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
    • 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 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
*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.

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