CHRND (NM_000751) Human 3' UTR Clone
CAT#: SC201945
3`UTR clone of cholinergic receptor nicotinic delta (CHRND) 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 | CHRND |
Synonyms | ACHRD; CMS2A; CMS3A; CMS3B; CMS3C; FCCMS; SCCMS |
ACCN | NM_000751 |
Insert Size | 191 bp |
Sequence Data |
>SC201945 3'UTR clone of NM_000751
The sequence shown below is from the reference sequence of NM_000751. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CTACTCCTACAACGTGCAGGACAAGCGCTTCATCTAGGGTGGGCCTGTTGGGGAGCCAGGAGACAGCAGG GTCTGAGAGAGGAGCCACAGTCCCTAATGACACCCACTCCTAGCCCTGAGGCTCGTGCCCCTCAGACTGG GGAAGAGTCCAAGGAAGGGAGGGAGCAGCCACTCCTCAATGCTCAATGGCT 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). |
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_000751.1 |
Summary | 'The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]' |
Locus ID | 1144 |
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