Ataxin 1 Recombinant Rabbit mAb - #BF3811

WB 1:1000-1:3000
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

Human, Mouse

Monoclonal [ReFirm23258]

Ataxin 1 Recombinant Rabbit mAb detects endogenous levels of Ataxin 1.

Unconjugated.

Affinity-chromatography.

Rabbit IgG in Tris-Glycine (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.

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 to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6,and it has been determined that the diseased allele contains 40-83 CAG repeats,compared to 6-39 in the normal allele,and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene.