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.

• Abbreviation:

  ALG9

• UniProt:

  Q9H6U8

• Host:

  Rabbit

• Reactivity:

  Human; Mouse

• Immunogen:

  Recombinant protein of human ALG9

• Target:

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

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Applications:

  IHC

• Purification:

  Affinity purification

• Concentration:

  0.1 mg/mL

• Dilution:

  IHC 1:50-1:200

• Buffer:

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

• Shipping Conditions:

  The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

• Storage Conditions:

  Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

• Isotype:

  IgG