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For research use only.

Verified Samples Verified Samples in WB: 293T, Human fetal brain
Verified Samples in IHC: Human thyroid cancer, Human liver cancer
Dilution WB 1:500-1:2000,  IHC 1:50-1:200
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen Recombinant protein of human ATXN1
Synonyms ATX1,  Ataxin-1,  Atxn1,  D6S504E,  OTTHUMP00000016065,  SCA1,  Spinocerebellar ataxia type 1 protein,  alternative ataxin1
Swissprot
Calculated MW 87 kDa
Cellular Localization Cytoplasm. Nucleus. Colocalizes with USP7 in the nucleus.
Concentration 0.3 mg/mL
Buffer PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method Affinity purification
Research Areas Epigenetics and Nuclear Signaling,  Neuroscience
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background 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.
Other Clones

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Unconjugated

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