OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
This Recombinant OPA1 protein is produced in HEK-293 Cells.
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Catalog No. ABIN2727921
$1,112.40
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20 μg
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United States
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Quick Overview for OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag) (ABIN2727921)
Target
See all OPA1 Proteins
OPA1
(Optic Atrophy 1 (Autosomal Dominant) (OPA1))
Protein Type
Recombinant
Origin
Human
Source
HEK-293 Cells
Application
Antibody Production (AbP), Standard (STD)
Purity
> 80 % as determined by SDS-PAGE and Coomassie blue staining
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Protein Characteristics
- Transcript Variant 3
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Purification tag / Conjugate
- This OPA1 protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human Optic atrophy 1 (autosomal dominant) (OPA1), nuclear gene encoding mitochondrial protein, transcript variant 3 (transcript variant 3) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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Optic Atrophy 1 (Autosomal Dominant) (OPA1) (AA 851-960) protein (GST tag)
OPA1 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AP, AA
Optic Atrophy 1 (Autosomal Dominant) (OPA1) (AA 1-960) protein (GST tag)OPA1 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AP, AA
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Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
Comment
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The tag is located at the C-terminal.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
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Background
- This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. 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. Multiple transcript variants encoding different isoforms have been found for this gene.
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Molecular Weight
- 109.2 kDa
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NCBI Accession
- NP_570845
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Pathways
- Tube Formation
Target
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