recommended for detection of MFT of mouse, rat and human origin by WB, IP and ELISA; also reactive with additional species, including canine
Modification Notes
Folate is an essential vitamin that must be obtained from food intake through intestinal absorption in mammals. Folate and reduced folic acid derivatives bind to the folate receptor (FR) family, which mediates the endocytosis of 5-methyltetrahydofolate into the cell. MFT (Mitochondrial folate transporter/carrier), also known as Solute carrier family 25 member 32 (SLC25A32), is a 315 amino acid multi-pass membrane protein that regulates the influx of folate into the mitochondria. MFT also functions to complement glycine auxotrophy. Mutations in the gene encoding MFT may be involoved in certain cases of multiple acyl-CoA dehydrogenase deficiency (MADD), in which there is no mutation in EFTA or EFTB genes. MADD is a autosomal recessively inherited disorder in which fatty acid, amino acid and choline metabolism is disrupted, leading to a clinical manisfestation of hypoglycemia, hypotonia, hepatomegaly, metabolic acidosis and dysplastic kidneys.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of MFT of mouse rat and human origin by WB IP and ELISA also reactive with additional species including canine
Tissue Specificity
recommended for detection of MFT of mouse, rat and human origin by WB, IP and ELISA; also reactive with additional species, including canine