NDUF3 (NDUFAF3) (NM_199073) Human 3' UTR Clone

CAT#: SC204353

3' UTR clone of NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 3 (NDUFAF3) nuclear gene encoding mitochondrial protein transcript variant 3 for miRNA target validation



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CNY 4,845.00


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 NDUF3 (NDUFAF3) (NM_199073) Human 3' UTR Clone
Vector pMirTarget
Synonyms 2P1; C3orf60; E3-3; MC1DN18
ACCN NM_199073
Insert Size 353 bp
Sequence Data
>SC204353 3’UTR clone of NM_199073
The sequence shown below is from the reference sequence of NM_199073. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CTTACATCTTTGGGCCAAGCTGCTCAATGAACCGCCAGGAACTGACCTGCTGACTGCACTCTGCCAGGC
TTCCCAATGCTTTCACTCTTATCTACCCTTTGGCACTTATCTTGCTTATCAACATAATAATTTATACAC
TTCTCCCATTTTGTATCAGGTGTGTTGCTGGCCAGGAGCTGATGGCTCACTGGGCTCTTGGAGGGGAAT
GTGAAGAAACCAAGGAGTCACTTTTTCATCTAGATTACTTAGGATTCCTTGACTTTTCAGAAGTCGGGA
AGCAGTATGTTTGCCTGTTGTAGACCTACTTGCTCACATGCAGATTTGAGAGGACCTCAACGGCTTTTC
TCACAAAA
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_199073.2
Synonyms 2P1; C3orf60; E3-3; MC1DN18
Summary This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]
Locus ID 25915
MW 12.9
*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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