Ataxin-1 (phospho Ser776) rabbit pAb
Rif. EK-ES7119
| 50µl | 188,00 € | ||
| 100µl | 316,00 € |
Informazioni sul prodotto
- ATXN1; ATX1; SCA1; Ataxin-1; Spinocerebellar ataxia type 1 protein
ataxin 1(ATXN1) Homo sapiens The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the 'pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted
Proprietà chimiche
Richiesta tecnica su: EK-ES7119 Ataxin-1 (phospho Ser776) rabbit pAb
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