别名:AT3; JOS; MJD; ATX3; MJD1; SCA3应用:IHC
反应种属:Human
规格:50μl/100μl
| Description |
|---|
| 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. |
| Specification | |
|---|---|
| Aliases | AT3; JOS; MJD; ATX3; MJD1; SCA3 |
| Swissprot | P54252 |
| Host/Isotype | Rabbit IgG |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human |
| Immunogen | Fusion protein of human ATXN3 |
| Formulation | pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Application | |
|---|---|
| IHC | 1/50-1/300 |
| ELISA | 1/5000-1/10000 |
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The image is immunohistochemistry of paraffin-embedded Human liver cancer tissue using P09339(ATXN3 Antibody) at dilution 1/100. (Original magnification: ×200) |
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The image is immunohistochemistry of paraffin-embedded Human esophagus cancer tissue using P09339(ATXN3 Antibody) at dilution 1/100. (Original magnification: ×200) |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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