Thermo Fisher Scientific ATXN7L1 Monoclonal Antibody (OTI4B12), TrueMAB

Applications

Tested Dilution

Publications

Western Blot (WB)

1:2,000

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG1

Class

Monoclonal

Type

Antibody

Clone

OTI4B12

Immunogen

Full length human recombinant protein of human ATXN7L1 produced in HEK293T cell. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:ATXN7L1,uniProtId:Q9ULK2-1,ncbiNodeId:9606,antigenRange:1-861,antigenLength:861,antigenImageFileName:CF505710_ATXN7L1_Q9ULK2-1_House_mouse.svg,antigenImageFileNamePDP:CF505710_ATXN7L1_Q9ULK2-1_House_mouse_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

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

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Lyophilized

Concentration

1 mg/mL

Purification

Affinity chromatography

Storage buffer

PBS, pH 7.3, with 8% trehalose

Contains

no preservative

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, we recommend adding 100 µL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiments, we strongly recommend performing another round of desalting. (Zeba Spin Desalting Columns, 7KMWCO, 0.5 mL, Product # 89882)

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.