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anti-Rat (Rattus) SLC25A32 Antibodies:
anti-Human SLC25A32 Antibodies:
anti-Mouse (Murine) SLC25A32 Antibodies:
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Human Polyclonal SLC25A32 Primary Antibody for WB - ABIN4892382
Titus, Moran: Retrovirally mediated complementation of the glyB phenotype. Cloning of a human gene encoding the carrier for entry of folates into mitochondria. in The Journal of biological chemistry 2001
These data demonstrate that the loss of functional Slc25a32 results in cranial neural tube defects (NTDs) in mice and has also been observed in a human NTD patient.
A novel SLC25A32 homozygous variant is associated with severe neuromuscular phenotype.
SLC25A32 gene polymorphism could be a risk factor for lower folate concentration and future fracture.
Compares and contrasts all the known human SLC25A (show SLC25A25 Antibodies)* genes and includes functional information.
identified residues in the walls and at the base of the transport cavity that are involved in substrate recognition by the MFT
Patient with SLC25A32 deficiency was able to have a successful pregnancy after fertilization in vitro.
This gene encodes a member of the P(I/L)W subfamily of mitochondrial carrier family transport proteins. The encoded protein transports folate across the inner mitochondrial membrane. Alternatively spliced transcript variants have been described.
mitochondrial folate transporter/carrier
, solute carrier family 25, member 32
, solute carrier family 25 (mitochondrial folate carrier) , member 32