C1orf124 (SPRTN) (NM_032018) Human 3' UTR Clone

CAT#: SC210946

3' UTR clone of chromosome 1 open reading frame 124 (C1orf124) transcript variant 1 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 C1orf124 (SPRTN) (NM_032018) Human 3' UTR Clone
Vector pMirTarget
Synonyms C1orf124; DVC1; PRO4323; spartan
ACCN NM_032018
Insert Size 1692 bp
Sequence Data
>SC210946 3’UTR clone of NM_032018
The sequence shown below is from the reference sequence of NM_032018. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
ATCAAAGTCAAAAGCGAAGAAAGTCTTTGAAAAAGGTTTCAAAGTCTCAAGTACCACCTGTATTATCTC
ACTAATGTGCTATGTCAGCCAGTCAGGAAGTTCTGGTTAATACTAAGATTTGTAGGTTATAATCTAGTT
CACATAACCAATAGAAAGTGTCCTATTTTATATATACGCATATAAGATTGTAATTTTAAGATGTTTTGT
GTCTCAGGGTGCTACATTCACTCTTGCCTTAGGTATACTGTAACCCAGGTTCTGCCTGTCGTGTATAAG
TTTTAGATACTTTTGTTCTTTCTTGCTCTTAAGGATTTTAAAAACCTGTTAATCTTTTTATTTGTATAC
TTTCCTAAAAATATTCATATGGGGAATCCTGTCAGGTGTTTGGTTATATTGACTATTTATTAATAGTAT
TAGAACTCATTCCCTGAACTGATGTAAATCTTCATAGTGTCAGACATACTGACCAAAACCACAATCTAG
ACTACAAAGTATATTGTTTTAGAGTACTCAAATTGTATTATTTATTAATTTTTTTGTTTGCAAAATCTT
AACAGGAACTGTATTTTCTATATTTTAAAGAATTTTATTTGTCCCACTTTTACTAAACAGTGGCAGCAG
ATTTTAAGTTAAAGAATATGGAATATAGTAAAATAAGTAAATTTCTTTTGGAATATTTTTAGTAACAAA
TAGCCACTATAATTCTGTAGGCCAAATTTTATATTGAGTTTAGCTGTTTTCTCAAAATTTAGCAGAGTG
GTTAAAATTCTGTGCTGATAAGTAACTGATACATATAACATAAACATAACAAAGTTGCCTAGTTGATGT
AACAGTGGAAAGTTATCTGGAAATAGTATTTTGAACTTTAAGCCAAGTTTAAAACATTATAATAAAAGG
AATACCATTTGTGCATTTTAAGTAATCTTTTTTAAAAAAAATATTTTCCATGTTATAGGGAAAGGACAA
AGAGACTTTTATCAGTTTGCTTTTTGTCTTGTGGCTGTACATGCTGTTGGCATAGCCCTAACACAGTTG
TTCACAAGTTTTCTTTTTTCTTGTTGCAATTTTCCTTCACTTTGTTGTAATACAGGTGCACAAATCTTA
AGTGCACAGCTGGGTAAACTTTTACAGTGTTCACCTGTGTAACTACCACCCGGATCAAGTTAGAGAACA
CTTCCATTGCCACAGAAGGCTTCCTATAGGTGTCTGTTCCCAGTTGATACCCATGACCCTCACCACCTC
CAGAGGTCCCCACTGTTTTCACCCCATCGTCGCAGATTATTTTTTAATTTTATAATGTAGTATCTTTGT
TCCTATGTATAGCAGGAGTTCATTTTCATTGCTCTTGCATTTGTATGAATATACTAGAATTTATTCATC
CATTCTAATGTTAATGGACATTTGAATTATTTCCAGTTTGGGGCTGTTAAGCATAATGCTGCTAAGAAC
ATTCTTATCTTTTCTGTTGGGTATATATACAGGAATGGAATTGCTGAGTCACGGGGTATATTTCTGTTT
AGCTTTAGTAAATTCTGCCAGTTTACACTCCTACCAGCAATGTATGAGAGTTTTAGTTGTTCACCATTC
ATAACACTGTTAGCAGCCCTTTTCGTTTTAGACTGGTTGGCTGTTCACAAATTTTGATATTCCTTAAAG
CATTAAAACATTTTAATAAATACTTATAAATAGGTA
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_032018.7
Synonyms C1orf124; DVC1; PRO4323; spartan
Summary The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
Locus ID 83932
MW 66
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