库存-现货
瑞威尔生物科技 REVERE

Rabbit Polyclonal Antibody to ATXN1

现货 支持定制

  • 满200元免运费
  • 正品保障 提供发票
  • 现货闪电 当时发货

别名:ATX1; SCA1; D6S504E
应用:IHC
反应种属:Human, Mouse, Rat
规格:50μl/100μl

Description
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. 
Specification
Aliases ATX1; SCA1; D6S504E
Swissprot P54253
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, Mouse, Rat
Immunogen Fusion protein of human ATXN1
Formulation pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Application
IHC 1/50-1/200
ELISA 1/1000-1/5000

The image is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using P01115(ATXN1 Antibody) at dilution 1/40. (Original magnification: ×200)
The image is immunohistochemistry of paraffin-embedded Human brain tissue using P01115(ATXN1 Antibody) at dilution 1/40. (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。

暂无评论

发表回复

您的邮箱地址不会被公开。 必填项已用 * 标注


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。