EHMT1/GLP (EHMT1) (NM_001145527) Human 3' UTR Clone
CAT#: SC203263
3' UTR clone of euchromatic histone-lysine N-methyltransferase 1 (EHMT1) transcript variant 2 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 | EHMT1/GLP (EHMT1) (NM_001145527) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | EHMT1-IT1; Eu-HMTase1; EUHMTASE1; FP13812; GLP; GLP1; KLEFS1; KMT1D |
ACCN | NM_001145527 |
Insert Size | 273 bp |
Sequence Data |
>SC203263 3’UTR clone of NM_001145527
The sequence shown below is from the reference sequence of NM_001145527. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCCCAAGGTCGAGGGGCTGCCTTTGGTGACTTATGGTGAGGACCTCGTGCTGTTCCCGAACACAGCCA GGAACCACGCCAAGAGGAAGATGCTCCAGCACAGCCTTGCTGTGGACCAGGCCGCCCACAGGGAGCAGG TCCATTCCTGGGGGCTGACTCCGCCTTTCAGAGAGGCGTGGCTCCATCTTCACAGCCTCGTAGCCTCTT AAAGGCCCAGCCTCAAAACCTCATTGGGGCCCCCAGCCCCGGTAAATAAATTGCATTCAGACCATA 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_001145527.2 |
Synonyms | EHMT1-IT1; Eu-HMTase1; EUHMTASE1; FP13812; GLP; GLP1; KLEFS1; KMT1D |
Summary | The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017] |
Locus ID | 79813 |
MW | 9.9 |
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