Comparison

ATN1 Peptide (AAP34153)

€151.00
Excl. VAT
Item no. AAP34153
Manufacturer AVIVA Systems Biology
Amount 100 ug
Category
Type Peptides
Format Lyophilized powder
Protein Family ITCH,MAGI1,MAGI2,WWP1,WWP2
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias B37, D12S755E, DRPLA, NOD
Available
Description
This is a synthetic peptide designed for use in combination with anti-ATN1 antibody (Catalog #: ARP34153_P050) made by Aviva Systems Biology. 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. Please inquire for more details.
Gene symbol
ATN1
Protein size
1190
Molecular weight
125kDa
Product format
Lyophilized powder
Gene id
1822
Reconstitution and storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Partner proteins
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
Description of target
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.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ug
Available: In stock
Listprice: €151.00
Price: €151.00
available

Delivery expected until 8/14/2025 

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