SLC25A46 (solute carrier family 25 member 46) is a 418 amino acid multi-pass membrane protein that belongs to the the SLC25 family of mitochondrial carriers that are responsible for transporting metabolites across the inner mitochondrial membrane. Expressed in a variety of tissues, SLC25A46 contains two Solcar repeats and localizes to the mitochondrion inner membrane. The human gene encoding SLC25A46 localizes to chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
recommended for detection of SLC25A46 of mouse, rat, human, and zebra fish origin by WB, IP and ELISA: