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
    • 10 ug

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DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
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CNY 1280.00

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
*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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