Anti-Human/Mouse ALG9 Polyclonal Antibody

This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12983
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ALG9
Specificity Ubiquitously expressed; with highest levels in heart, liver and pancreas.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q9H6U8
Concentration 0.1 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names ALG9,ALG9,Alpha-1,2-mannosyltransferase ALG9,Asparagine-linked glycosylation protein 9 homolog,Disrupted in bipolar disorder protein 1
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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