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
Need custom modification / cloning service?
Get a free quote
CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
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 |
Documents
Product Manuals |
FAQs |
Resources
其它C1orf124产品
Customer
Reviews
Loading...