GRIK1 (NM_175611) Human 3' UTR Clone
CAT#: SC204023
3' UTR clone of glutamate receptor ionotropic kainate 1 (GRIK1) transcript variant 2 for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | GRIK1 (NM_175611) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | EAA3; EEA3; GLR5; GluK1; gluR-5; GLUR5 |
ACCN | NM_175611 |
Insert Size | 327 bp |
Sequence Data |
>SC204023 3’UTR clone of NM_175611
The sequence shown below is from the reference sequence of NM_175611. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGAACTCAGAGAAAAGAGACTGTGGCGTGATCCAAGGAAACGCCTGTAGGAAGAAAAAGGATGCATTCC CTACAGATTTTTGGAGAAAGGATTTCTGAGGAGTGTGTGATGTGTTTCCATATATCTATATCCATAACT CTGATTATGAATACAGATATAAGAAATACAAAAGTTTAAAAAGCTCACATAGATATGACTTGGGAAGTG ACACCAGTTCTTTTAAAATAAATTTGTATGCTCAATTATTTTGCATTTTTTCTTTTTCCCCAATAAATT GTTGTGTGTGCTTTCTAAATAATAATAAAACAACAGGGTTTTTTTCCAGAA 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_175611.3 |
Synonyms | EAA3; EEA3; GLR5; GluK1; gluR-5; GLUR5 |
Summary | Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. The subunit encoded by this gene is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to alter the properties of ion flow. Alternative splicing, resulting in transcript variants encoding different isoforms, has been noted for this gene. [provided by RefSeq, Jul 2008] |
Locus ID | 2897 |
MW | 12.7 |
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