HTRA1 Human siRNA Oligo Duplex (Locus ID 5654)
CAT#: SR303800
HTRA1 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each
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CNY 4,090.00
货期*
4周
规格
Cited in 1 publication. |
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经常一起买 (3)
Specifications
Product Data | |
Purity | HPLC purified |
Quality Control | Tested by ESI-MS |
Sequences | Available with shipment |
Stability | One year from date of shipment when stored at -20°C. |
# of transfections | Approximately 330 transfections/2nmol in 24-well plate under optimized conditions (final conc. 10 nM). |
Note | Single siRNA duplex (10nmol) can be ordered. |
Reference Data | |
RefSeq | NM_002775 |
Synonyms | ARMD7; CADASIL2; CARASIL; HtrA; L56; ORF480; PRSS11 |
Components | HTRA1 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each (Locus ID 5654)Included - SR30004, Trilencer-27 Universal Scrambled Negative Control siRNA Duplex - 2 nmolIncluded - SR30005, RNAse free siRNA Duplex Resuspension Buffer - 2 ml |
Summary | This gene encodes a member of the trypsin family of serine proteases. This protein is a secreted enzyme that is proposed to regulate the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins. It has also been suggested to be a regulator of cell growth. Variations in the promoter region of this gene are the cause of susceptibility to age-related macular degeneration type 7. [provided by RefSeq, Jul 2008] |
Performance Guranteed | OriGene guarantees that at least two of the three Dicer-Substrate duplexes in the kit will provide at least 70% or more knockdown of the target mRNA when used at 10 nM concentration by quantitative RT-PCR when the TYE-563 fluorescent transfection control duplex (cat# SR30002) indicates that >90% of the cells have been transfected and the HPRT positive control (cat# SR30003) provides 90% knockdown efficiency. For non-conforming siRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the siRNA kit. To arrange for a free replacement with newly designed duplexes, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled siRNA control (quantitative RT-PCR data required). |
Citations (1)
The use of this RNAi has been cited in the following citations: |
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The genomic landscape of schwannoma
,Agnihotri, S;Jalali, S;Wilson, MR;Danesh, A;Li, M;Klironomos, G;Krieger, JR;Mansouri, A;Khan, O;Mamatjan, Y;Landon-Brace, N;Tung, T;Dowar, M;Li, T;Bruce, JP;Burrell, KE;Tonge, PD;Alamsahebpour, A;Krischek, B;Agarwalla, PK;Bi, WL;Dunn, IF;Beroukhim, R;Fehlings, MG;Bril, V;Pagnotta, SM;Iavarone, A;Pugh, TJ;Aldape, KD;Zadeh, G;,
Nat. Genet.
,PubMed ID 27723760
[HTRA1]
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