CACNA1A (NM_001127221) Human 3' UTR Clone
CAT#: SC215555
3`UTR clone of calcium channel voltage-dependent P/Q type alpha 1A subunit (CACNA1A) transcript variant 3 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | CACNA1A |
Synonyms | APCA; BI; CACNL1A4; CAV2.1; EA2; EIEE42; FHM; HPCA; MHP; MHP1; SCA6 |
ACCN | NM_001127221 |
Insert Size | 1602 bp |
Sequence Data |
>SC215555 3'UTR clone of NM_001127221
The sequence shown below is from the reference sequence of NM_001127221. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CGAGAGCACATGGCGCACCGGCAGTAGTTCCGTAAGTGGAAGCCCAGCCCCCTCAACATCTGGTACCAGC ACTCCGCGGCGGGGCCGCCGCCAGCTCCCCCAGACCCCCTCCACCCCCCGGCCACACGTGTCCTATTCCC CTGTGATCCGTAAGGCCGGCGGCTCGGGGCCCCCGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA GCAGGCGGTGGCCAGGCCGGGCCGGGCGGCCACCAGCGGCCCTCGGAGGTACCCAGGCCCCACGGCCGAG CCTCTGGCCGGAGATCGGCCGCCCACGGGGGGCCACAGCAGCGGCCGCTCGCCCAGGATGGAGAGGCGGG TCCCAGGCCCGGCCCGGAGCGAGTCCCCCAGGGCCTGTCGACACGGCGGGGCCCGGTGGCCGGCATCTGG CCCGCACGTGTCCGAGGGGCCCCCGGGTCCCCGGCACCATGGCTACTACCGGGGCTCCGACTACGACGAG GCCGATGGCCCGGGCAGCGGGGGCGGCGAGGAGGCCATGGCCGGGGCCTACGACGCGCCACCCCCCGTAC GACACGCGTCCTCGGGCGCCACCGGGCGCTCGCCCAGGACTCCCCGGGCCTCGGGCCCGGCCTGCGCCTC GCCTTCTCGGCACGGCCGGCGACTCCCCAACGGCTACTACCCGGCGCACGGACTGGCCAGGCCCCGCGGG CCGGGCTCCAGGAAGGGCCTGCACGAACCCTACAGCGAGAGTGACGATGATTGGTGCTAAGCCCGGGCGA GGTGGCGCCCGCCCGGCCCCCCACGCACCCCACGCACACACCCCACCCGAGGAGCCGCGCAGAGGCCGCG GGGGCCCAGCACAGAGGGCCCGGGAGAGGGCCAGCCGGGAGACCCCAGACTCTGGAGAGGCCAGGGCTGG GCCACAAGGGTGTCCCGCAGAGACCCTCGGCCAAAAGAGACCCTCCTGGGCAGCCACGGCGCCCCCCAAC CAGCCCCGATCCCCCCACCCACGACAGGGGCTCTCGGGTGGGAGGCAGGGAGCAGACAAACCACACAGCC AAGGGATTTGAATTAACTCAGCCATTTTTGGAGAACTTTGGGGAACATGAAAAAAAAAAAAAAAAAAAAA AAAAAAAACATTTTTAAAAGAAAAAACGGGGAGAAAAAAATAGCTTCTATTGATGAGTTTTATCATCTCA ATTGAATCTTTCCTTTCCCTGATGAAGACAGCTGGTGGCCGAGTGCGGCAAAGAAGCCAGAAGGAACCAG AATCCCAGTGCCCTACACCCACCACCAGACACACTCACACCCACACACGTTCTCAGACACACACAAGAGT GCTTGCCGGTTATACCAAACCCTACTATTACTGCCTGCAGAAATCAATTTAAAAAAATAATAATAACAAT AAACAATTTTAAAAAGGACAAAAAAATTAATGATTGAGAAAAGAGGCATTTTTTTCTGACATTTGGTCCT GCTTGAAACAACAAAAGAAGAAGAAAAACCCACCATCACCACCGATTCCTTTGCTTCTTTTTTCCTTTTT TCCTACCTTGTTTGAAAACCGTGGGCTTGGGACTGTGAATTATTGCATGACATTCAAAAAGA CGGACCGTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data | |
RefSeq | NM_001127221.1 |
Summary | 'Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas, the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1A subunit, which is predominantly expressed in neuronal tissue. Mutations in this gene are associated with 2 neurologic disorders, familial hemiplegic migraine and episodic ataxia 2. This gene also exhibits polymorphic variation due to (CAG)n-repeats. Multiple transcript variants encoding different isoforms have been found for this gene. In one set of transcript variants, the (CAG)n-repeats occur in the 3' UTR, and are not associated with any disease. But in another set of variants, an insertion extends the coding region to include the (CAG)n-repeats which encode a polyglutamine tract. Expansion of the (CAG)n-repeats from the normal 4-18 to 21-33 in the coding region is associated with spinocerebellar ataxia 6. [provided by RefSeq, Jul 2016]' |
Locus ID | 773 |
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