CACNG2 (NM_006078) Human 3' UTR Clone

Specifications

Product Data
Product Name	CACNG2 (NM_006078) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MRD10
ACCN	NM_006078
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC203825 3’UTR clone of NM_006078 The sequence shown below is from the reference sequence of NM_006078. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACAGCCAACCGCCGGACCACCCCCGTATAAAGACCGCGGGCCTCGCCAGAAGACCGCGGGAGGAGGGCG CGGTCCCCGGGGGCGGGGCGGGGCGGGGAGACCCAGACCCTCCGCTGGGAGACCTTCCAAAAGCAAAAA CAAAAAACAAAAAAAACAAAAAAACAAAAAACAAAAAAACACACACACACAAAAAAAGAGAAAAAACAT AACAAGTAAATTTTAAAAAAAAGAACAAAATATAAGAGGAACAAAGAAGCAAAACAACAGGAAATGTGG GAAAATATAAACGAGGGAAGAAAACAAACTTTAAAAAAAAGCGAGAGGGATAAAAAATTAAAAATAGAA AATAAATCTAAAAGAAAATGCATGATTTCCCATGTACCATTATTTTAACATTTAATAAAAATCAATTTA AATGAAAAAATAAAAGGGAACCAAGATAACATTAAAGCAAAAAAAAAAAAAATGAGAACAGAAAGGAAA GGGGATGTCCTTTGTATTTTTCAGGGTTTATGTTACTTTTTTTTTTTTTTTTTAACTCGGGGAGAGTTA CTTTTCTGTTCCCTTTAACCCCCAGCGGGCCCTGCCTCCCTGGGAGATTGGGGGGCGAGACTCAGGGGC CCTGGGGCCAGGTGAGCCTGCAGTCACTGCCAGGTCCCTGGAGCCCCTGGGTGGGTGCCCCAGGAACTC CAGGAAGGCTCAGAGCTCGAGCCGGCTCCGCCCAGCATTGATGGGGCAATCGTAGGCCTCCAGGTGACC GAGCCCTTGTCCCTCCTCTCCGTTAGGGTGCCTGGAGGGGGGTACACTTGGGGCTTGCCTGGCCCCAGG TTCCCAGTCCTTAATGCTCCTTAACCCACTGTGATGACTTCCTAGGCCTTGAGGAAAGGGAAGGAGAGG GGAGGCTGCCGGTGGCTTACCAAGATGCCGGAAACCCCGGAATCCTCAGGGTGAGCCTCTTGGGGTCAT GTCCCCAAGCTCCTGTCCTTGGGGTCAGGAGATGCCACCCCCCCCCCCGGGGGACATGAAACAGCTCTC CCTCCTCACCCCTCACCTCAGGGCCACCTGATGACCCTGGGGCGATGGTGGACCCCCTGACTCATAAGC CCCCCAGTCCCCTGGGAAGGGGGTTCATTGACCCTTTGGGGGTCCTTGGACTCACTGATGCCCCCTTGG GGCCCAGCGGGTTCAACAATGACACTGCAAAAAGGCTTCTTTTTACAAAAGAAAAAGGAAAAACAAGTG GTGATTTTTTTTTAATAAAAAAACCACAGACTATAAATAAATGTAAATACAAAATAAGTGGATTTACTT GCAAGAAAATCAGATAGTATTTTTCTTTTAATTCTTTTCCAGCTTTAAACTGTGAAAACAAAAAATGGG GCGGGGTGGGGGACTTAAACTTTAGCAGGGAACTTGTAAAGAAAAAAAAAACAGAAAACGAATATACAA ATCCATTTACAAAAACAAAGCAAAACCGTTGTGAGAGGTGAGAGCTGGGCTTGAAGGTTGGAGGGAGTA GCGGAAGGTCCCAGTGAGCTGCAGGGGGTCTCTGTGATGGAAAGGTGGCTTCCTCAGACAAGGAAGGTG CTGCGAATGGGGGAAGACAGAATCCAACAAAGAAAGAGACCACACACCCCACACGCACACAGGCACGTT CACACACACATACACAGTCCACTTAGCCCAGCACTGCAGTCACTCACAGGGACACACTCAGTCTCAACC CTTCCATCCCATACACGGCCAGGGGCGTGGCTCAAAGGAAATTGACTCATGCCCTCCAAAGCCATGGAC GACAACAACTCCACACTGGCCTTTGTGTTCATTCACAACCTCCCAACAGAGCATACACATGAACACACA CATGCACACATACCCACACACGCACACATACCCACACACACACACACACCACTCGCATGCATGGGAAGG GCACCCGTCTAGAATCCAGGACTGGATTCCGGAATTCCTTGCTGCATGGCCTCTCTGGGCCTTAATTT 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_006078.5
Synonyms	MRD10
Summary	The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. The AMPA subtype of ionotropic glutamate receptors are ligand gated ion channels that are typically activated by glutamate released from presynaptic neuron terminals and mediate fast neurotransmission in excitatory synapses. TARPs thus play an important role in synaptic plasticity, learning and memory. Mutations in this gene cause an autosomal dominant form of cognitive disability. [provided by RefSeq, Jul 2017]
Locus ID	10369
MW	74.4

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