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For maximum recovery of product, centrifuge the vial prior to removing the cap.
Sequence of this protein is as follows: ATTPSQRSQL EAYSTLLANM GSLSQAPGHK VEPP
Ataxin-1 (11NQ) refers to a specific isoform or variant of the Ataxin-1 protein, characterized by having 11 normal glutamine (Q) residues in its polyglutamine (polyQ) tract. This is in contrast to the expanded polyQ tracts found in disease-causing variants associated with spinocerebellar ataxia type 1 (SCA1). Ataxin-1 (11NQ) serves as a model for studying the normal physiological roles of Ataxin-1 and provides a contrast to the pathogenic forms associated with neurodegenerative diseases, enhancing our understanding of protein misfolding and aggregation disorders.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: alternative ataxin1; Ataxin-1; spinocerebellar ataxia 1; spinocerebellar ataxia 1 homolog; Spinocerebellar ataxia type 1 protein; Spinocerebellar ataxia type 1 protein homolog
Gene Aliases: 2900016G23Rik; ATX1; ATXN1; C85907; D6S504E; ENSMUSG00000074917; Gm10786; SCA1
UniProt ID: (Human) P54253, (Mouse) P54254, (Rat) Q63540
Entrez Gene ID: (Human) 6310, (Mouse) 20238, (Rat) 25049
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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