This is a synthetic peptide designed for use in combination with anti-ATN1 antibody (Catalog #: ARP34153_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Dentatorubral pallidoluysian atrophy is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion of a trinucleotide repeat within ATN1. The protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein.Dentatorubral pallidoluysian atrophy is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion of a trinucleotide repeat within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein.
Alias Symbols: B37, D12S755E, DRPLA, NOD, HRS
Protein Interaction Partner: ITCH,MAGI1,MAGI2,WWP1,WWP2,CASP1,CASP3,CASP7,CASP8,A2BP1,AES,AGRN,ARF3,ATN1,ATRX,BAIAP2,BAT2,BAT2L1,BAT3,CACNB1,CASP1,CASP3,CBFA2T2,CENPJ,CHRD,CRIP2,DMPK,DVL2,ECM1,EFCAB4B,EFEMP1,EFEMP2,EWSR1,FBLN1,FBLN2,FBLN5,GAPDH,GCC1,GIGYF1,GRN,HSPG2,ITCH,JAG2,KIAA0913,KRT31,KRTAP4-12,LENG8,LRP2,LTBP1,LTBP4,LYST,MAGI1,MAGI2,MAP7D1,MBP,MDFI,MEGF11,MEGF6,MEGF8,MYST2,MYST3,MYST4,NCK2,NELL1,NELL2,NOC2L,PCSK5,PDCD6IP,PFKL,PLSCR1,PSMA3,PSME3,RAD54L2,RBM10,RBM9,RBPMS,RCHY1,RERE,RHOXF2,RNF31,RUNX1T1,SIAH1,SIAH2,SLIT1,SPAG5,SSPO,STXBP4,SYVN1,TEP1,TLE1,TRIP6,USP54,VIM,WDR5,WWP1,WWP2,ZMYND8,BAIAP2,CTNND2,DVL1,ITCH,LYST,MAGI1,MAGI2,MYST2,RERE,TLE1,VIM,WWP1,WWP2