NMDAR2C (GRIN2C) (NM_000835) Human 3' UTR Clone

Specifications

Product Data
Product Name	NMDAR2C (GRIN2C) (NM_000835) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GluN2C; NMDAR2C; NR2C
ACCN	NM_000835
Insert Size	442 bp
Sequence Data	Insert Sequence (showhide) >SC205926 3’UTR clone of NM_000835 The sequence shown below is from the reference sequence of NM_000835. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGGATCTCCAGTCTGGAGTCAGAAGTGTGAGTTATCAGCCACTCAGGCTCCGAGCCAGCTGGATTCTCT GCCTGCCACTGTCAGGGTTAAGCGGCAGGCAGGATTGGGCTTTTCTGGCTTCTGCCATGAAATCCTGGC CATGGGACCCCAGTGACAGATGATGTCTTCCATGGTCATCAGTGACCTCAGTAGCCTCAAATCATGGTG AGGGCTGGGCTTTTGCTGTCCTCTTCTCACGCAGAGTTCTGCCAGGAGGGTGTGCTGTGGGGGTCAGAC TCCTGAGGCTCTCCCTTCCCTGGGGCTAGCCAGTTACTGGTCATGGCTGCTGTGGGCATGGAGGCTGGA ACTTGTGGTTGAGGCAGGGCCATCCCGATCCTTGCTCTACCTGGCTAGAGTTTCTTCTCATCAGAGCAC TGGGACATTAAACCAACCTTTTACAACA 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_000835.6
Synonyms	GluN2C; NMDAR2C; NR2C
Summary	This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D), forming a channel that is permeable to calcium, potassium, and sodium, and whose properties are determined by subunit composition. Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease, Alzheimer's disease, depression, and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]
Locus ID	2905
MW	15.5

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