OPA1 Human shRNA Plasmid Kit (Locus ID 4976)

SKU
TL302801
OPA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
In Stock*
Specifications
Specifications
Product Data
Locus ID 4976
Synonyms BERHS; largeG; MGM1; MTDPS14; NPG; NTG
Vector pGFP-C-shLenti
E. coli Selection Chloramphenicol (34 ug/ml)
Mammalian Cell Selection Puromycin
Format Lentiviral plasmids
Components OPA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 4976). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq NM_015560, NM_130831, NM_130832, NM_130833, NM_130834, NM_130835, NM_130836, NM_130837, NM_001354663, NM_001354664, NM_015560.1, NM_015560.2, NM_130831.1, NM_130831.2, NM_130832.1, NM_130832.2, NM_130834.1, NM_130834.2, NM_130837.1, NM_130837.2, NM_130835.1, NM_130835.2, NM_130833.1, NM_130833.2, NM_130836.1, NM_130836.2, BC075805, BC075805.1, BC035393, BC043443, BC058013, NM_130837.3, NM_130832.3, NM_130834.3, NM_130833.3, NM_130836.3
UniProt ID O60313
Summary The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. 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. provided by RefSeq, Aug 2017
shRNA Design These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
Storage Store at -20°C
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