This mouse monoclonal [4F11] antibody was generated against recombinant Survival Motor Neuron (SMN) protein and is specific for SMN exon 4 of human SMN.
Highlights:
The Survival motor neuron (SMN) protein complex is an essential component of the spliceosomal machinery. Defects in survival motor neuron protein 1 (SMN1), an intrigal component of the complex, lead to the autosomal recessive disorder, spinal muscular atrophy (SMA). Spinal muscular atrophy refers to a group of neuromuscular disorders characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy.
From the laboratory of Christian L. Lorson, PhD, University of Missouri - Columbia.
Part of The Investigator's Annexe program.
Product Type: | Antibody |
Antigen: | Survival Motor Neuron (SMN) |
Accession ID: | P97801 |
Molecular Weight: | 38 kDa |
Clonality: | Monoclonal |
Clone Name: | 4F11 |
Reactivity: | Human |
Immunogen: | Recombinant SMN protein |
Species Immunized: | Mouse |
Epitope: | SMN exon 4 |
Purification Method: | Protein G |
Buffer: | 0.1M Sodium Phosphate, pH 7.4, 0.15M NaCl, 0.05% (w/v) Sodium Azide |
Tested Applications: | WB: 1:1000; IF: 1:1000 |
Storage: | -20C |
Shipped: | Cold packs |
Epitope Mapping by Western Blot
GST-tagged SMN exons were individually expressed in bacterial cells. Immunoblots were performed against the GST tag, the blot was then stripped and reprobed with anti-SMN 4F11. The 4F11 maps to exon 4 of SMN.
Adapted from: Mattis V. et al., J Neurosci Methods. 2008 Oct 30;175(1):36-43.If you publish research with this product, please let us know so we can cite your paper.