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Over 1000 citations of OriGene cDNA clones
MET Receptor Sequence Variants R970C and T992I Lack Transforming Capacity Cancer Res., Aug 2010; 70: 6233 - 6237 [MET]

Methyl 2-Cyano-3,12-dioxooleana-1,9-dien-28-oate Decreases Specificity Protein Transcription Factors and Inhibits Pancreatic Tumor Growth: Role of MicroRNA-27a Mol. Pharmacol., Aug 2010; 78: 226 - 236 [ZBTB10]

Tumor Lymphangiogenesis and Metastasis to Lymph Nodes Induced by Cancer Cell Expression of Podoplanin Am. J. Pathol., Aug 2010; 177: 1004 - 1016 [PDPN]

AML1 is overexpressed in patients with myeloproliferative neoplasms and mediates JAK2V617F-independent overexpression of NF-E2 Blood, Jul 2010; 116: 254 - 266 [RUNX1]

View All Citations >>

SETD2 (NM_014159) Human cDNA Clone

Specifications Related Products Product Manual FAQs
Cat. No. Ref. ID Description Amount Price Shipping  
SC115150 NM_014159 Homo sapiens SET domain containing 2 (SETD2) as transfection-ready DNA NM_014159.3 $4100 Next day Add to Shopping Cart


OriGene TrueClone Data
Vector:pCMV6-XL4 Insert Size: 6300 Restriction Site: NotI-NotI
Sequence Data: 5' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Reference Data
RefSeq: NM_014159.3, NP_054878
RefSeq Size: 7311 RefSeq ORF: 6186
Synonyms : FLJ16420; FLJ22472; FLJ23184; FLJ45883; FLJ46217; HBP231; HIF-1; HSPC069; HYPB; KIAA1732; KMT3A;
LocusID: 29072 Cytogenetic: 3p21.31 Domains: WW, SET, PostSET, AWS
Summary: Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein belonging to a class of huntingtin interacting proteins characterized by WW motifs. This protein is a histone methyltransferase that is specific for lysine-36 of histone H3, and methylation of this residue is associated with active chromatin. This protein also contains a novel transcriptional activation domain and has been found associated with hyperphosphorylated RNA polymerase II. [provided by RefSeq].

Transcript Variant: This variant (1) encodes the longer isoform (1).

Insert Size determined experimentally by digestion of the clone with Not I restriction enzyme

 

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