ATXN3 Polyclonal Antibody | G-AB-00206
Gentaur Antibodies
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Gentaur Antibodies
ATXN3 Polyclonal Antibody | G-AB-00206
- SKU:
- G-AB-00206
- Availability:
- 3 to 5 Working Days
- Host:
- Rabbit
- Reactivity:
- Human
ATXN3 Polyclonal Antibody | G-AB-00206 | Gentaur Antibodies
Overview: Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by this gene contains (CAG) n repeats in the coding region, and the expansion of these repeats from the normal 12-44 to 52-86 is one cause of Machado-Joseph disease. There is a negative correlation between the age of onset and CAG repeat numbers. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
Category Type: Polyclonal Antibody
Research Areas: Cancer, Epigenetics and Nuclear Signaling, Neuroscience
Synonyms: AT3, Ataxin 3, ataxin 3 variant h, ataxin 3 variant m, ataxin 3 variant ref, Ataxin-3, ATX3, EC 3.4.22, JOS, Machado Joseph disease, MJD, Olivopontocerebellar ataxia 3, OTTHUMP00000221583, Rsca3, Spinocerebellar ataxia type 3 protein
Reactivity: Human
Host: Rabbit
Isotype: IgG
Gene ID:
Accession #:
Clonality: Polyclonal
Immunogen: Recombinant Human Ataxin-3 protien
Clone #:
Conjugation: Unconjugated
Swissprot: P54252
Santa Cruz:
Calculated MW: 41 kDa
Observed MW: 41 kDa, 22 kDa
Concentration: 2 mg/mL
Buffer: PBS with 0.05% Proclin300 and 50% glycerol, pH7.4.
Purification method: Affinity purification
Application: WB, IHC
Dilution: WB 1:500-1:2000 IHC 1:50-1:200
Storage: Store at -20°C. Avoid freeze / thaw cycles.
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