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:

  0.1 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