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The antibody detects endogenous levels of total SPTBN5 protein.
SPTBN5 (Spectrin Beta, Non-Erythrocytic 5) is a Protein Coding gene. Diseases associated with SPTBN5 include Epileptic Encephalopathy, Early Infantile, 5 and Spinocerebellar Ataxia 5. Among its related pathways are RET signaling and Signaling by GPCR. Gene Ontology (GO) annotations related to this gene include actin binding and kinesin binding. An important paralog of this gene is DST. [GeneCards]
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: beta V spectrin; Beta-V spectrin; HU HUSPECV; spectrin beta chain, brain 4; Spectrin beta chain, non-erythrocytic 5; spectrin, beta, non-erythrocytic 5; spectrin, non-erythroid beta chain 4
Gene Aliases: BSPECV; HUBSPECV; HUSPECV; SPTBN5
UniProt ID: (Human) Q9NRC6
Entrez Gene ID: (Human) 51332
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