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ATXN1 Polyclonal Antibody

CAT: 0763-E-AB-10990-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0763-E-AB-10990-01Size:20 µL
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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.
Abbreviation
ATXN1
UniProt
P54253
Host
Rabbit
Reactivity
Human; Mouse; Rat
Immunogen
Recombinant protein of human ATXN1
Target
Alternative ataxin1; Ataxin-1; ATX1; ATX1; Atxn1; D6S504E; OTTHUMP00000016065; SCA1; Spinocerebellar ataxia type 1 protein
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
IHC
Field of Research
Epigenetics and Nuclear Signaling; Neuroscience
Purification
Affinity purification
Concentration
0.4 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Shipping Conditions
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Isotype
IgG

UniProtKB · P54253

Ataxin-1

ATX1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P54253
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATXN1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
Q17S02, Q9UJG2, Q9Y4J1
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicingTriplet repeat expansion

Cellular component

CytoplasmNucleus

Molecular function

DNA-bindingRepressorRNA-binding

PTM

Isopeptide bondPhosphoproteinUbl conjugation

Disease

NeurodegenerationSpinocerebellar ataxia

Biological process

TranscriptionTranscription regulation