Supersoxide Dismutase 1 (SOD1) Muismonoklonale Antilichaam [Kloon ID: LBI8B10]

The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq]

Carrier-free (BSA/glycerol-free) SOD1 mouse monoclonal antibody, clone LBI8B10

ALS; ALS1; HEL-S-44; homodimer; hSod1; IPOA; SOD

Homo sapiens superoxide dismutase 1 (SOD1), mRNA.

6647

P00441

Unconjugated

Amyotrophic lateral sclerosis (ALS), Huntington's disease, Prion diseases

Amyotrophic lateral sclerosis (ALS), Huntington's disease, Prion diseases

WB 1:1000~2000, IHC 1:50, FLOW 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

SOD1

https://www.ncbi.nlm.nih.gov/gene/?term=6647

https://www.uniprot.org/uniprot/P00441