Product Synonym Names
Optic atrophy protein 1
Product Gene Name
anti-OPA1 antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O60313
Species Reactivity
Human, Mouse, Rat
Purity/Purification
Immunogen affinity purified
Immunogen
Amino acids 647-780 mapping within an internal region of OPA1 of human origin.
Storage Buffer
1*TBS (pH7.4), 1% BSA, 40% Glycerol.
Preservative
0.05% Sodium Azide.
Preparation and Storage
Aliquot and store at-20 degree C. Avoid repeated freeze/thaw cycles.
Other Notes
Small volumes of anti-OPA1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-OPA1 antibody
Western Blot (WB), Immunoprecipitation (IP), Immunofluorescence (IF)
NCBI/Uniprot data below describe general gene information for OPA1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_056375.2
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NCBI GenBank Nucleotide #
NM_015560.2
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UniProt Primary Accession #
O60313
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UniProt Secondary Accession #
D3DNW4; E5KLJ5; E5KLJ6; E5KLJ7; E5KLK1; E5KLK2[Other Products]
UniProt Related Accession #
O60313[Other Products]
Molecular Weight
107,568 Da
NCBI Official Full Name
dynamin-like 120 kDa protein, mitochondrial isoform 1 preproprotein
NCBI Official Synonym Full Names
OPA1, mitochondrial dynamin like GTPase
NCBI Official Symbol
OPA1 [Similar Products]
NCBI Official Synonym Symbols
NPG; NTG; MGM1; BERHS; largeG; MTDPS14
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NCBI Protein Information
dynamin-like 120 kDa protein, mitochondrial
UniProt Protein Name
Dynamin-like 120 kDa protein, mitochondrial
UniProt Synonym Protein Names
Optic atrophy protein 1
Protein Family
Dynamin-like 120 kDa protein
UniProt Gene Name
OPA1 [Similar Products]
UniProt Synonym Gene Names
KIAA0567 [Similar Products]
NCBI Summary for OPA1
The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]
UniProt Comments for OPA1
Dynamin-related GTPase that is essential for normal mitochondrial morphology by regulating the equilibrium between mitochondrial fusion and mitochondrial fission (PubMed:16778770, PubMed:17709429, PubMed:20185555, PubMed:24616225). Coexpression of isoform 1 with shorter alternative products is required for optimal activity in promoting mitochondrial fusion (PubMed:17709429). Binds lipid membranes enriched in negatively charged phospholipids, such as cardiolipin, and promotes membrane tubulation (PubMed:20185555). The intrinsic GTPase activity is low, and is strongly increased by interaction with lipid membranes (PubMed:20185555). Plays a role in remodeling cristae and the release of cytochrome c during apoptosis (). Proteolytic processing in response to intrinsic apoptotic signals may lead to disassembly of OPA1 oligomers and release of the caspase activator cytochrome C (CYCS) into the mitochondrial intermembrane space (). Plays a role in mitochondrial genome maintenance (PubMed:20974897, PubMed:18158317).
Research Articles on OPA1
1. Genetic testing identified disease-causing mutations in 34% of referred cases, with the majority of these in OPA1. Patients with mutations in OPA1 were more likely to have a family history of disease; however, 30.4% of patients without a family history were also found to have an OPA1 mutation.
Precautions
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