-
Product Name
Anti-Myelin oligodendrocyte glycoprotein antibody
- Documents
-
Description
Rabbit polyclonal to Myelin oligodendrocyte glycoprotein
-
Tested applications
ELISA, WB, IHC-P
-
Species reactivity
Rat Myelin oligodendrocyte glycoprotein
-
Alternative names
BTN6 antibody; BTNL11 antibody; MOGIG2 antibody; NRCLP7 antibody; B230317G11Rik antibody; B230317G11Rik antibody; DAQB-92E24.2 antibody; MGC26137 antibody; Mog antibody; MOG antibody; MOGIG2 antibody
-
Isotype
Rabbit IgG
-
Preparation
Produced in rabbits immunized with purified, recombinant Rat Myelin oligodendrocyte glycoprotein (1PKQ_E; 1M-139H). Myelin oligodendrocyte glycoprotein specific IgG was purified by Rat Myelin oligodendrocyte glycoprotein affinity chromatography.
-
Clonality
Polyclonal
-
Formulation
0.2 μm filtered solution in PBS
-
Storage instructions
This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles. -
Applications
WB: 10-30 μg/ml
ELISA: 0.1-0.2 μg/mL
This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Rat Myelin oligodendrocyte glycoprotein. The detection limit for Rat Myelin oligodendrocyte glycoprotein is < 0.039 ng/well.
IHC-P: 0.1-1 μg/mL
-
Background
Myelin oligodendrocyte glycoprotein (MOG) is a transmembrane protein belonging to immunoglobulin superfamily, and contains an Ig-like domain followed by two potential membrane-spanning regions. MOG is expressed only in the CNS with very low content (approximately 0.1% total proteins) in oligodendrogliocyte membrane. Three possible functions for MOG were suggested: (a) a cellular adhesive molecule, (b) a regulator of oligodendrocyte microtubule stability, and (c) a mediator of interactions between myelin and the immune system, in particular, the complement cascade. A direct interaction might exist between the membrane-associated regions of MOG and the myelin-specific glycolipid galactocerebroside (Gal-C), and such an interaction may have important consequences regarding the membrane topology and function of both molecules. It is considered that MOG is an autoantigen capable to produce a demyelinating multiple sclerosis-like disease in experimental animals.
-
References
- Chekhonin VP, et al. (2003) Myelin oligodendrogliocyte glycoprotein: the structure, functions, role in pathogenesis of demyelinating disorders. Biomed Khim. 49(5): 411-23.
- Hilton AA, et al. (1995) Characterization of cDNA and Genomic Clones Encoding Human Myelin Oligodendrocyte Glycoprotein. J Neurochem. 65(1): 309-18.
- Johns TG, et al. (1999) The Structure and Function of Myelin Oligodendrocyte Glycoprotein. J Neurochem. 72(1): 1-9.
Related Products / Services
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"