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You are here:Home » Antibodies » Abs to Ataxin » Anti -ATXN3, ID (ATXN3, ATX3, MJD, MJD1, SCA3, Ataxin-3, Machado-Joseph disease protein 1, Spinocerebellar ataxia type 3 protein) (APC)

Anti -ATXN3, ID (ATXN3, ATX3, MJD, MJD1, SCA3, Ataxin-3, Machado-Joseph disease protein 1,
Spinocerebellar ataxia type 3 protein) (APC)

Pricing

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Specifications

Clone Host Grade Applications
Polyclonal Rabbit Affinity Purified E B IH FC
ATXN3 was known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein contains (CAG)n 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. There is a negative correlation between the age of onset and CAG repeat numbers.
Catalog #032319-APC
ApplicationsSuitable for use in Western Blot, Immunohistochemistry, Flow Cytometry, ELISA
Recommended DilutionELISA: 1:1,000
Western Blot: 1:100-500
Immunohistochemistry: 1:50-100
Flow Cytometry: 1:10-50
Storage and StabilityMay be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Do not freeze APC conjugates. Light sensitive. Aliquots are stable for 6 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Clone TypePolyclonal
IsotypeIgG
HostRabbit
SourceHuman
ConcentrationAs reported
FormSupplied as a liquid in PBS, pH 7.2. Contains ~0.09% sodium azide. Conjugated to Allophycocyanin (APC).
PurityPurified by Protein A affinity chromatography.
ImmunogenATXN3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 267~297 amino acids from the Center region of human ATXN3.
SpecificityHuman
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Alternate namesATXN3, ATX3, MJD, MJD1, SCA3, Ataxin-3, Machado-Joseph disease protein 1, Spinocerebellar ataxia type 3 protein


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