule-stabilizing protein
, microtubule-stabilizing protein
, 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 deficient