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Antigenic Specificity | SPTAN1 |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | n/a |
Isotype | n/a |
Format | affinity purified |
Size | 0.1 mL |
Concentration | 100ug/100ul |
Applications | Immunofluorescence (IF), Western Blot (WB) |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | n/a |
Immunogen | Immunogen: The spectrin family of proteins were originally discovered as major components of the submembraneous cytoskeleton of osmotically lyzed red blood cells. The lyzed blood cells could be seen as clear red blood cell shaped objects in the light microscope and were referred to as red blood cell "ghosts". The major proteins of red blood cell ghosts proved to be actin, ankyrin, band 4.1 and several other proteins, including a closely spaced pair of bands running at about 240 and 260 |
Other Names | n/a |
Gene, Accession # | [SPTAN1] |
Catalog # | MBS416791 |
Price | $370 |
Order / More Info | SPTAN1 Antibody from MYBIOSOURCE INC. |
Product Specific References | 1. Marchesi VT & Steers E Jr. Selective solubilization of a protein component of the red cell membrane. Science 159:203-4 (1968).2. Levine J & Willard M. Fodrin: axonally transported polypeptides associated with the internal periphery of many cells. J Cell Biol. 90:631-42 (1981).3. Bennett V & Baines AJ. Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues. Physiol Rev. 81:1353-92 (2001).4. Djinovic-Carugo K, Gautel M, Yl nne J & Young P. The spectrin repeat: a structural platform for cytoskeletal protein assemblies. FEBS Lett. 513:119-23 (2002).5. Wang, DS and Shaw G. The association of the C-terminal region of beta I sigma II spectrin to brain membranes is mediated by a PH domain, does not require membrane proteins, and coincides with a inositol-1,4,5 triphosphate binding site. BBRC 217:608-15 (1995).6. Bennett V & Healy J. Organizing the fluid membrane bilayer: diseases linked to spectrin and ankyrin. Trends Mol Med 14:28-36 (2008).7. Eber S & Lux SE. Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin Hematol 41:118-41 (2004).8. Ikeda Y. et al. Spectrin mutations cause spinocerebellar ataxia type 5. Nature Genetics 38:184-90 (2006). |