Thermo Fisher Scientific ATXN7L1 Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:1,000

-

Product Specifications

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Synthesized peptide derived from human ATXN7L1 isoform 2. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:ATXN7L1,uniProtId:Q9ULK2-1,ncbiNodeId:9606,antigenRange:105-129,antigenLength:861,antigenImageFileName:PA5-68101_ATXN7L1_Q9ULK2-1_Rabbit.svg,antigenImageFileNamePDP:PA5-68101_ATXN7L1_Q9ULK2-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Storage conditions

-20°C

Shipping conditions

Wet ice

RRID

AB_2691559

Target Information

ATXN7L1 (ataxin-7-like protein 1) is an 833 amino acid protein that contains one SCA7 domain. The ATXN7L1 gene is conserved in chimpanzee, canine, mouse, rat and chicken, and maps to human chromosome 7q22.3. Chromosome 7 is about 158 million bases long, encodes over 1,000 genes and makes up about 5%of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.