D aspartate oxidase (DDO) (NM_003649) Human 3' UTR Clone

CAT#: SC208189

3`UTR clone of D-aspartate oxidase (DDO) transcript variant 1 for miRNA target validation


Reconstitution Protocol

USD 560.00

4 Weeks*

Size
    • 10 ug

Product Images

Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol DDO
Synonyms DASOX; DDO-1; DDO-2
ACCN NM_003649
Insert Size 591
Sequence Data
>SC208189 3'UTR clone of NM_003649
The sequence shown below is from the reference sequence of NM_003649. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

CCATTCCCAAGTCAAACCTGTAGATGACATAAAATGACAGCAAAGAGACTGAGAGACTGTTGATCAAAGC
ACAGAACAGGTTCAAATAACTTTTCCACTGCATGAAAGTTTAATTAGACATTTCTTTGTTTTCAACATTA
GAAGTGGTGTAACATGTAAGCTGAGCACGGTGGCATGCCTATAGTCCCAGCTACTTGAGAGGCTGAGGCA
GGAGGATTGTTGAGCCCAGGAGTTTGAGTGCAATCTGGGTAACATTTTTTAGAGGTGCCAGTTCCCACCT
CTAAAAAAAACACCAACAACAAAAGAAATGATGCAACATGTAGGCTTACTTAGGAAGTCCAGCATTAATG
GCATAGGGCATAAAGCTCTATTTTTTGTTAAAAATACTTCTTATAGAGTAAAATTTATTTAGAACTGATG
TCCAAGGACCTATGCAGATTTATATGAATGTTGGAAGCTATAGAGATTTTGATATCATTTGGCTTATAAA
TCCACAGGAGGAGATAATGTATGGAAAACATTTAAATCACTGTCAATTGCAGAGCTGCCTGTGATCTTCT
TAGGTTATAGCCAAGTCAGCAACATAATTCC

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_003649.2
Summary The protein encoded by this gene is a peroxisomal flavoprotein that catalyzes the oxidative deamination of D-aspartate and N-methyl D-aspartate. Flavin adenine dinucleotide or 6-hydroxyflavin adenine dinucleotide can serve as the cofactor in this reaction. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2019]
Locus ID 8528

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