CD55 Polyclonal Antibody, 100ul[BT-AP02456] Cell Screening and Imaging Mutations in this gene may

Mutations in this gene may result in Netherton syndrome

and the C-terminal segment of this domain is characterized by ten conserved cysteine residues

SLC30A4 (solute carrier family 30 member 4)

Compatible with VT1

Intracellular or ectopic expression of this protein expands hematopoietic stem and progenitor cells in vivo and in vitro

CD55 Polyclonal Antibody, 100ul[BT-AP02456] Cell Screening and Imaging Mutations in this gene mayCytochrome b5 type A encoded by CYB5A is a membrane bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl CoA desaturase activity. Defects in CYB5A are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for CYB5A.