| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ABTB2-ATXN3-20-RERE | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-REOR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-REGO | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-REGR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-REAQ | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-ORRE | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-OROR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-ORGO | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-ORGR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-ORAQ | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GORE | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GOOR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GOGO | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GOGR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GOAQ | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GRRE | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GROR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GRGO | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GRGR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-GRAQ | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-AQRE | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-AQOR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-AQGO | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-AQGR | 20 (40 μL) | 200 μL |
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| ABTB2-ATXN3-20-AQAQ | 20 (40 μL) | 200 μL |
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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 12-44 to 52-86 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, Jul 2016]
Gene Symbol : ATXN3
Gene Name : Ataxin 3
Chromosome : CHR 14: 921,066,20-920,585,51
Locus : 14q32.12
Gene Symbol : ABTB2
Gene Name : Ankyrin repeat and BTB domain containing 2
Chromosome : CHR 11: 343,580,07-341,509,86
Locus : 11p13
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