MAFB Polyclonal Antibody, 100ul Pipette Micro Tips Mutations in SLC22A5 (solute carrier

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

The encoded protein catalyzes transfer of UDP-xylose to serine residues of an acceptor protein substrate

These filaments| along with actin microfilaments and microtubules| compose the cytoskeleton of epithelial cells

but upstream of CASP3/caspase-3 as well as CCND1/cyclin D1 and E2F1

MAFB Polyclonal Antibody, 100ul Pipette Micro Tips Mutations in SLC22A5 (solute carrierThe protein encoded by this gene is a basic leucine zipper (bZIP) transcription factor that plays an important role in the regulation of lineage specific hematopoiesis. The encoded nuclear protein represses ETS1 mediated transcription of erythroid specific genes in myeloid cells. This gene contains no introns.