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Ataxin 3 Rabbit Polyclonal Antibody

CAT: 0013-GTR17705724-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17705724-01Size:50 μL
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Description
Ataxin 3 Rabbit Polyclonal Antibody
Product Name Alternative
AT3; ATX3; JOS; MJD; MJD1; SCA3; 2210008M02Rik; ataxin-3; Rsca3; ATX3_HUMAN; ATXN3; Machado-Joseph disease protein 1; Spinocerebellar ataxia type 3 protein; 3.4.19.12; ATX3_MOUSE; Machado-Joseph disease protein 1 homolog; ATX3_RAT; ataxin 3; Machado-Joseph disease (spinocerebellar ataxia 3, olivopontocerebellar ataxia 3, autosomal dominant, ataxin 3)
UniProt
P54252
Reactivity
Human, Mouse, Rat
Immunogen
KLH conjugated synthetic peptide derived from human Ataxin 3 (51-150/364aa)
Target
ATXN3
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Epigenetics and Nuclear Signaling, Neurodegenerative Disease, Neuroscience, Ubiquitylation
Purification
Affinity purified by Protein A
Concentration
1mg/ml
Dilution
IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500
Form
Liquid
Molecular Weight
42 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Prediction Reactivity
Bovine, Canine, Equine, Porcine, Sheep
Tested Applications
IF, IHC-Fr, IHC-P
Host or Source
Rabbit
Preservative
0.01M TBS (pH7.4) with 1% rAlbumin, 0.02% Proclin300 and 50% Glycerol.
Isotype
IgG

UniProtKB · P54252

Ataxin-3

ATX3_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P54252
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATXN3
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.4.19.12
Processing
—
Secondary accessions
A7LFZ5, D6RDL9, E9PB63, O15284, O15285, O15286, Q8N189, Q96TC3, Q96TC4, Q9H3N0
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicingTriplet repeat expansion

Molecular function

HydrolaseProteaseThiol protease

PTM

Isopeptide bondPhosphoproteinUbl conjugation

Cellular component

LysosomeMembraneNucleus

Disease

NeurodegenerationSpinocerebellar ataxia

Domain

Repeat

Biological process

TranscriptionTranscription regulationUbl conjugation pathway

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