Human Dynamin 1 Antibody from MYBIOSOURCE INC.
Search, find, compare suppliers for anti-Human Dynamin 1 antibody, protein, ELISA kits.
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| Antigenic Specificity | Human Dynamin 1 |
| Clone | polyclonal |
| Host Species | Rabbit |
| Reactive Species | human |
| Isotype | n/a |
| Format | DyLight 488 conjugate |
| Size | 0.1 mg |
| Concentration | n/a |
| Applications | Flow Cytometry (FC/FACS) |
| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
| Description | Specificity: No cross reactivity with other proteins. Dynamin-1 is a protein that in humans is encoded by the DNM1 gene. This gene encodes a member of the dynamin subfamily of GTP-binding proteins. The encoded protein possesses unique mechanochemical properties used to tubulate and sever membranes, and is involved in clathrin-mediated endocytosis and other vesicular trafficking processes. Actin and other cytoskeletal proteins act as binding partners for the encoded protein, which can also self-assemble leading to stimulation of GTPase activity. More than sixty highly conserved copies of the 3' region of this gene are found elsewhere in the genome, particularly on chromosomes Y and 15. Alternatively spliced transcript variants encoding diffe |
| Immunogen | Immunogen: E Coli-derived human Dynamin 1 recombinant protein (Position: W616-D667). |
| Other Names | [Rabbit IgG Human Dynamin 1 DyLight 488 Conjugated, Flow Validated; Dynamin-1; DNM1; DNM; Dynamin 1] |
| Gene, Accession # | [DNM1], Gene ID: 1759, NCBI: NP_001005336.1, UniProt: Q05193 |
| Catalog # | MBS1751424 |
| Price | $330 |
| Order / More Info | Human Dynamin 1 Antibody from MYBIOSOURCE INC. |
| Product Specific References | 1. Dhindsa, R. S., Bradrick, S. S., Yao, X., Heinzen, E. L., Petrovski, S., Krueger, B. J., Johnson, M. R., Frankel, W. N., Petrou, S., Boumil, R. M., Goldstein, D. B. Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis. Neurol. Genet. 1: e4, 2015. 2. EuroEPINOMICS-RES Consortium, Epilepsy Phenome/Genome Project, Epi4K Consortium. De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies. Am. J. Hum. Genet. 95: 360-370, 2014. |
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MYBIOSOURCE INC.
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