CACNG3 (NM_006539) Human 3' UTR Clone
CAT#: SC207415
3' UTR clone of calcium channel voltage-dependent gamma subunit 3 (CACNG3) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CACNG3 (NM_006539) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_006539 |
Insert Size | 579 bp |
Sequence Data |
>SC207415 3’UTR clone of NM_006539
The sequence shown below is from the reference sequence of NM_006539. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCGGCCAACAGGCGCACCACGCCCGTCTGAACTGACCTCTGACCTCTGCCCCACGCCCAGCACAGCCTT GGGGGAAGTGTACAGAGATGTCTCTGAGGTTGCATGGCATGGTCCTTGTGATGGTATTACTTTTTACAA AGAATGAAACCAAATGGACTCAGCCCTCTCCCACATTTTCCCCTCACCCTCCAAGTCCTAACCCCTCCA TCCTCTCTAACTTTTCAAGCCAATCCCTTAATGTCATTCCTCTCTCTGTGTATCTGTGCCAGATGTTTT CCTTTCTTCCTTCTTTACTGGAAGGACCTCCACATTCTTCCCTCCTTGGAAGAGGACTTTACTAAAAGT CACAGGTGGTGGCCAGGGGGGATTTCCGAATCTCCATCAGGCGCGCTCATAGTTGTCCCCATTGTCTAC CCACACAAATCCTCAGGAAACCAACCACCGCCCAGGTGGCCCTGAGGGAGGCATTCACCTTTATGTGTT AGAAAAACATGACCAGAAATCAAAGATGTCAGAGCCCCGAAGCAGCTAATGTAATAAGCACTCATGTTA TTAAAGGTTTTGCCTTGTCGTAACCAA 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_006539.4 |
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. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family. This gene is a susceptibility locus for childhood absence epilepsy. [provided by RefSeq, Dec 2010] |
Locus ID | 10368 |
MW | 21.9 |
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