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
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

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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