DGCR6 (NM_005675) Human 3' UTR Clone

CAT#: SC205803

3' UTR clone of DiGeorge syndrome critical region gene 6 (DGCR6) for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Cited in 1 publication.

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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 DGCR6 (NM_005675) Human 3' UTR Clone
Vector pMirTarget
ACCN NM_005675
Insert Size 429 bp
Sequence Data
>SC205803 3’UTR clone of NM_005675
The sequence shown below is from the reference sequence of NM_005675. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GACCAGAAAGGCAGCCCTGTCCCACCATAGCCACAGGCAGCAGAAGTCTGGGCAGAGTTCATCTTCTTG
ACCTTTGGCCACTGCCTTCCCAGCTGCCCGCAGGGGGTTCCCCCTGCTGAGGAGAGACCAGGTGGACCC
CAGCTGCCTGTCACCCTTCATCTGGGACTTGCTGTCAAACCCTAGGATAGTCTCATAAAGGGGAGGCTG
GGCCAGCCTGCTGCTGTCTGCTTCAGGGCCAGGCAGAGAGTGAGGCTGGGGGTTCTCACACCTTACTCC
ACCGGGCACATCCCAACCTGCACTGGGGCCCACTCGAGCGCTTGTTCTGGTCTCAGCCGCTCCCTTGGC
AGCTGCAGCCCCCATGCAGAAGAGGCTCCCAGGCCCAAGCTCTGTGTGACCCAGAGAAATAAAGATGCC
TCAGTGTGGCCCGCA
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_005675.6
Summary DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. The product of this gene shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the gamma-1 subunit of human laminin. This gene is a candidate for involvement in DiGeorge syndrome pathology and in schizophrenia. [provided by RefSeq, Nov 2008]
Locus ID 8214
MW 15.1
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Citations (1)

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