Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) Proteins (OPA3)

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Additionally we are shipping OPA3 Antibodies (25) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
OPA3 403187 Q505D7
OPA3 80207 Q9H6K4
OPA3 308409  
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Top OPA3 Proteins at antibodies-online.com

Showing 9 out of 10 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 30 to 35 Days
$4,331.68
Details
Insect Cells Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 50 Days
$5,442.50
Details
Yeast Zebrafish His tag   1 mg Log in to see 60 to 71 Days
$2,352.17
Details
Yeast Cow His tag   1 mg Log in to see 60 to 71 Days
$2,458.50
Details
HOST_HEK-293 Cells Human Myc-DYKDDDDK Tag Validation with Western Blot 20 μg Log in to see 10 to 12 Days
$785.40
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 11 to 12 Days
$405.71
Details
HOST_Escherichia coli (E. coli) Human T7 tag,His tag   100 μg Log in to see 15 to 18 Days
$678.00
Details
HOST_Escherichia coli (E. coli) Mouse T7 tag,His tag   100 μg Log in to see 15 to 18 Days
$726.00
Details
HOST_Escherichia coli (E. coli) Rat T7 tag,His tag   100 μg Log in to see 15 to 18 Days
$742.00
Details

OPA3 Proteins by Origin and Source

Origin Expressed in Conjugate
Mouse (Murine) ,
,
Human , ,
, , ,
Rat (Rattus)

More Proteins for Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3) Interaction Partners

Human Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3) interaction partners

  1. Mutations of the OPA3 gene can cause either autosomal dominant or autosomal recessive optic atrophy.

  2. Report the results of a comprehensive study on OPA3 mutations, including the mutation spectrum and its prevalence in a large cohort of ADOA patients, the associated clinical phenotype and the functional characterisation of a newly identified OPA3 mutant.

  3. A novel missense mutation identifies OPA3 as the cause of a complex neurological disorder with marked lower limb dystonia.

  4. OPA1 (show OPA1 Proteins) mutations are the most common genetic defects identified in patients with suspected Autosomal-dominant optic atrophy (DOA), whereas OPA3 mutations are very rare in isolated optic atrophy cases.

  5. OPA3, as an integral mitochondrial outer membane perotein, has a crucial role in mitochondrial fission, and provides a direct link between mitochondrial morphology and optic atrophy.

  6. two missense mutations in OPA3 in two families affected by autosomal dominant optic atrophy and cataract (ADOAC)

  7. OPA1 (show OPA1 Proteins) mutations, mtDNA mutations, and OPA3 mutations in 980 patients Leber's hereditary optic neuropathy and autosomal dominant optic atrophy

  8. The mouse ortholog of OPA3 purifies with mitochondrial inner membranes.

  9. The mouse ortholog of OPA3 purifies with mitochondria

  10. type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews

Zebrafish Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3) interaction partners

  1. mitochondrial OPA3 is required to limit HMG-CoA-derived MGC and protect the electron transport chain against inhibitory compounds in a zebrafish model of Costeff Syndrome

Cow (Bovine) Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3) interaction partners

  1. The present study is the first report of the OPA3 mutation in dilated cardiomyopathy affected cows outside Switzerland.

  2. the nonsense mutation c.343C>T in the bovine OPA3 gene causes the late-onset dilated cardiomyopathy in Red Holstein cattle.

OPA3 Protein Profile

Protein Summary

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with OPA3

  • optic atrophy 3 (opa3)
  • optic atrophy 3 (Opa3)
  • optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) (OPA3)
  • D630048P19Rik protein
  • Gm472 protein
  • Gm1425 protein
  • MGA3 protein

Protein level used designations for OPA3

optic atrophy 3 protein homolog , mitochondrial optic atrophy 3 protein , Optic atrophy 3 (Iraqi-Jewish 'optic atrophy plus') , optic atrophy 3 protein , optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)

GENE ID SPECIES
497278 Danio rerio
403187 Mus musculus
523579 Bos taurus
80207 Homo sapiens
308409 Rattus norvegicus
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