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ATXN7L2 Rabbit anti-Human, Polyclonal, Bioss
SDP

Rabbit Polyclonal Antibody

Supplier:  Bioss BS7976R

Encompass_Preferred

Catalog No. 50-198-8175


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Description

Description

SCA7 is an autosomal dominant neurodegenerative disorder characterized by ataxia and selective neuronal cell loss caused by the expansion of a translated CAG repeat encoding a polyglutamine tract in ataxin-7, which is the SCA7 gene product. Ataxin-7 is a nuclear protein that is expressed within neurons both affected and unaffected in SCA7 pathology with subcellular localization being variable depending upon the neuronal subtype. Polyglutamine expanded in ataxin-7 may carry out its pathogenic effects in the nucleus by altering the matrix-associated nuclear structure and/or by disrupting nucleolar function.ATXN7L2 (Ataxin-7-like protein 2) is a 722 amino acid protein that contains a SCA7 domain, which is highly conserved through all members of the ATXN7 gene family. The gene encoding ATXN7L2 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome.
Specifications

Specifications

ATXN7L2
Polyclonal
Unconjugated
ATXN7L2
2610528J18Rik; ataxin 7 like 2; ataxin 7-like 1; ataxin 7-like 2; Ataxin-7-like protein 2; ATXN7L2; mFLJ00381 protein; RGD1307047
Rabbit
Protein A
RUO
127002
-20°C
Liquid
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
1 μg/mL
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Q5T6C5
ATXN7L2
KLH conjugated synthetic peptide derived from human ATXN7L2.
100 μL
Primary
Human
Antibody
IgG
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