Rabbit Polyclonal Gliomedin antibody. Suitable for WB, ICC/IF and reacts with Mouse, Rat samples. Cited in 7 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
WB | ICC/IF | |
---|---|---|
Mouse | Tested | Expected |
Rat | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 10 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Ligand for NRCAM and NFASC/neurofascin that plays a role in the formation and maintenance of the nodes of Ranvier on myelinated axons. Mediates interaction between Schwann cell microvilli and axons via its interactions with NRCAM and NFASC (PubMed:16039564). Nodes of Ranvier contain clustered sodium channels that are crucial for the saltatory propagation of action potentials along myelinated axons. During development, nodes of Ranvier are formed by the fusion of two heminodes. Required for normal clustering of sodium channels at heminodes; not required for the formation of mature nodes with normal sodium channel clusters. Required, together with NRCAM, for maintaining NFASC and sodium channel clusters at mature nodes of Ranvier (By similarity).
Gliomedin, Gldn
Rabbit Polyclonal Gliomedin antibody. Suitable for WB, ICC/IF and reacts with Mouse, Rat samples. Cited in 7 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 98.98% PBS, 1% BSA
ab24483 detects a Gliomedin sized band at 70kDa in WB.
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Gliomedin also known by the alternate name Milk Fat Globule-EGF Factor 8 Protein or MFG-E8 plays an important role in the peripheral nervous system. It is a glycoprotein with a mass of approximately 40-50 kDa. Gliomedin expresses mainly at the node of Ranvier particularly in Schwann cells surrounding the peripheral nerves. This expression is key for maintaining proper function of myelinated nerves.
Gliomedin aids in the formation and maintenance of the nodes of Ranvier by interacting with proteins such as Neurofascin and NgCAM-related cell adhesion molecule (NrCAM). It is part of a complex which includes these proteins contributing to nodal organization and stability. Gliomedin anchors at the Schwann cell microvilli and connects with axonal cell adhesion molecules ensuring efficient signal transmission in nerve fibers.
Gliomedin interacts with cellular pathways responsible for nerve development and maintenance namely the axon guidance and myelin sheathing pathways. Its interaction with Neurofascin and NrCAM proteins facilitates proper node assembly and nerve signaling. These interactions are important to maintaining the fast conduction velocities required for signal transmission in the peripheral nervous system.
Alterations in gliomedin function relate to neuropathies and demyelinating diseases such as Guillain-Barré syndrome and Charcot-Marie-Tooth disease. Disruption of gliomedin interactions with Neurofascin and NrCAM can lead to compromised node integrity contributing to nerve conduction problems characteristic of these disorders. Understanding gliomedin's role may aid in developing therapeutic approaches targeting these conditions.
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ab24483 detects a band of 70 kDa in Western Blot. Gliomedin contains a number of N-glycosylation sites (SwissProt data) which may explain the migration at a higher molecular weight than predicted based on primary sequence.
All lanes: Western blot - Anti-Gliomedin antibody (ab24483) at 1 µg/mL
Lane 1: Mouse Sciatic Nerve Tissue Lysate at 10 µg
Lane 2: Rat Sciatic Nerve Tissue Lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG H&L (HRP) preadsorbed at 1/50000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 59 kDa
Observed band size: 70 kDa
Exposure time: 4min
ICC/IF image of ab24483 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab24483, 10μg/ml) overnight at +4°C. The secondary antibody (green) was Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899, DyLight® 488 goat anti-rabbit IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.
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