FTSJ1 (NM_012280) Human 3' UTR Clone
CAT#: SC208360
3' UTR clone of FtsJ homolog 1 (E. coli) (FTSJ1) transcript variant 1 for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | FTSJ1 (NM_012280) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CDLIV; JM23; MRX9; MRX44; SPB1; TRMT7 |
ACCN | NM_012280 |
Insert Size | 675 bp |
Sequence Data |
>SC208360 3' UTR clone of NM_012280
The sequence shown below is from the reference sequence of NM_012280. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CCCTGAGATGGAAGACAATGAAATGAGTTGTTCACCTTAACCCATTACGCTGGCAAACTGATACAACTCA GAAACTGCTCAATGTCAGGAAAACCGGAACTTGTTGATGAACTTGTTTTCAAAATATCATCTCATCAACG AGGCCTGGACAAACAAGCCCTGAGGAGGGATCTGCAACAACCCTGAAGACAACAAGGAAAGAAACCATGA AAGTCTGTCTGTACTGCAGTGGGAATTCTTGAGTGAGGTCTTACCTCTTCTTTAAACCTCTTCAGGAGTG TCCTGATTATGTCCAGAATTTTCCCTAAAGGCAGGGATTCTTAACCTGGATAGAAGCCAGGGGTAACCAT GAACTTGATGGAAGAAAATGTTACATCTTTATTTTCAGCAATGAAACTGAAATTTAGCCTTACTCCCAAG TTATAAATGCTGGCAACAAATCACAGTAGTAAAAGCAGTACCTGGGATTTTCCCACCAATACAAACCAGT TACAGCAACTGTAATGTAACATAAAAAGGGCATCTTGAAGTATTGTTCATATTTGTCACCTCTTGGAATG ATAGCAGATCCTGTAAGTTGATGTATTAATTAAAAAGCCCATATATTACTGCATCTCAATTTTGTTTCAA TTTAATATATAGTAATAATTGTAATTCAATGTAATTGGCTTCCAT ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_012280.2 |
Synonyms | CDLIV; JM23; MRX9; MRX44; SPB1; TRMT7 |
Summary | This gene encodes a member of the methyltransferase superfamily. The encoded protein localizes to the nucleolus, binds to S-adenosylmethionine, and may be involved in the processing and modification of ribosomal RNA. Mutations in this gene are associated with cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
Locus ID | 24140 |
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