Atrophin 1 (ATN1) Peptide
ATN1
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all Atrophin 1 (ATN1) products
- Atrophin 1 (ATN1)
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-ATN1 antibody (Catalog #: ARP38087_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.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- Atrophin 1 (ATN1)
- Synonyms
- B37 Peptide, D12S755E Peptide, DRPLA Peptide, HRS Peptide, NOD Peptide, Atr1 Peptide, Drpla Peptide, atrophin-1 Peptide, RERE Peptide, ATN1 Peptide, atrophin 1 Peptide, ATN1 Peptide, Atn1 Peptide
- Background
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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
Protein Size: 1190 - Molecular Weight
- 125 kDa
- Gene ID
- 1822
- NCBI Accession
- NM_001940, NP_001931
- UniProt
- P54259
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