- 中文名称
ATXN7多克隆抗体
- 英文名字
- ATXN7 Polyclonal Antibody
- 供应商
- Reddot Biotech
- 产品货号
- RD253584A
- 产品报价
- ¥询价/20uL ¥询价/60uL ¥询价/120uL ¥询价/200uL

- 产品说明书
- 点击查看
- 购买方式
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- 产品新闻

- 背景资料
- 该ATXN7 Polyclonal Antibody. 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. This locus has been mapped to chromosome 3, and it has been determined that the diseased allele associated with spinocerebellar ataxia-7 contains 38-130 CAG repeats (near the N-terminus), compared to 7-17 in the normal allele. The encoded protein is a component of the SPT3/TAF9/GCN5 acetyltransferase (STAGA) and TBP-free TAF-containing (TFTC) chromatin remodeling complexes, and it thus plays a role in transcriptional regulation. Alternative splicing results in multiple transcript variants.
- 应用类型
- IHC,ELISA
- 免疫原
- Synthetic peptide of human ATXN7
- 来源宿主
- 兔
- 反应性
- 人, 小鼠
- 保存建议
- 储存于-20 ℃。 避免冻融循环。
- 其他
- Reddot Biotech是由一支拥有35年医疗管理经验团队创办的加拿大本土品牌,其已在ELISA产品线上深耕7个年头,并且仍在不断前进中。产品的质量保证也让其越来越多被“收纳进”文献当中,产品线包括ELISA试剂盒、抗体、少量生化试剂,其中ELISA试剂盒超过6000+,物种类型较多:人;大鼠;小鼠;犬科类;牛科;鱼;鸡;猪;兔;山羊;绵羊;猿;马;豚鼠等,像激素类指标促卵泡素(FSH)、促黄体激素(LH),新冠相关病毒受体ACE2、ACE以及肿瘤免疫相关的指标精氨酸酶(ARG)等已是热门应用指标。

- 注意
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