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SCA7 is an autosomal dominant neurodegenerative disorder characterized by ataxia and selective neuronal cell loss caused by the expansion of a translated CAG repeat encoding a polyglutamine tract in ataxin-7
ApoER2 Monoclonal Antibody
When associated with LAPTM4B
Chromatin-modifying protein 1a
Ly6g Polyclonal Antibody - E-AB-70094 Size:200μL SCA7 is an autosomal dominantLy6g Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 70094 60, E AB 70094 120, E AB 70094 200 Citations, Manuals and MSDS Available upon request. Abbreviation: Ly6g Target Synonym: Gr 1; Gr1; Ly 6G. 1; Ly6G; Lymphocyte antigen 6 complex locus G; Lymphocyte antigen 6G Research Areas: Stem Cells,Tags and Cell Markers Conjugation: Unconjugated Host: Rabbit Species Reactivity: Mouse Application: IHC, IF Isotype: IgG Clonality:
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