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Abnova/ATXN1 monoclonal antibody, clone 2F5/1kit/MAB10450
  • Abnova/ATXN1 monoclonal antibody, clone 2F5/1kit/MAB10450

Abnova/ATXN1 monoclonal antibody, clone 2F5/1kit/MAB10450

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貨號: MAB10450
品牌: Abnova
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  • 常見問題
      • Specification
      • Gene Info
      • Disease
      • Related Products
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      • Specification
      • Product Description:
      • 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:
      • PDF DownloadDownload
      • Applications
      • Western Blot (Transfected lysate)
      • 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.
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • 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
      • 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 Cytometry
      • Flow cytometric analysis of Jurkat cells using ATXN1 monoclonal antibody, clone 2F5 (Cat # MAB10450) (green) and negative control (purple).
      • Application Image
      • Western Blot (Transfected lysate)
      • Western Blot (Transfected lysate)
      • enlarge
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • enlarge
      • Immunofluorescence
      • Immunofluorescence
      • enlarge
      • Enzyme-linked Immunoabsorbent Assay
      • Flow Cytometry
      • Flow Cytometry
      • enlarge
      • Gene Information
      • Entrez GeneID:
      • 6310
      • Gene Name:
      • ATXN1
      • Gene Alias:
      • ATX1,D6S504E,SCA1
      • Gene Description:
      • ataxin 1
      • Omim ID:
      • 164400, 601556
      • Gene Ontology:
      • Hyperlink
      • Gene Summary:
      • 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
      • Other Designations:
      • OTTHUMP00000016065,OTTHUMP00000039306,olivopontocerebellar ataxia 1, autosomal dominant,spinocerebellar ataxia 1 (olivopontocerebellar ataxia 1, autosomal dominant, ataxin 1)
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      • Cerebellar Ataxia
      • Chronic Disease
      • Cognition
      • Dementia, Vascular
      • Diseases in Twins
      • Epilepsy
      • Fragile X Syndrome
      • Fragile X syndrome
      • Friedreich Ataxia
      • Friedreich"s ataxia
      • Genetic Predisposition to Disease
      • Genomic Instability
      • Huntington Disease
      • Huntington disease
      • Machado-Joseph Disease
      • Muscular Atrophy, Spinal
      • Myoclonic Epilepsies, Progressive
          • ... see more
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