DISC1 (NM_001164554) Human 3' UTR Clone

CAT#: SC207063

3`UTR clone of disrupted in schizophrenia 1 (DISC1) transcript variant q for miRNA target validation


Reconstitution Protocol

USD 560.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol DISC1
Synonyms C1orf136; SCZD9
ACCN NM_001164554
Insert Size 543
Sequence Data
>SC207063 3'UTR clone of NM_001164554
The sequence shown below is from the reference sequence of NM_001164554. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

GGAAGATGCAGTTGAGAATGATGATTATGATAAAGGTGAGTTTTAATTTGTTTATTGATTGTTTTGTCAT
CATGTCCCAATTTTCTTTCCATCTTTACTCATATCTACCTTTTGAATCCCAAAAGAATTGTACAATCTGT
TCCTCTGATCATCTCTACCAGGGAATAGTTGACTCTTTTACAGCATTATTGTTTTGTAGATTTCAAAGTA
CTTCATGAACATTAATCCTTTGGGTTATAAATATAACCTTATCAATTGTCCAGAAACACTTAGCATACTC
ACACAATAAAAATTATATTAGCTTGCCACCTGTCTGCCCATGGTGTGATGTATCTATAATCCACTTGTTC
ATAAAAAATATTCGTCTGACACCTATGATATGCTAGGGAATATGGGAGACAATAGGAAAGTAAGACAGAC
ATGGTATCTGCCCTTGTGATGCCAGTAAACTTAAGCCTTCATGGGGCTCTCTGACTTCATAATTTCCAGA
ACCAGAGATAGGAAATGAGGTGAATTTGAGAAATGTCAGACTGTGCCAAAGGG

ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_001164554.1
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

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