FLCN Polyclonal Antibody

• Background:

  This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms.

• Description:

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

• Synonyms:

  FLCN, BHD, FLCL

• Gene ID:

  201163

• Swiss Prot:

  Q8NFG4

• Reactivity:

  Human, Mouse, Rat

• Immunogen:

  Recombinant fusion protein of human FLCN (NP_653207.1) .

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  IF

• Purification Method:

  Affinity purification

• Assay Type:

  Antibody

• Concentration:

  1 mg/mL

• Dilution:

  IF 1:50-1:200

• Buffer:

  PBS with 0.02% sodium azide, 50% glycerol, pH7.3

• Storage Conditions:

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

• Host or Source:

  Rabbit

• Isotype:

  IgG