Key Specifications Table
|Species Reactivity||Key Applications||Host||Format||Antibody Type|
|B, H, Po||IHC, IH(P)||M||Purified||Monoclonal Antibody|
|Presentation||Liquid. Immunoglobulin purified from ascites fluid.|
|Safety Information according to GHS|
|Storage and Shipping Information|
|Storage Conditions||Maintain at -20°C in undiluted aliquots for up to 12 months from date of receipt. Avoid repeated freeze/thaw cycles.|
|Material Size||60 µL|
Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3 SDS
|MOUSE ANTI-NEUROFILAMENT 70 HUMAN, BOVINE, PORCINE SPECIFIC MONOCLONAL ANTIBODY - 2328321||2328321|
|Reference overview||Application||Species||Pub Med ID|
|Neural progenitors from human embryonic stem cells.|
Reubinoff, B E, et al.
Nat. Biotechnol., 19: 1134-40 (2001) 2001
|Immunohistochemistry (Tissue)||Human Only||11731782|
|Long-term survival of fetal porcine lateral ganglionic eminence cells in the hippocampus of rats.|
Jacoby, D B, et al.
J. Neurosci. Res., 56: 581-94 (1999) 1999
Embryonic porcine brain tissue from the lateral ganglionic eminence was transplanted into the adult rat hippocampus to determine whether fetal striatal cells could survive, differentiate, and integrate in a heterotopic site. The hippocampus, a common site of epileptic seizure activity, was chosen to determine if fetal striatal cells could supply inhibitory GABAergic neurons that may serve to block seizures. Cells were either implanted with a single deposit using a standard metal cannula or by five smaller disseminated deposits with a glass micropipette. At 20-24 weeks, animals immunosuppressed with cyclosporin showed long-term survival of porcine cells in the adult hippocampus. Analysis by immunohistochemistry and in situ hybridization showed that the grafts contained glial and neuronal cell types, including GABAergic neurons within graft core and networks of porcine neuronal fibers extending from the graft into the host parenchyma. In addition, a marker of porcine presynaptic terminals, synaptobrevin, was abundant within the grafts and was found associated with hippocampal structures and cell layers suggesting functional integration of grafted cells within the host. The survival of xenografts in the hippocampus and potential integration of inhibitory components provides evidence that these grafts may serve as an internal negative feedback mechanism to quench epileptiform activity.