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OPA1 Rabbit Polyclonal Antibody (Biotin)

CAT: 0013-GTR18564499Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18564499Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
OPA1 Rabbit Polyclonal Antibody (Biotin)
Product Name Alternative
Dynamin-like 120 kDa protein, mitochondrial; 3.6.5.5; Optic atrophy protein 1; Dynamin-like 120 kDa protein, form S1; OPA1; KIAA0567
UniProt
O60313
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
A synthetic peptide corresponding to a sequence at the C-terminus of human OPA1, different from the related mouse and rat sequences by one amino acid.
Target
Dynamin-like GTPase OPA1, mitochondrial
Clonality
Polyclonal
Conjugation
Biotin
Field of Research
Cardiovascular Research, Metabolism Research, Neuroscience
Purification
Immunogen affinity purified.
Dilution
Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
111631 Da
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
Notes
For research use only.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · O60313

Dynamin-like GTPase OPA1, mitochondrial

OPA1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O60313
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
OPA1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.6.5.5
Processing
Precursor
Secondary accessions
D3DNW4, E5KLJ5, E5KLJ6, E5KLJ7, E5KLK1, E5KLK2
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationDisulfide bond

Coding sequence diversity

Alternative splicing

Biological process

ApoptosisSensory transductionVision

Disease

CardiomyopathyDeafnessDisease variantNeurodegenerationPrimary mitochondrial disease

Domain

Coiled coilTransit peptideTransmembraneTransmembrane helix

Ligand

GTP-bindingLipid-bindingNucleotide-binding

Molecular function

Hydrolase

Cellular component

MembraneMitochondrionMitochondrion inner membrane

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