Anti-Human POMT1 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA10735
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human POMT1
Specificity Widely expressed. Highly expressed in testis, heart and pancreas. Detected at lower levels in kidney, skeletal muscle, brain, placenta, lung and liver.
Isotype IgG
Reacitivity Human
Clone
Uniprot Q9Y6A1
Concentration 0.4 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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