SLC35F5 (Solute carrier family 35 member F5), also known as Hepatitis C virus NS5A-transactivated protein 3, is a 523 amino acid multi-pass membrane protein that belongs to the SLC35F solute transporter family. Existing as two alternatively spliced isoforms, SLC35F5 functions as a putative solute transporter. The gene encoding SLC35F5 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the chromosome 2-localized ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes, which also map to chromosome 2.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of SLC35F5 of mouse rat and human origin by WB IP and ELISA
Tissue Specificity
recommended for detection of SLC35F5 of mouse, rat and human origin by WB, IP and ELISA