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Rabbit
Anti-Ataxin 3/Gold
Cat. Number:
bs-17208R-Gold
Quantity size:
100ul
15nm
Concentration:
0.4mg/ml Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Background:
Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by this gene 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. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Sep 2009]
Also known as:
AT3;
Ataxin 3;
Ataxin-3;
ATX3;
ATX3_HUMAN;
ATXN3;
EC 3.4.22.;
JOS;
Josephin;
Machado Joseph disease (spinocerebellar ataxia 3, olivopontocerebellar ataxia 3, autosomal dominant, ataxin 3);
Machado Joseph disease;
Machado Joseph disease protein 1;
Machado-Joseph disease protein 1;
Machado-Joseph disease protein 1 homolog;
MJD;
MJD gene;
MJD1;
Olivopontocerebellar ataxia 3;
OTTHUMP00000221583;
OTTHUMP00000221585;
OTTHUMP00000221586;
OTTHUMP00000221587;
OTTHUMP00000231995;
OTTHUMP00000231997;
Rsca3;
SCA3;
SCA3 gene;
Spinocerebellar ataxia type 3 protein.
Specificity:
●
Rabbit Polyclonal IgG, affinity purified by Protein A.
●
Reacts with:
(predicted: )
●
Immunogen: KLH conjugated synthetic peptide derived from human Ataxin 3.
●
Predicted Molecular Weight: 42kDa.
Storage:
0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
Application:
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.