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Home TrueClone SOD1 Clone

SOD1 (NM_000454) Human cDNA Clone

Specifications Citations (3) Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC111022 SOD1 (untagged)-Human superoxide dismutase 1, soluble (SOD1) (10ug), NM_000454.4, 10ug $185 In Stock
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA500495 SOD1 (Superoxide Dismutase 1) mouse monoclonal antibody, clone 8B10, 100ul $379 In Stock
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Also for SOD1 (NM_000454)
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OriGene Data
Vector:pCMV6-XL5 Insert Size: 940 Restriction Site: NotI-NotI
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence          3' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: Druggable Genome
Protein Pathways: Amyotrophic lateral sclerosis (ALS)Huntington's diseasePrion diseases
Reference Data
RefSeq: NM_000454.4, NP_000445
RefSeq Size: 981 RefSeq ORF: 465
Synonyms : ALS; ALS1; HEL-S-44; homodimer; hSod1; IPOA; SOD
LocusID: 6647 Cytogenetic: 21q22.11 Domains: sodcu
Summary: 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, Jul 2008].


* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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