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EYA1 Human shRNA Plasmid Kit (Locus ID 2138)

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SKU
TL304716
EYA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
In Stock*

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Other products for "EYA1 or NM_000503"

Specifications
Specifications
Product Data
Locus ID 2138
Synonyms BOP; BOR; BOS1; OFC1
Vector pGFP-C-shLenti
E. coli Selection Chloramphenicol (34 ug/ml)
Mammalian Cell Selection Puromycin
Format Lentiviral plasmids
Components EYA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 2138). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq NM_000503, NM_001288574, NM_001288575, NM_172058, NM_172059, NM_172060, NM_172059.1, NM_172059.2, NM_172059.3, NM_172060.1, NM_172060.2, NM_172060.3, NM_000503.1, NM_000503.2, NM_000503.3, NM_000503.4, NM_000503.5, NM_172058.1, NM_172058.2, NM_172058.3, NM_001288575.1, NM_001288574.1, BC121799, BC035138, BC048982, BC121798, NM_001370334, NM_001370335, NM_001370333, NM_001370336, NM_001288574.2, NM_000503.6, NM_001288575.2, NM_172058.4
UniProt ID Q99502
Summary This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript variants have been identified for this gene. provided by RefSeq, Dec 2013
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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