Leinco Technologies

Anti-CNS Myelin/Oligodendrocytes

Product Code:
 
LEI-D103
Product Group:
 
Primary Antibodies
Host Type:
 
Mouse
Antibody Isotype:
 
IgM
Antibody Clonality:
 
Monoclonal
Antibody Clone:
 
CE1
Regulatory Status:
 
RUO
Target Species:
 
Human
Application:
 
Immunohistochemistry- Paraffin Embedded (IHC-P)
Shipping:
 
Ambient
Storage:
 
This purified antibody is stable when stored at 2-8°C. Do not freeze.
 

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CodeSizePrice
LEI-D103-0.125mg0.125 mg£444.00
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This product comes from: US.
Typical lead time: 14-21 working days.
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  • Further Information
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Further Information

Antigen Distribution:
The MOSP antigen is present on oligodendrocytes and CNS myelin but not on Schwann cells or peripheral nervous system (PNS) myelin. No specific staining is observed in sections from PNS, retina, liver, skin, or kidney.
Concentration:
0.5 mg/ml
Conjugate/Tag/Label:
Purified
Format:
This purified antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.4, 1% BSA and 0.09% sodium azide as a preservative.
Formulation:
This purified antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.4, 1% BSA and 0.09% sodium azide as a preservative.
Long Description:
Myelin is an electrically-insulating dielectric phospholipid layer that surrounds the axons of many neurons. It is an outgrowth glial cell: Schwann cells supply the myelin for peripheral neurons, whereas oligodendrocytes supply it to those of the central nervous system. Myelin is considered a defining characteristic of the (gnathostome) vertebrates, but it has also arisen by parallel evolution in some invertebrates. Myelin made by different cell types varies in chemical composition and configuration, but performs the same insulating function. Myelinated axons are white in appearance. Myelin is composed of about 80% lipid fat and about 20% protein. Some of the proteins that make up myelin are Myelin basic protein (MBP), Myelin oligodendrocyte glycoprotein (MOG), and Proteolipid protein (PLP).
Target:
Oligodendrocytes

References

1. Dyer, C. A. et al. (1991) J. of Neuroscience 28:607