ATX7 rabbit pAb
- 公司名稱 上海貝博生物科技有限公司
- 品牌
- 型號
- 產地
- 廠商性質 生產廠家
- 更新時間 2025/7/13 21:57:30
- 訪問次數 37
聯系方式：張經理18930271235 查看聯系方式
聯系我們時請說明是化工儀器網上看到的信息，謝謝!
-
Source
Rabbit
-
Applications
WB,ELISA
-
Reactivity
Human,Mouse
-
Dilution
WB 1:500-2000 ELISA 1:5000-20000
-
Storage
-20°C/1 year
-
Specificity
ATX7 Polyclonal Antibody detects endogenous levels of protein.
-
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-
Immunogen
Synthesized peptide derived from human protein . at AA range: 260-340
-
Uniprot No
O15265
-
Form
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
-
Clonality
Polyclonal
-
Isotype
IgG
-
Background
ataxin 7(ATXN7) 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 transmi
-
Other
ATXN7 SCA7, Ataxin-7 (Spinocerebellar ataxia type 7 protein)
-
Concentration
1 mg/ml
| Product | Reactivity | Applications | Conjugation | Catalog | Images |
|---|
采購中心
化工儀器網