Ataxin 3 anticorps (AA 120-250)
Aperçu rapide pour Ataxin 3 anticorps (AA 120-250) (ABIN6254159)
Antigène
Voir toutes Ataxin 3 (ATXN3) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 120-250
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Fonction
- Anti-ATXN3
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Séquence
- KEHWFTVRKL GKQWFNLNSL LTGPELISDT YLALFLAQLQ QEGYSIFVVK GDLPDCEADQ LLQMIRVQQM HRPKLIGEEL AQLKEQRVHK TDLERVLEAN DGSGMLDEDE EDLQRALALS RQEIDMEDEE ADL
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Specificité
- Detects levels of ATXN3 protein in transfected cells with GFP-ATXN3 and endogenous levels in U118, SH-SY5Y, At-T20 and hTERT cell lysates by Western blot. This Ab is similar to AB0089.
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Attributs du produit
- Ataxin 3
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Purification
- Epitope affinity purified
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Immunogène
- Purified recombinant peptide derived from within residues 120 aa to 250 aa of human ATXN3 produced in E. coli.
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Isotype
- IgG
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Indications d'application
- WB:1:250-1:2,000
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Restrictions
- For Research Use only
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Buffer
- preservatives. Glycerol and azide FREE.
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Agent conservateur
- Azide free
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Conseil sur la manipulation
- The antibody solution should be gently mixed before use.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For continuous use, store at 2-8 C for one-two days. For extended storage, store in -20 C freezer. Working dilution samples should be discarded if not used within 12 hours.
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- Ataxin 3 (ATXN3)
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Autre désignation
- ATXN3
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Sujet
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Goat polyclonal antibody to ATXN3. This protein appears to be a component of the ubiquitin proteasome system and has deubiquitinase activity. It may also have roles in neuroprotection, protein homeostasis maintenance, transcriptional and cytoskeleton regulation, myogenesis and degradation of misfolded chaperone substrates. The protein contains Qn repeats in the coding region, and the expansion of these repeats from the normal 13-36 to 68-79 is one cause of Machado-Joseph disease also known as spinocerebellar ataxia-3, an autosomal dominant neurologic disorder.
AT3, ATX3, ataxin-3, ataxin 3 variant h, autosomal dominant ataxin 3, ataxin 3 variant m, ataxin 3 variant ref, JOS, josephin, Machado-Joseph, Machado-Joseph disease protein 1, MJD, MJD1, SCA3, spinocerebellar ataxia 3, olivopontocerebellar ataxia 3, spinocerebellar ataxia type 3 protein antibody.
Antigène
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