SLC25A45 (solute carrier family 25 member 45) is a 288 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, SLC25A45 contains three Solcar repeats and localizes to the mitochondrion inner membrane. Due to alternative splicing events, four known isoforms exist for SLC25A45. The human gene encoding SLC25A45 localizes to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene located on chromosome 11. Other disorders associated with defects in chromosome 11 include Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFIHCELISA
recommended for detection of SLC25A45 of human origin by WB, IP, IF, IHC(P) and ELISA: