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ATN1 Peptide (AAP38087)

151,00 €
Zzgl. MwSt.
ArtNr AAP38087
Hersteller AVIVA Systems Biology
Menge 100 ug
Kategorie
Typ Peptides
Format Lyophilized powder
Protein Familie ITCH,MAGI1,MAGI2,WWP1,WWP2
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias B37, D12S755E, DRPLA, NOD
Lieferbar
Description
This is a synthetic peptide designed for use in combination with anti-ATN1 antibody (Catalog #: ARP38087_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.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ug
Lieferbar: In stock
Listenpreis: 151,00 €
Preis: 151,00 €
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Lieferung vsl. bis 14.08.2025 

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