DISC1 (NM_001164539) Human 3' UTR Clone
CAT#: SC204766
3' UTR clone of disrupted in schizophrenia 1 (DISC1) transcript variant c 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 | DISC1 (NM_001164539) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C1orf136; SCZD9 |
ACCN | NM_001164539 |
Insert Size | 385 bp |
Sequence Data |
>SC204766 3’UTR clone of NM_001164539
The sequence shown below is from the reference sequence of NM_001164539. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGAGCCACTGTGCCTGGCCCCTACAATAATTCTTTAATGTGAGGAAATATCAAATGAAAAATAAGAAA TTCTAGGTAAGGAAAGAAATTTATTTAGTGGAAGTATAAAAGAAGTTTAAAAAGTTGAAGAAAATTTTG GTTTTCAATGTTGATGCAGCGTCCTTTGTGAATCTTTAAATTTGTGAATGACACTTTTGAAAACTTACA CCTTATTCTAAGTGTCTTTGTTCACTTTACACTGTACTGTAAAGAATCACAAGAGTGTCTCATAAATAA CTTTCTATATAACATATGTATATTTCAAAATAACATGTTATATATATAATACATACAATTTTTGTCAAT TAAACAGTACATTAAAAAGACAAAAATAACTTTCCATAAA 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_001164539.2 |
Synonyms | C1orf136; SCZD9 |
Summary | This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1;11)(q42.1;q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
Locus ID | 27185 |
MW | 15.2 |
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