OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes OPA1 Protéines
- OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant 3
- Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette OPA1 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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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
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product OPA1 Protéine
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- Indications d'application
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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 - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- 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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- Antigène
- OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
- Abstract
- OPA1 Produits
- Synonymes
- 1200011N24Rik Protein, AI225888 Protein, AI847218 Protein, lilr3 Protein, mKIAA0567 Protein, MGM1 Protein, NPG Protein, NTG Protein, largeG Protein, fk62d06 Protein, wu:fb77a10 Protein, wu:fk62d06 Protein, zgc:92092 Protein, OPA1, mitochondrial dynamin like GTPase Protein, optic atrophy 1 (autosomal dominant) Protein, Opa1 Protein, OPA1 Protein, opa1 Protein
- Sujet
- 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.
- Poids moléculaire
- 109.2 kDa
- NCBI Accession
- NP_570845
- Pathways
- Tube Formation
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