SETD2 (NM_014159) Human 3' UTR Clone
CAT#: SC209106
3' UTR clone of SET domain containing 2 (SETD2) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | SETD2 (NM_014159) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | HBP231; HIF-1; HIP-1; HSPC069; HYPB; KMT3A; LLS; p231HBP; SET2 |
ACCN | NM_014159 |
Insert Size | 687 bp |
Sequence Data |
>SC209106 3’UTR clone of NM_014159
The sequence shown below is from the reference sequence of NM_014159. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAACCCAAAGAGGACACTGAATTAGAGTGACTGTTGGGCCAGGGTGGGAGGATGGGTGGTCAGGTAAGA CAGACTCTAGGGAGAGGAAATCCTGTGGGCCTTTCTGTCCCACCCCTGTCAGCACTGTGCTACTGATGA TACATCACCCTGGGGAATTCAACCCTGCAGATGTCAACTGAAGGCCACAAAAATGAACTCCATCTACAA GTGATTACCTAGTTGTGAGCTGTTGGCATGTGGTTAGAAGCCATCAGAGGTGCAAGGGCTTAGAAAAGA CCCTGGCCAGACCTGACTCCACTCTTAAACCTGGGTCTTCTCCTTGGCGGTGCTGTCAGCGCACAGACC CATGCGCATCCCCACCCACAACCCTTTACCCTGATGATCTGTATTATATTTTAATGTATATGTGAATAT ATTGAAAATAATTTGTTTTTTCCTGGTTTTTGTTTGGTTTTCGTTTTGCTTTTAGCCTCTACATGCTAG GATCACAGGAAGACTTTGTAAGGACAGTTTAAGTTCTCCTGCAAGGTTTAATTTGTTATCATGTAAATA TTCTAAAGCAGGCTGCCTTGTGGTTTTGGCCAGCCTTGTGCTATGTTGATAAGATTGATTTACTGCTTA AAATCACTTTACTTTATCCAATTTTTACTGAACTTTTTATGTAAAAAAATAAAATCAATTAAAGAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_014159.7 |
Synonyms | HBP231; HIF-1; HIP-1; HSPC069; HYPB; KMT3A; LLS; p231HBP; SET2 |
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, Aug 2008] |
Locus ID | 29072 |
MW | 25.7 |
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