Mouse monoclonal antibody raised against recombinant ATXN1.
Immunogen:
Recombinant protein corresponding to human ATXN1.
Host:
Mouse
Theoretical MW (kDa):
87
Reactivity:
Human
Form:
Liquid
Isotype:
IgG1
Recommend Usage:
Western Blot (1:500-1:2000)Immunohistochemistry (1:200-1:1000)Immunofluorescence (1:200-1:1000)Flow Cytometry (1:200-1:400)ELISA (1:10000)The optimal working dilution should be determined by the end user.
Storage Buffer:
In ascitic (0.03% sodium azide)
Storage Instruction:
Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Note:
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Datasheet:
Download
Applications
Western Blot (Transfected lysate)
Western blot analysis using ATXN1 monoclonal antibody, clone 2F5 (Cat # MAB10450) against HEK293 (1) and ATXN1-hIgGFc transfected HEK293 (2) cell lysate.
Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue (A) and lung cancer tissue (B) using ATXN1 monoclonal antibody, clone 2F5 (Cat # MAB10450) with DAB staining.
Immunofluorescence
Immunofluorescence analysis of NTERA-2 cells using ATXN1 monoclonal antibody, clone 2F5 (Cat # MAB10450) (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
Enzyme-linked Immunoabsorbent Assay
Flow Cytometry
Flow cytometric analysis of Jurkat cells using ATXN1 monoclonal antibody, clone 2F5 (Cat # MAB10450) (green) and negative control (purple).
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 41-81 CAG repeats, compared to 6-39 in the normal allele. At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq
购物车为空，快去购物吧！
4000-520-616
咨询顾问
特别 提示
Download
