GJA1 (NM_000165) Human 3' UTR Clone
CAT#: SC216210
3`UTR clone of gap junction protein alpha 1 43kDa (GJA1) 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 | GJA1 |
Synonyms | AVSD3; CMDR; CX43; EKVP; EKVP3; GJAL; HLHS1; HSS; ODDD; PPKCA |
ACCN | NM_000165 |
Insert Size | 1726 |
Sequence Data |
>SC216210 3'UTR clone of NM_000165
The sequence shown below is from the reference sequence of NM_000165. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCCTGATGACCTGGAGATCTAGATACAGGCTTGAAAGCATCAAGATTCCACTCAATTGTGGAGAAGAAAA AAGGTGCTGTAGAAAGTGCACCAGGTGTTAATTTTGATCCGGTGGAGGTGGTACTCAACAGCCTTATTCA TGAGGCTTAGAAAACACAAAGACATTAGAATACCTAGGTTCACTGGGGGTGTATGGGGTAGATGGGTGGA GAGGGAGGGGATAAGAGAGGTGCATGTTGGTATTTAAAGTAGTGGATTCAAAGAACTTAGATTATAAATA AGAGTTCCATTAGGTGATACATAGATAAGGGCTTTTTCTCCCCGCAAACACCCCTAAGAATGGTTCTGTG TATGTGAATGAGCGGGTGGTAATTGTGGCTAAATATTTTTGTTTTACCAAGAAACTGAAATAATTCTGGC CAGGAATAAATACTTCCTGAACATCTTAGGTCTTTTCAACAAGAAAAAGACAGAGGATTGTCCTTAAGTC CCTGCTAAAACATTCCATTGTTAAAATTTGCACTTTGAAGGTAAGCTTTCTAGGCCTGACCCTCCAGGTG TCAATGGACTTGTGCTACTATATTTTTTTATTCTTGGTATCAGTTTAAAATTCAGACAAGGCCCACAGAA TAAGATTTTCCATGCATTTGCAAATACGTATATTCTTTTTCCATCCACTTGCACAATATCATTACCATCA CTTTTTCATCATTCCTCAGCTACTACTCACATTCATTTAATGGTTTCTGTAAACATTTTTAAGACAGTTG GGATGTCACTTAACATTTTTTTTTTGAGCTAAAGTCAGGGAATCAAGCCATGCTTAATATTTAACAATCA CTTATATGTGTGTCGAAGAGTTTGTTTTGTTTGTCATGTATTGGTACAAGCAGATACAGTATAAACTCAC AAACACAGATTTGAAAATAATGCACATATGGTGTTCAAATTTGAACCTTTCTCATGGATTTTTGTGGTGT GGGCCAATATGGTGTTTACATTATATAATTCCTGCTGTGGCAAGTAAAGCACACTTTTTTTTTCTCCTAA AATGTTTTTCCCTGTGTATCCTATTATGGATACTGGTTTTGTTAATTATGATTCTTTATTTTCTCTCCTT TTTTTAGGATATAGCAGTAATGCTATTACTGAAATGAATTTCCTTTTTCTGAAATGTAATCATTGATGCT TGAATGATAGAATTTTAGTACTGTAAACAGGCTTTAGTCATTAATGTGAGAGACTTAGAAAAAATGCTTA GAGTGGACTATTAAATGTGCCTAAATGAATTTTGCAGTAACTGGTATTCTTGGGTTTTCCTACTTAATAC ACAGTAATTCAGAACTTGTATTCTATTATGAGTTTAGCAGTCTTTTGGAGTGACCAGCAACTTTGATGTT TGCACTAAGATTTTATTTGGAATGCAAGAGAGGTTGAAAGAGGATTCAGTAGTACACATACAACTAATTT ATTTGAACTATATGTTGAAGACATCTACCAGTTTCTCCAAATGCCTTTTTTAAAACTCATCACAGAAGAT TGGTGAAAATGCTGAGTATGACACTTTTCTTCTTGCATGCATGTCAGCTACATAAACAGTTTTGTACAAT GAAAATTACTAATTTGTTTGACATTCCATGTTAAACTACGGTCATGTTCAGCTTCATTGCATGTAATGTA GACCTAGTCCATCAGATCATGTGTTCTGGAGAGTGTTCTTTATTCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_000165.3 |
Summary | This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014] |
Locus ID | 2697 |
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