NMDAR2A (GRIN2A) (NM_001134408) Human 3' UTR Clone

CAT#: SC208951

3' UTR clone of glutamate receptor ionotropic N-methyl D-aspartate 2A (GRIN2A) 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 NMDAR2A (GRIN2A) (NM_001134408) Human 3' UTR Clone
Vector pMirTarget
Synonyms EPND; FESD; GluN2A; LKS; NMDAR2A; NR2A
ACCN NM_001134408
Insert Size 2000 bp
Sequence Data
>SC208951 3’UTR clone of NM_001134408
The sequence shown below is from the reference sequence of NM_001134408. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
ACAAACACTCGTTGCCATCCCAGGCGGTGAATGACAGCTATCTTCGGTCGTCCTTGAGGTCAACGGCAT
CGTACTGTTCCAGGGACAGTCGGGGCCACAATGATGTGTATATTTCGGAGCATGTTATGCCTTATGCTG
CAAATAAGAATAATATGTACTCTACCCCCAGGGTTTTAAATTCCTGCAGCAATAGACGCGTGTACAAGA
AAATGCCTAGTATCGAATCTGATGTTTAAAAATCTTCCATTAATGTTTTATCTATAGGGAAATATACGT
AATGGCCAATGTTCTGGAGGGTAAATGTTGGATGTCCAATAGTGCCCTGCTAAGAGGAAGAAGATGTAG
GGAGGTATTTTGTTGTTGTTGTTGTTGGCTCTTTTGCACACGGCTTCATGCCATAATCTTCCACTCAAG
GAATCTTGTGAGGTGTGTGCTGAGCATGGCAGACACCAGATAGGTGAGTCCTTAACCAAAAATAACTAA
CTACATAAGGGCAAGTCTCCGGGACATGCCTACTGGGTATGTTGGCAATAATGATGCATTGGATGCCAA
TGGTGATGTTATGATTTCCTATATTCCAAATTCCATTAAGGTCAGCCCACCATGTAATTTTCTCATCAG
AAATGCCTAATGGTTTCTCTAATACAGAATAAGCAATATGGTGTGCATGTAAACCTGACACAGACAAAA
TAAAAACAGTTAAGAATGCATCTGCACTGTAGTGCGATTGACATGTGCAAGAGATTAGGAAGTTTGGCT
CGTAACAGTTTCAGCTTTCTTGTTATGCCTTCCATCACAGCCCAGGCTCACCCCAAGAACTCCAGGCTC
CCCTAAAGAATAGCAAATCAGTGTGTTCGTGATGACTGTGCTACCTTCATTATAGTTCATTTCCAAGAC
ACATCTGGAGCCAAAGGCCCGAGGGACCCTCAGGTGGGGAGAGCTACAGGAATCTCTTTGGATGTTGAT
GTGTGTTTCTCTCACCCTCGGCTTCGATGGTCTTGTTCAGAGCTGCATAAACTAACACATTTATGTCTC
CGAGATCTAAGTGTGGATCTTCTGTCTGTGACACAGTGGCCATTGTAGTTTATCCCGAAGACGCCTATG
TACGTAAGTTTGCATTTCCTCCCTTCTGGTGATGACTCAGGGTTGTATAGTATCTGTTACCCCTTCCCT
CCCAGAGTAACCATAACTCGTTCCGTTTCCAAACAGCCATGGTGGTGTCCAATTAGCTGTGTATCGCTC
TTCCCAGAGTTGTTAATGTGGTGACATGCACCAACAGCCGTATGTGTACTGTGATCTGTAAGAAGTACA
ATGCCATCTGTCTGCCGAAGGCTAGCATGGTTTTAGGTTTATCTTCCTTCACATCCAGAAATTCTGTTG
GACACTCACTTCCACCCCAAACTCCTCAAATCAAAAGCCTTCAAAACACGAGGCACTCTTGGATCTACC
CTGAGTATCCTCCAAACTGTGGATACAGTTTAGTGAGACAAGCAATTTCTCCCTTCTGAGTTATTCTCT
CTGTTGGTGGCAAACCACTTCATAGCACCAACAGAGATGTAGGAAAAATTCCTCAAAGTATTTGTCATT
TCTGAGTCGCCTGCATTATCCCATTCTTATTCTCCTCAAACCTGTGCATATATGACATGAAATGATATC
CATTTTTTTTTTAAGTTAGAGACAGAGAGGGGAATACTTATGCATGGGGAGCCTGTTAGCACAGTGCCT
GCCACAAAAACAAGTGCCCCCGACAAGATAGTTGCTATGTTATGACACTTTCTCAGATCAGGATTTTCT
AGTTTAAAAATTAAATATCATAAAACCAGCAAATAATATTAACTAAACCTTTTATATAGTTCTACTCTG
TTAATTAGTGTATTTCATGTACATGAATATTTTTGAAGTATTTGGGATAACTAGCCATCAGTGTTTGCA
GAAGACCTCAGTCTGTTTTGGGCCATTACGGAAACACTAAGCTAATGTAGACTCGCCTGGCCATTTCC
AGCGGACCGACTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCC
CAACCTGCCATCACGAGATTTCGATTCCACCGCCGC
Restriction Sites SgfI-RsrII     
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_001134408.2
Synonyms EPND; FESD; GluN2A; LKS; NMDAR2A; NR2A
Summary This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
Locus ID 2903
MW 75.5
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