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CCNQ (NM_001130997) Human 3' UTR Clone

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SKU
SC206170
3' UTR clone of family with sequence similarity 58 member A (FAM58A) transcript variant 2 for miRNA target validation
  $683.00
4 Weeks*
Size
Bulk Requests & Clone Modifications

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Specifications
Specifications
Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Target Symbol CCNQ
Synonyms CycM; FAM58A
ACCN NM_001130997
Insert Size 470 bp
Sequence Data
Insert Sequence
>SC206170 3’UTR clone of NM_001130997
The sequence shown below is from the reference sequence of NM_001130997. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
ATTTATACCATGGACACAGAGATCCCCTAAGGTCCTGGCCCAGGCCTGCCCAAAGAGAAGCCCAGGATG
GTCGGCTGCCTGGGGACATTGTCACCACGTCGCCATGACGGCTGGTCCCCACAGGACCAGCTGGGAGGA
CTGGTTGTGCTGCTGGAGAAGGGCTGGAGAAGGCAATGGCATGCTGCCGCTTTGCCAGTCCCTAGAAGT
CGCGGTGCAGGTGATGGTGGGAGCCGCGCCTCCAGCGGGCAGGCCGGGAGTGTACTGTGTGCAGCTGAC
CCAAGGCAGCCACATCTGCGTTTGTCCTTTGAGAGGACTTTGACTACAATACAGGCATGACATCAATGA
AAGGAAAGTCATGAAATCGATGAGACTGAATCCCTACGGATTTCTTAAAAGCCAGATTTGTAGGGAGAA
TGAATGTGCAACGTGGCTGAAATCTATTTTGTGTAATAAAAGGTGATACAAGTCAA
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).
Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Shipping Ambient
Reference Data
RefSeq NM_001130997.3
Locus ID 92002
Summary Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. provided by RefSeq, Oct 2008
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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.