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ATXN7 antibody - middle region

Catalog Number:OM106293
OM106293
Discount Price
OM106293-100ul
1~2 Week
100ul
OM106293-50ul
50ul
OM106293-20ul
20ul
1~2 Week
Product Profile
Product Name ATXN7 antibody - middle region
Antibody Type Primary Antibodies
Immunogen The immunogen for anti-ATXN7 antibody: synthetic peptide directed towards the middle region of human ATXN7
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
Species Reactivity Bovine,Dog,Guinea Pig,Horse,Human,Mouse,Pig,Rabbit,Rat
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol ATXN7
Gene Synonyms ADCAII
OPCA3
SCA7
Gene Full Name Ataxin 7
Gene Summary ATXN7 is involved in neurodegeneration. ATXN7 acts as component of the STAGA transcription coactivator-HAT complex. ATXN7 mediates the interaction of STAGA complex with the CRX and is involved in CRX-dependent gene activation.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. This locus has been mapped to chromosome 3, and it has been determined that the diseased allele associated with Spinocerebellar ataxia-7, contains 38-130 CAG repeats (near the N-terminus), compared to 7-17 in the normal allele. The exact function of this gene is not known, however, since the encoded protein contains a nuclear localization sequence, and is found to be localized in the nucleus, it has been postulated to be a potential transcription factor. Alternative splicing, resulting in transcript variants encoding different isoforms, has been noted for this gene.
Alternative Names ADCAII
OPCA3
SCA7
Molecular Weight(MW) 95kDa
Sequence 892 amino acids
Database Links
Entrez Gene 6314
SwissProt ID O15265
Protein Accession NP_000324
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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