Browse our AFG3L2 (AFG3L2) ELISA Kits

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AFG3 ATPase Family Gene 3-Like 2 (S. Cerevisiae) ELISA Kits (AFG3L2)
On are 0 AFG3 ATPase Family Gene 3-Like 2 (S. Cerevisiae) (AFG3L2) ELISA Kits from different suppliers available. Additionally we are shipping AFG3L2 Antibodies (63) and AFG3L2 Proteins (3) and many more products for this protein. A total of 70 AFG3L2 products are currently listed.
2310036I02Rik, AW260507, Emv66, MGC147390, par, SCA28, si:ch211-12e1.4, SPAX5
list all ELISA KIts Gene Name GeneID UniProt
Human AFG3L2 AFG3L2 10939 Q9Y4W6
Rat AFG3L2 AFG3L2 307350  
Mouse AFG3L2 AFG3L2 69597 Q8JZQ2

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More ELISA Kits for AFG3L2 Interaction Partners

Human AFG3 ATPase Family Gene 3-Like 2 (S. Cerevisiae) (AFG3L2) interaction partners

  1. Deletion of AFG3L2 associated with spinocerebellar ataxia type 28 in the context of multiple genomic anomalies.

  2. AOA2 (show SETX ELISA Kits) with myoclonus associated with mutations in SETX (show SETX ELISA Kits) and AFG3L2

  3. This study that AFG3L2 mutations are another important cause, albeit rare, of a late-onset ataxic PEO (show POLG ELISA Kits) phenotype due to a disturbance of mtDNA maintenance.

  4. StAR proteolysis is executed by at least 2 mitochondrial proteases, the matrix LON (show LONP1 ELISA Kits) protease and the inner membrane complexes of the metalloproteases AFG3L2 and AFG3L2:SPG7/paraplegin (show SPG7 ELISA Kits).

  5. Here, we report on a novel AFG3L2 mutation in a patient with slowly progressive ataxia and a positive family history.

  6. Identification of a partial AFG3L2 deletion and subsequent functional studies reveal loss of function as the most likely disease mechanism.

  7. Both full-length and truncated COX1 (show COX1 ELISA Kits) proteins physically interact with AFG3L2.

  8. These findings expand the phenotype associated with AFG3L2 mutations and suggest that AFG3L2-related disease should be considered in the differential diagnosis of spastic ataxias.

  9. The mutations of SCA28 are associated with amino acid changes in evolutionarily conserved residues of the alleged SCA28 gene, and indicate SCA28 as the sixth recognized SCA genotype caused by point mutations.

  10. We further confirm both the involvement of AFG3L2 gene in Spinocerebellar ataxia type 28 (SCA28) and the presence of a mutational hotspot in exons 15-16.

Mouse (Murine) AFG3 ATPase Family Gene 3-Like 2 (S. Cerevisiae) (AFG3L2) interaction partners

  1. total ablation of the m-AAA (show AAAS ELISA Kits) protease, by deleting both Afg3l2 and its paralogue Afg3l1 (show AFG3L1 ELISA Kits), triggers progressive motor dysfunction and demyelination, owing to rapid oligodendrocyte cell death

  2. AFG3L2 is critical to the surveillance mechanism that acts as a sensor to couple the synthesis of mitochondrial proteins with organelle fitness, thus ensuring coordinated assembly of the oxidative phosphorylation complexes from two sets of ribosomes.

  3. defective mitochondrial protein (show COX6B2 ELISA Kits) synthesis, leading to early-onset fragmentation of the mitochondrial network, is a central causative factor in AFG3L2-related neurodegeneration.

  4. These findings shed new light in the molecular mechanisms underlining neurodegeneration caused by AFG3L2 mutations.

  5. Data show that Afg3l1 or Afg3l2 are required for maturation of newly imported paraplegin subunits after their cleavage by MPP.

  6. AFG3L2 mutant mouse models display a marked impairment of axonal development with delayed myelination and poor axonal growth.

  7. Spg7 (show SPG7 ELISA Kits) and Afg3l2 double mutants show an early-onset ataxic phenotype, indicating a role of the m-AAA (show AAAS ELISA Kits) proteases in cerebellar degeneration.

  8. demonstrate that cerebellum is the neuronal tissue with the highest susceptibility to reduced Afg3l2 dosage; propose that the Afg3l2 heterozygous mouse is an excellent model to unravel the pathological cascade leading to spinocerebellar ataxia type 28

AFG3L2 Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with AFG3L2

  • AFG3 ATPase family gene 3-like 2 (S. cerevisiae) (AFG3L2) Elisa Kit
  • AFG3 ATPase family gene 3-like 2 (S. cerevisiae) (afg3l2) Elisa Kit
  • AFG3 ATPase family member 3-like 2 (S. cerevisiae) (afg3l2) Elisa Kit
  • AFG3 ATPase family member 3-like 2 (S. cerevisiae) (AFG3L2) Elisa Kit
  • AFG3 ATPase family member 3-like 2 (S. cerevisiae) (Afg3l2) Elisa Kit
  • AFG3(ATPase family gene 3)-like 2 (yeast) (Afg3l2) Elisa Kit
  • 2310036I02Rik Elisa Kit
  • AW260507 Elisa Kit
  • Emv66 Elisa Kit
  • MGC147390 Elisa Kit
  • par Elisa Kit
  • SCA28 Elisa Kit
  • si:ch211-12e1.4 Elisa Kit
  • SPAX5 Elisa Kit

Protein level used designations for AFG3L2

AFG3 ATPase family gene 3-like 2 (S. cerevisiae) , AFG3 ATPase family gene 3-like 2 , AFG3 ATPase family gene 3-like 2-like , AFG3-like protein 2-like , AFG3-like protein 2 , AFG3-like protein 2 (Paraplegin-like protein) , ATPase family gene 3, yeast , paraplegin-like protein

455507 Pan troglodytes
578526 Strongylocentrotus purpuratus
703079 Macaca mulatta
780216 Xenopus (Silurana) tropicalis
100018022 Monodelphis domestica
100367333 Saccoglossus kowalevskii
100410379 Callithrix jacchus
100448741 Pongo abelii
100484304 Ailuropoda melanoleuca
569168 Danio rerio
421036 Gallus gallus
490560 Canis lupus familiaris
515757 Bos taurus
443667 Xenopus laevis
10939 Homo sapiens
307350 Rattus norvegicus
69597 Mus musculus
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