FANCL (NM_018062) Human 3' UTR Clone
CAT#: SC207278
3' UTR clone of Fanconi anemia complementation group L (FANCL) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | FANCL (NM_018062) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | FAAP43; PHF9; POG |
ACCN | NM_018062 |
Insert Size | 548 bp |
Sequence Data |
>SC207278 3’UTR clone of NM_018062
The sequence shown below is from the reference sequence of NM_018062. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACCTTAAAAATGTCTGGAAGGAAACACTGAAATAAGAATACAACATTTCGGTGAAGAGCTGGAAACTTA AAAAATTATCAAAAGGAATTTTGGTATCATCTTCAGAGAAAAAATAAAGCAAGAAATACTAACATCAAA AGGACAGGTATGATGATGCGATAATAATAAACATCTGCGTTTGTCTCTTCACTAAGAGTAAACTGGGAA ATTGTAGGCCAAAGTCCAGTTGAACTTTCTAAGTCTGTGATCCCCGTGCTGACTGTGGAAGTGTATTTA TACCAAGATGGAGATCTTGACTTCTTGAATATATCTGGACTGGTAAAATCTTGATGAGGCTCATAAAAT GAGTTTGGGAATTGTGTATAGCTGATTTTTTGTGGGAAACTGTTTACTTCATTCAAAGGTTCTTGAGAC TCTTGATATTTCTGTCTTCTCCTTGTGCTTTCCTATGGAAAAAATACATATATAGTTTAGTTTGTTAGA CGTGAGTTATCCAAGTATTTATTTTGTGTAGTGTGTAAGAATGCTAAATAAAATGTTATACAAGA 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_018062.4 |
Synonyms | FAAP43; PHF9; POG |
Summary | This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018] |
Locus ID | 55120 |
MW | 21 |
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