AFG3L2 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.

• NCBI Gene ID:

  10939

• Swiss Prot:

  Q9Y4W6

• Host:

  Rabbit

• Reactivity:

  Human, Mouse, Rat

• Immunogen:

  Recombinant fusion protein containing a sequence corresponding to amino acids 538-797 of human AFG3L2 (NP_006787.2) .

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Primary Antibodies

• Field of Research:

  Cancer, Cell Cycle, Neuroscience, Signal Transduction

• Purification:

  Affinity purification

• Positive Control:

  LO2

• Concentration:

  Batch dependent

• Buffer:

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

• Modification:

  None

• Shipping Conditions:

  Blue Ice

• Storage Conditions:

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

• Calculated Molecular Weight:

  Observed: 89kDa

• Fragment:

  IgG

• Symbol:

  AFG3L2

• Positive Control 2:

  293T

• Positive Control 3:

  HeLa

• Positive Control 4:

  Mouse brain

• Positive Control 5:

  Mouse heart

• Positive Control 6:

  Mouse kidney

• NCBI Official Name:

  AFG3-like AAA ATPase 2

• NCBI Organism:

  Homo sapiens

• Other Product Names:

  AFG3L2, FLJ25993, SCA28, SPAX5

• Tested Applications:

  WB, IHC, IF

• Physical Properties:

  Liquid