EPM2A (NM_001018041) Human 3' UTR Clone

CAT#: SC205379

3' UTR clone of epilepsy progressive myoclonus type 2A Lafora disease (laforin) (EPM2A) transcript variant 2 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 EPM2A (NM_001018041) Human 3' UTR Clone
Vector pMirTarget
Synonyms EPM2; MELF
ACCN NM_001018041
Insert Size 420 bp
Sequence Data
>SC205379 3’UTR clone of NM_001018041
The sequence shown below is from the reference sequence of NM_001018041. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GCAGCTAGCCAGGACACATTTCCACTATAATTTTACAAAGTTAAATTTATAAGCTAGCATTAAGTAAAG
TGAAGTCCAGCTCCCTTGCTAAAAATAACTAGAGGTAATAATTGGTATTCAGGTAACTCATTTACAGTC
ATAATGTGTTGTGAAAATTTAATCTTAAAAATTAAATTTTTAAACTATGTGGGTCTGTGAATTTCTTTA
ATGTCTAAGAAATCCAGCTTCATAATTTCCATGATACAAAGATCTTTTTTCAGGTGGATTTTTACCTTT
GTTCCTTTTGCTCTGATAGACAAAATCAGTTTAGGACTATTAAAGAATGTTTTGGAATAAACTGTCTTT
TTCCTCAATGAATGGGATGTCTAATGTATTTCAAAATCACCCAAAACTTTTGGCAAATAAAAGCATTTA
AAAAGA
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_001018041.2
Synonyms EPM2; MELF
Summary This gene encodes a dual-specificity phosphatase and may be involved in the regulation of glycogen metabolism. The protein acts on complex carbohydrates to prevent glycogen hyperphosphorylation, thus avoiding the formation of insoluble aggregates. Loss-of-function mutations in this gene have been associated with Lafora disease, a rare, adult-onset recessive neurodegenerative disease, which results in myoclonus epilepsy and usually results in death several years after the onset of symptoms. The disease is characterized by the accumulation of insoluble particles called Lafora bodies, which are derived from glycogen. [provided by RefSeq, Jan 2018]
Locus ID 7957
MW 16.2
*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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