AFG3L2 rabbit pAb

• 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. [provided by RefSeq, Jul 2008]

• Description :

  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. [provided by RefSeq, Jul 2008],

• Product Name Alternative :

  AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)

• UniProt :

  Q9Y4W6

• Swiss Prot :

  Q9Y4W6

• Reactivity :

  Human; Rat; Mouse

• Immunogen :

  Synthesized peptide derived from human AFG3L2. at AA range: 744-793

• Target :

  AFG3L2

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000, ELISA 1:10000-20000

• Buffer :

  -20°C/1 year

• Molecular Weight :

  88kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  88kD

• Fragment :

  IgG

• Subcellular Location :

  Mitochondrion . Mitochondrion inner membrane ; Multi-pass membrane protein .

• Other Product Names :

  AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)

• Gene ID (Human) :

  10939