Background：The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome （WWS） and limb-girdle muscular dystrophy type 2K （LGMD2K）. Several transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：Dolichyl phosphate mannose protein mannosyltransferase 1,Dolichyl phosphate mannose protein mannosyltransferase1,Dolichyl-phosphate-mannose--protein mannosyltransferase 1,LGMD2K,MDDGA1,MDDGB1,MDDGC1,POMT 1,POMT1,POMT1,Protein O mannosyl transferase 1,Protein O mannosyl transferase1,Protein O-mannosyl-transferase 1,Rotate abdomen,Drosophila,homolog of,RT
Host：Rabbit
Reactivity：Human
Applications：IHC,ELISA
Concentration：0.4mg/mL
Immunogen：Synthetic peptide of human POMT1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
Dilution：IHC 1：50-1：200
Swissprot：Q9Y6A1
Isotype：IgG
Research Areas：Cancer, Neuroscience, Signal transduction
