epitope corresponding to amino acids 839-961 mapping within an internal region of Sucrase-Isomaltase of human origin
Modification Notes
Sucrase-Isomaltase (SI) is a type II brush border membrane protein that plays an important role in the final stage of carbohydrate digestion. Sucrase-Isomaltase is a disaccharidase that catalyzes the hydrolysis of dietary sucrose and maltose and other products of starch digestion. The high degree of amino acid homology between isomaltase and sucrose indicate that the Sucrase-Isomaltase protein was evolved by partial gene duplication. The Sucrase-Isomaltase precursor is proteolytically cleaved when exposed to pancreatic proteases in the intestinal lumen and localizes to the apical membrane of adult intestinal enterocytes along the intestinal crypt-villus axis. Sucrase-Isomaltase protein deficiency results in osmotic diarrhea due to an inability to hydrolyze intestinal disaccharides into component monosaccharides. Congenital Sucrase-Isomaltase deficiency (CSID) is an autosomal recessive human disorder characterized by reduced activities of Sucrase-Isomaltase
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of Sucrase-Isomaltase of human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 839-961 mapping within an internal region of Sucrase-Isomaltase of human origin
Tissue Specificity
epitope corresponding to amino acids 839-961 mapping within an internal region of Sucrase-Isomaltase of human origin
Application Notes
recommended for detection of Sucrase-Isomaltase of human origin by WB, IP, IF and ELISA:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.