CNG1 (CNGA1) (NM_000087) Human 3' UTR Clone
CAT#: SC206081
3' UTR clone of cyclic nucleotide gated channel alpha 1 (CNGA1) transcript variant 2 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 | CNG1 (CNGA1) (NM_000087) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CNCG; CNCG1; CNG-1; CNG1; RCNC1; RCNCa; RCNCalpha; RP49 |
ACCN | NM_000087 |
Insert Size | 474 bp |
Sequence Data |
>SC206081 3’UTR clone of NM_000087
The sequence shown below is from the reference sequence of NM_000087. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCGGAAAGTGGGCCCATCGACTCTACATAGAACCGAAAAGCTGGTCATTAACAGGGACATGCCTCATGA TCCTTTTGATCCTATGACTGACATCAACTAAAATTTAAAAGAAGAGGAAGACTCAGTTGGGAAATTTTT CCATGAGGAAAATGTGCTTTGGTGCAAGGTACAAGGCCCACACCCTCTCTGAGAGATACTATGATTAAA AAAGCTTTATATCTTGGGATTTTTCACAACTGATAATGTGCAAAGATATAAACTGATTAACTTGTCAGT GTCTGTATTTTCTGATTTTTTCACATACGCTCATTTTATGTAATATTCTTCATAAAAATGAATAAGTAG CCCTCACTTTCATGCCATTTCCATTGTTGAGTGAAGCGTATTTGAAGTAACTGAGAATTACCATGTACA TCATATTTGGGATAACATTTTTAAAAATTAGACTGCAATAAAGTAAAATTAATTATGCAA 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_000087.5 |
Synonyms | CNCG; CNCG1; CNG-1; CNG1; RCNC1; RCNCa; RCNCalpha; RP49 |
Summary | The protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Multiple transcript variants have been found for this gene. [provided by RefSeq, Oct 2019] |
Locus ID | 1259 |
MW | 18.2 |
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