Skip to main content

Sulfatase Modifying Factor 1/SUMF1 Products

Mammalian sulfatases have a common CXPXR motif, in which the Cys residue is post-translationally modified to a Calpha-formylglycine (FGly) residue. This modification is essential for catalytic activity of all sulfatases and is catalyzed by FGly generating enzyme (FGE) encoded by sulfatase modifying factor 1 (SUMF1). FGE deficiency causes multiple sulfatase deficiency (MSD), a rare autosomal recessive disorder. SUMF2 does not have FGly enzymatic activity, but may compete with SUMF1 for the same substrate.

Show More

11 results for "Sulfatase Modifying Factor 1/SUMF1" in Products

11 results for "Sulfatase Modifying Factor 1/SUMF1" in Products

Sulfatase Modifying Factor 1/SUMF1 Products

Mammalian sulfatases have a common CXPXR motif, in which the Cys residue is post-translationally modified to a Calpha-formylglycine (FGly) residue. This modification is essential for catalytic activity of all sulfatases and is catalyzed by FGly generating enzyme (FGE) encoded by sulfatase modifying factor 1 (SUMF1). FGE deficiency causes multiple sulfatase deficiency (MSD), a rare autosomal recessive disorder. SUMF2 does not have FGly enzymatic activity, but may compete with SUMF1 for the same substrate.

Show More
Applications: WB, ELISA
Reactivity: Human, Mouse
Catalog #: NBP3-40140
Applications: ELISA
Applications: IHC
Reactivity: Human
Applications: WB
Applications: PAGE
Catalog #: NBP3-40139
Applications: ELISA
Applications: PAGE
Applications: AC
Applications: WB, IP
Reactivity: Human, Mouse
Applications: WB
Reactivity: Mouse
Applications: WB
Reactivity: Human
Results Per Page
5 10 25 50
/ 1