ALG9 Polyclonal Antibody

• Background :

  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.

• Description :

  This is a ALG9 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms :

  ALG9, ALG9, Alpha-1,2-mannosyltransferase ALG9, Asparagine-linked glycosylation protein 9 homolog, Disrupted in bipolar disorder protein 1

• Swiss Prot :

  Q9H6U8

• Accession Number :

  BC009255

• Reactivity :

  Human, Mouse

• Immunogen :

  Recombinant protein of human ALG9

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Polyclonal Antibody

• Applications :

  IHC, ELISA

• Purification Method :

  Affinity purification

• Assay Type :

  Antibody

• Concentration :

  0.3 mg/mL

• Dilution :

  IHC 1:50-1:200

• Buffer :

  PBS with 0.05% sodium azide and 50% glycerol, PH7.4

• Storage Conditions :

  Store at -20°C. Avoid freeze / thaw cycles.

• Host or Source :

  Rabbit

• Isotype :

  IgG