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Shox2 Mouse shRNA Plasmid (Locus ID 20429)

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SKU
TL502025
Shox2 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
2 Weeks*

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Other products for "Shox2 or NM_001302357"

Specifications
Specifications
Product Data
Locus ID 20429
Synonyms 6330543G17Rik; OG12; Og12x; Prx3; SHOT
Vector pGFP-C-shLenti
E. coli Selection Chloramphenicol (34 ug/ml)
Mammalian Cell Selection Puromycin
Format Lentiviral plasmids
Components Shox2 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 20429). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq NM_001302357, NM_001302358, NM_001302359, NM_013665, NM_013665.1, NM_001302358.1, NM_001302359.1, NM_001302357.1, BC172634
UniProt ID P70390
Summary May be a growth regulator and have a role in specifying neural systems involved in processing somatosensory information, as well as in face and body structure formation. May also have a role in heart development.UniProtKB/Swiss-Prot Function
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
Shipping Ambient
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Documents
Resources

file-alt Citations

Shox2 regulates progression through chondrogenesis in the mouse proximal limb
Bobick, Cobb
J. Cell. Sci. (2012) 125 (Pt 24), 6071-83 DOI: 10.1242/jcs.111997
Cited by 59
AI Summary: OriGene products, specifically the Shox2 shRNA (OriGene, TL502431) and Shox2 cDNA clone (OriGene, MR206307), were used in this study to manipulate Shox2 expression in cell culture experiments, enabling the authors to investigate the gene’s role in regulating chondrogenesis and chondrocyte maturation.
Snippet: Author for correspondence (jacobb{at}ucalgary.ca). Next Section. Summary. In humans, loss of SHOX gene function is responsible for the mesomelic short stature characteristic of Turner syndrome, Leri-Weill dyschondrosteosis, and Langer dysplasia.
Showing 1-1 of 1 papers.
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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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