FAM111A (NM_001142519) Human 3' UTR Clone
CAT#: SC215231
3' UTR clone of family with sequence similarity 111 member A (FAM111A) transcript variant 4 for miRNA target validation
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CNY 5,795.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | FAM111A (NM_001142519) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | GCLEB; KCS2 |
ACCN | NM_001142519 |
Insert Size | 1565 bp |
Sequence Data |
>SC215231 3’UTR clone of NM_001142519
The sequence shown below is from the reference sequence of NM_001142519. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTAGAAATGATGAGTGATGAGGACTTGTGAGAATTCAGTCTACTGGATTTAAGGGAATGGCTTATGGAG TTGTTATTTCATAGGCATTGAAAATGGTTTTCTAAACTCCAAAATGGTCATCTTATCAATAATAATAAT ATTGACCATTTCCTATCTGCCAGGCATTTTTCTAAGCACATGAAGAAATTAGTCCTAACAACACTATGA GATGGACTATAACTTGCCCAAATTTTTTTTTTTTTTTTGAGACTGAGTCTCACTCTGTCGCCTGGGCTG GAGTACAGTGGTGCGATCTCAGCTCACTGCAACTTCCACCTCCCAGGTTCAAGCGATTCTTATGCCTCA GTCTCCTGAGCAGCTGGGATTACAGGCAAACGCCACCACACCCAGCTAAATTTTTTTTTTTTTTTTTGT ATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCGGGTCTCGAACTCCTGACCTCGTGATCCAC CTGCCTCGGCCTTCCAAAGTGCTGGGATTACAAGTTTGAGCCACTGCACCTGGCTAACTTGCCCTATTT TAAAGTCAAGCAATGGGAAGAATAACAAGATTATATAGTAATCAGTTTCATGACACTAAAAGTCATATA GTCATAGGGTTTTTTCATCTTTCATATCTTTGCCTAAATTCATTTGCTACAGTGCAGGAACCAAAACTT GTTCATCTCATGATTCCCTACATCTGACATAAGGAAAGTAAGTGCTCAGAAAAATGTGCAGGTCAATAA GTTGCAAAAGTTGGGGCTGCAATTAATGCTAACATAAGAGCTAAATGCTTGATTAGAAATGATCTCAAA ACCTTTTAGAATTTCCAAAATCTTCATATTACTGAAACTGTCGGAATATATGGGTCTTGAAATTCAGAA GATGATAGTCACTCTTCCCATATTTATAGGCTATTAAGGCAAGGGATATCTTAAACATCATATTACTTT ATTTAGATTTCTACTACTCCAATTATTAATGTTATGTATTTCTCATTGTTTTACTTCTTCATGGTATTA TGAAGACTATATAGATGATTCAACCAAGCCTGCAAATCTCCCTCTTGTGGAATTCCACTGGACCCAATC TGTTTTCCATTTCCATTGCAATACTACTAAAGCCATACAATATCAAGCACCCTCCCTCTAGGTCCAGGG ACTATCACAGAAGAAGCAGGCATGTAAGATTTTAAGGACTGGTTTCGAGGGGTCGAGTGTAGGAAAACA GCCTGTTGCATTGTAAGAGTGATGTCATCTTGAAGAGCAGCTGGCATGATGACTGCTGTTTGACTCCTG CATACCAAGATATTCTGCAGCAATGTCTTTAAACAGTGCCGGTAGTACAGATAACCCCTCATAAAGATG CTTATCTAACCTCCCCAGTGTTCAGGTGTTTCACAAGAAAGTCTGAGATATGACTAGCTACACGTTTTG CCAAAAATGCTTGTTATATAAAGGGTACTTTTGGGAGGGTGAGTGCCGCCATTTAGTGGCTGCTAGAAA CATTGCTTCTGTTTGTAAGTTCCTATTAAATGTTTCTTTCTGAGAAA 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_001142519.3 |
Synonyms | GCLEB; KCS2 |
Summary | The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
Locus ID | 63901 |
MW | 59.3 |
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