SOD2 (NM_000636) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC202330L2V

  • LentiORF®

Lenti ORF particles, SOD2 (mGFP-tagged) - Human superoxide dismutase 2, mitochondrial (SOD2), nuclear gene encoding mitochondrial protein, transcript variant 1, 200ul, >10^7 TU/mL

  View "NM_000636" in other vectors (11)

USD 930.00


Availability*
6 Weeks

Size
    • 200 ul


Product images

Specifications

Product Data
Product Name SOD2 (NM_000636) Human Tagged ORF Clone Lentiviral Particle
Symbol SOD2
Synonyms IPOB; MNSOD; MVCD6; IPO-B; Mn-SOD
Vector pLenti-C-mGFP
ACCN NM_000636
ORF Size 666 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC202330).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Product Components The ORF clone is ion-exchange column purified, transfection-ready dried plasmid DNA, and shipped with 2 vector sequencing primers.
Reference Data
RefSeq NM_000636.2, NP_000627
RefSeq Size 1593
RefSeq ORF 669
Locus ID 6648
Cytogenetics 6q25.3
Domains sodfe
Protein Families Transcription Factors, Druggable Genome
Protein Pathways Huntington's disease
MW 24.75 kDa
Gene Summary This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. [provided by RefSeq, Apr 2016]

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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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