AFG3L2 Polyclonal Antibody

• Background:

  This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

• Description:

  This is a AFG3L2 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms:

  AFG3L2, SCA28, SPAX5

• Gene ID:

  10939

• Swiss Prot:

  Q9Y4W6

• Reactivity:

  Human, Mouse, Rat

• Immunogen:

  Recombinant fusion protein of human AFG3L2 (NP_006787.2) .

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  WB, IHC

• Purification Method:

  Affinity purification

• Assay Type:

  Antibody

• Concentration:

  1 mg/mL

• Dilution:

  WB 1:200-1:2000 IHC 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.

• Calculated Molecular Weight:

  88 kDa

• Observed Molecular Weight:

  89 kDa

• Host or Source:

  Rabbit

• Isotype:

  IgG